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Calculations In Chemistry Modules 13 to 16 A Note to the Student The focus of these lessons is to provide methods will help you to solve numeric calculations in first-year chemistry. This is only one part of a course in chemistry, but it is often the most challenging. Problem Notebook: The purchase of a spiral problem notebook is suggested as a place to write your work when solving the problems in these lessons. A notebook that has graphpaper as its pages will be especially helpful. Choosing a Calculator: As you do problems in these lessons (and assigned homework) that require a calculator, use the same calculator that you will be allowed to use during quizzes and tests. Calculators have many different labels and placements of keys. It is advisable to practice the rules and keys for a calculator before quizzes and tests. Many courses will not allow the use of a graphing calculator or other types of calculators with extensive memory during tests. If a type of calculator is specified for your course, buy two if possible. When one becomes broken or lost, you will have a familiar backup if the bookstore is sold out later in the term. If no type of calculator is specified for your course, any inexpensive calculator with a 1/x or x-1 , yx or ^ , log or 10x , and ln functions will be sufficient for most calculations in introductory chemistry courses. When to Do the Lessons: You will receive the maximum benefit from these lessons by completing each topic before it is addressed in your class. Where to Start and Lesson Sequence: The order of these lessons may not always match the order in which topics are covered in your course. If you are using these modules as part of a course, you should do the lessons in the order in which they are assigned by your instructor. If you are using these lessons on your own to assist with a course, begin by • Determining the topics that will be covered on your next graded assignment: problem set, quiz, or test. • Find that topic in the Table of Contents. • Download the modules that precede and include the topics. • Find the prerequisite lessons for the topic, listed at the beginning of the module or lesson. Print the needed lessons. Do the prerequisites, then the topics related to your next graded assignments. • Follow the instructions on “How to Use These Lessons” on page 1. If you begin these lessons after the start of your course, when time permits, review prior topics in these lessons as needed, starting with Module 1. You will need all of these introductory modules for later topics -- and for your final exam. Check back for updates at www.ChemReview.Net . ©2008 ChemReview.net v. f9 Page i Table of Contents — Volume 1 How to Use These Lessons ............................................................................................... 1 Module 1 – Scientific Notation ........................................................................................ 2 Lesson 1A: Lesson 1B: Lesson 1C: Moving the Decimal ..............................................................................................3 Calculations Using Exponential Notation ..........................................................7 Tips for Complex Calculations...........................................................................12 Module 2 – The Metric System ......................................................................................19 Lesson 2A: Lesson 2B: Lesson 2C: Lesson 2D: Metric Fundamentals...........................................................................................20 Calculations With Units ......................................................................................25 Metric Prefix Formats ..........................................................................................27 Cognitive Science -- and Flashcards ..................................................................30 Module 3 – Significant Figures...................................................................................... 35 Lesson 3A: Lesson 3B: Lesson 3C: Rules for Significant Figures...............................................................................35 Sig Figs -- Special Cases.......................................................................................37 Sig Fig Summary and Practice............................................................................41 Module 4 – Conversion Factors......................................................................................44 Lesson 4A: Lesson 4B: Lesson 4C: Lesson 4D: Lesson 4E: Conversion Factor Basics ....................................................................................44 Single Step Conversions......................................................................................48 Multi-Step Conversions.......................................................................................51 English/Metric Conversions ..............................................................................53 Ratio Unit Conversions .......................................................................................57 Module 5 – Word Problems ............................................................................................62 Lesson 5A: Lesson 5B: Lesson 5C: Lesson 5D: Lesson 5E: Lesson 5F: Lesson 5G: Answer Units -- Single Or Ratio?.......................................................................62 Mining The DATA ...............................................................................................64 Solving For Single Units......................................................................................67 Finding the Given .................................................................................................72 Some Chemistry Practice ....................................................................................75 Area and Volume Conversions ..........................................................................77 Densities of Solids: Solving Equations .............................................................82 Module 6 – Atoms, Ions, and Periodicity..................................................................... 89 Lesson 6A: Lesson 6B: Lesson 6C: Lesson 6D: Lesson 6E: Atoms.....................................................................................................................89 The Nucleus, Isotopes, and Atomic Mass.........................................................94 Elements, Compounds, and Formulas ............................................................101 The Periodic Table..............................................................................................106 A Flashcard Review System .............................................................................110 Module 7 – Writing Names and Formulas.................................................................113 Lesson 7A: Lesson 7B: Lesson 7C: Naming Elements and Covalent Compounds ...............................................113 Naming Ions .......................................................................................................118 Names and Formulas for Ionic Compounds..................................................128 ©2008 ChemReview.net v. f9 Page ii Module 8 – Grams and Moles...................................................................................... 142 Lesson 8A: Lesson 8B: Lesson 8C: Lesson 8D: The Mole ............................................................................................................. 142 Grams Per Mole (Molar Mass)......................................................................... 144 Converting Between Grams and Moles ......................................................... 146 Converting Particles, Moles, and Grams........................................................ 150 Module 9 – Mole Applications .................................................................................... 155 Lesson 9A: Lesson 9B: Lesson 9C: Lesson 9D: Fractions and Percentages................................................................................ 155 Empirical Formulas........................................................................................... 157 Empirical Formulas from Mass or % Mass .................................................... 158 Mass Fraction, Mass Percent, Percent Composition..................................... 163 Module 10 – Balanced Equations and Stoichiometry.............................................. 172 Lesson 10A: Lesson 10B: Lesson 10C: Lesson 10D: Lesson 10E: Lesson 10F: Chemical Reactions and Equations................................................................. 172 Balancing Equations.......................................................................................... 175 Using Coefficients -- Molecules to Molecules ............................................... 180 Mole to Mole Conversions ............................................................................... 182 Stoichiometry ..................................................................................................... 185 Limiting Reactants and Reactants in Excess .................................................. 192 Module 11 – Molarity .................................................................................................... 200 Lesson 11A: Lesson 11B: Lesson 11C: Lesson 11D: Lesson 11E: Lesson 11F: Lesson 11G: Ratio Unit Review ............................................................................................. 200 Word Problems With Ratio Answers ............................................................. 201 Molarity .............................................................................................................. 207 Conversions and Careers ................................................................................. 213 Units and Dimensions ..................................................................................... 216 Ratios Versus Two Related Amounts ............................................................ 221 Solving Problems With Parts .......................................................................... 228 Module 12 – Molarity Applications............................................................................ 238 Lesson 12A: Lesson 12B: Lesson 12C: Dilution .............................................................................................................. 238 Ion Concentrations ............................................................................................ 247 Solution Stoichiometry ..................................................................................... 254 Module 13 – Ionic Equations and Precipitates ........................................................ 265 Lesson 13A: Lesson 13B: Lesson 13C: Lesson 13D: Predicting Solubility for Ionic Compounds .................................................. 265 Total and Net Ionic Equations ......................................................................... 269 Predicting Precipitation.................................................................................... 273 Precipitate and Gravimetric Calculations ...................................................... 280 Module 14 – Acid-Base Neutralization ...................................................................... 287 Lesson 14A: Lesson 14B: Lesson 14C: Lesson 14D: Lesson 14E: Ions in Acid-Base Neutralization .................................................................... 287 Balancing Hydroxide Neutralization ............................................................. 291 Acid-Hydroxide Neutralization Calculations ............................................... 298 Neutralization Calculations in Parts............................................................... 304 Carbonate Neutralization................................................................................. 311 ©2008 ChemReview.net v. f9 Page iii Module 15 – Redox Reactions ......................................................................................319 Lesson 15A: Lesson 15B: Lesson 15C: Lesson 15D: Lesson 15E: Oxidation Numbers ...........................................................................................319 Balancing Charge ...............................................................................................324 Balancing Redox Using Oxidation Numbers .................................................328 Oxidizing and Reducing Agents..................................................................... 330 Redox Stoichiometry......................................................................................... 334 Module 16 – Half-Reaction Balancing........................................................................338 Lesson 16A: Lesson 16B: Lesson 16C: Lesson 16D: Constructing Half-Reactions – The CA-WHe! Method ................................338 Balancing By Adding Half-Reactions..............................................................344 Separating Redox Into Half-Reactions ............................................................347 Balancing Redox With Spectators Present......................................................350 Volume 2 Module 17 – Ideal Gases ...............................................................................................357 Lesson 17A: Lesson 17B: Lesson 17C: Lesson 17D: Lesson 17E: Lesson 17F: Lesson 17G: Gas Fundamentals..............................................................................................357 Gases at STP........................................................................................................361 Complex Unit Cancellation...............................................................................366 The Ideal Gas Law and Solving Equations.....................................................371 Density, Molar Mass, and Choosing Equations.............................................375 Using the Combined Equation .........................................................................382 Gas Law Summary and Practice ......................................................................388 Module 18 – Gas Labs, Gas Reactions ........................................................................392 Lesson 18A: Lesson 18B: Lesson 18C: Lesson 18D: Charles’ Law; Graphing Direct Proportions...................................................392 Boyle’s Law; Graphs of Inverse Proportions..................................................399 Avogadro’s Hypothesis; Gas Stoichiometry ..................................................403 Dalton’s Law of Partial Pressures ....................................................................410 Module 19 – Graphing...................................................................................................417 Lesson 19A: Lesson 19B: Lesson 19C: Lesson 19D: Lesson 19E: Lesson 19F: Graphing Fundamentals ...................................................................................417 The Specific Equation for a Line ......................................................................428 Graphing Experimental Data ...........................................................................435 Deriving Equations From Linear Data ............................................................445 Linear Equations Not Directly Proportional ..................................................456 Graphing Inverse Proportions..........................................................................463 Module 20 – Phases Changes and Energy..................................................................472 Lesson 20A: Lesson 20B: Lesson 20C: Lesson 20D: Lesson 20E: Phases and Phase Changes ...............................................................................472 Specific Heat Capacity and Equations ............................................................485 Water, Energy, and Consistent Units ..............................................................492 Calculating Joules Using Unit Cancellation ...................................................496 Calorimetry .........................................................................................................502 ©2008 ChemReview.net v. f9 Page iv Module 21 – Heats Of Reaction (ΔH) ......................................................................... 510 Lesson 21A: Lesson 21B: Lesson 21C: Exo- And Endothermic Reactions .................................................................. 510 Heats of Formation and Element Formulas................................................... 514 Adding ΔH Equations (Hess’s Law)............................................................... 521 Module 22 – Light and Spectra ................................................................................... 531 Lesson 22A: Lesson 22B: Lesson 22C: Lesson 22D: Lesson 22E: Waves ................................................................................................................. 531 Planck's Constant ............................................................................................. 536 DeBroglie’s Wavelength .................................................................................. 544 The Hydrogen Atom Spectrum ....................................................................... 549 Quantum Mechanics ........................................................................................ 555 Module 23 – Electron Configuration .......................................................................... 560 Lesson 23A: Lesson 23B: Lesson 23C: Lesson 23D: The Multi-Electron Atom ................................................................................. 560 Abbreviated Electron Configurations............................................................. 564 The Periodic Table and Electron Configuration ........................................... 570 Electron Configurations: Exceptions and Ions ............................................ 574 Module 24 – Bonding ................................................................................................... 579 Lesson 24A: Lesson 24B: Lesson 24C: Lesson 24D: Lesson 24E: Lesson 24F: Lesson 24G: Lesson 24H: Covalent Bonds.................................................................................................. 579 Molecular Shapes and Bond Angles ............................................................... 584 Electronegativity................................................................................................ 592 Molecular Polarity............................................................................................. 597 Solubility............................................................................................................. 602 Double and Triple Bonds ................................................................................. 606 Ion Dot Diagrams .............................................................................................. 612 Orbital Models for Bonding ............................................................................. 614 Volume 3 Module 25 – Kinetics ..................................................................................................... 619 Lesson 25A: Lesson 25B: Lesson 25C: Lesson 25D: Lesson 25E: Lesson 25F: Lesson 25G: Lesson 25H: Kinetics Fundamentals .................................................................................... 619 Rate Laws ........................................................................................................... 623 Integrated Rate Law --Zero Order .................................................................. 633 Logarithms ........................................................................................................ 641 Integrated Rate Law -- First Order.................................................................. 656 Reciprocal Math................................................................................................. 666 Integrated Rate Law -- Second Order ............................................................. 671 Half-Life.............................................................................................................. 678 Module 26 – Equilibrium.............................................................................................. 687 Lesson 26A: Lesson 26B: Lesson 26C: Lesson 26D: Lesson 26E: Le Châtelier’s Principle..................................................................................... 688 Powers and Roots of Exponential Notation................................................... 700 Equilibrium Constants...................................................................................... 710 K Values ............................................................................................................. 716 Kp Calculations .................................................................................................. 720 ©2008 ChemReview.net v. f9 Page v Lesson 26F: Lesson 26G: Lesson 26H: Lesson 26I: Lesson 26J: The Rice Moles Table.........................................................................................726 K Calculations From Initial Concentrations ...................................................734 Q: The Reaction Quotient..................................................................................740 Calculations Using K and Q..............................................................................743 Solving Quadratic Equations............................................................................749 Module 27 – Acid-Base Fundamentals .......................................................................760 Lesson 27A: Lesson 27D: Acid-Base Math Review ....................................................................................760 Kw Calculations: H+ and OH─ .......................................................................763 Strong Acid Solutions........................................................................................767 The [OH─] in Strong Acid Solutions...............................................................770 Lesson 27E: Strong Base Solutions ........................................................................................774 Lesson 27F: The pH System ...................................................................................................776 Lesson 27B: Lesson 27C: Module 28 – Weak Acids and Bases............................................................................786 Lesson 28A: Lesson 28B: Lesson 28C: Lesson 28D: Lesson 28E: Lesson 28F: Lesson 28G: Lesson 28H: Weak Acids and Ka Expressions ......................................................................786 Ka Math................................................................................................................791 Ka Calculations ...................................................................................................794 Solving Ka Using the Quadratic Formula .......................................................805 Weak Bases and Kb Calculations......................................................................808 Polyprotic Acid Calculations............................................................................819 Brønsted-Lowry Definitions .............................................................................824 Which Acid-Base Reactions Go? ......................................................................830 Module 29 – Salts and Buffers .....................................................................................838 Lesson 29A: Lesson 29B: Lesson 29C: Lesson 29D: Lesson 29E: Lesson 29F: The Acid-Base Behavior of Salts.......................................................................838 Calculating the pH of a Salt Solution .............................................................846 Salts That Contain Amphoteric Ions ...............................................................860 Acid-Base Common Ions, Buffers ....................................................................854 Buffer Equations.................................................................................................860 Buffer Calculations.............................................................................................865 Additional topics and resources are available online at www.ChemReview.Net . ••••• ©2008 ChemReview.net v. f9 Page vi Module 13 — Ionic Equations and Precipitates Module 13 — Ionic Equations and Precipitates Pretests: On any of these lessons, if you think you know the topic, try the last problem in the lesson. If you can do that problem, you may skip the lesson. Lesson 13A: Predicting Solubility for Ionic Compounds Prerequisites: If you have any problems translating between the names, solid formulas, and separated formulas for ionic compounds during Module 13, review your Lesson 7C and your ion name and formula flashcards from Lesson 7B. * * * * * Solubility Terminology All ionic compounds dissolve to some extent in water, and some dissolve to a substantial extent. Solubility for ionic compounds is temperature dependent. Some dissolve to a greater extent in warmer solvents, some dissolve less, and some ionic compounds have borderline solubility at room temperature. Those messy realities aside, most ion combinations can generally be classified as soluble or insoluble in water. A commonly accepted definition is • if 0.10 moles or more of a solid dissolve per liter of solution at room temperature, the solid is termed soluble; • if the solid dissolves less than 0.10 moles per liter, it is considered either slightly soluble or insoluble. Most introductory chemistry courses ask that you memorize a set of solubility rules that will allow you to predict the solubility of many ion combinations. Although there are some patterns to solubility based on the Periodic Table, there are limited simple rules. The solubility scheme on the following page will cover most ions customarily assigned. However, • if your course requires that you memorize a particular chart, memorize it instead of this one. • If you are allowed to consult a particular solubility chart on quizzes and tests, use it in place of this one. • If the following chart conflicts in its predictions from a chart you are assigned in your class, use the one that you are assigned. ©2008 ChemReview.net v. f9 Page 265 Module 13 — Ionic Equations and Precipitates A Solubility Scheme The scheme below is hierarchical: higher rules take precedence over those beneath them. To predict the solubility of ion combinations, apply the rules in order from the top. If only one ion of the two in a compound is in this table, you may presume that the compound will follow the rule for the ion that is shown. (This will not always be accurate, but is a best guess. With solubility, there are exceptions.) Positive Ions Negative Ions ─ ─ ─ ─ 1. (alkali metals)+ , NH4+ NO3 , CH3COO , ClO3 ; ClO4 Soluble (nitrate, acetate, chlorate, perchlorate) 2. Pb2+ , Hg22+ , Ag+ CO32─ , PO43─ , S2─ , CrO42─ Insoluble 3. Cl─ , Br─ , I─ (except Cu+) Soluble 4. Ba2+ (except OH─) OH─ (except Ba2+ , Sr2+, Ca2+) Insoluble 5. SO42─(except Sr2+, Ca2+) Soluble Exceptions include: Column 2 sulfides and aluminum sulfide decompose in water. CH3COOAg, Ag2SO4 and Hg2SO4 are moderately soluble. Memorization Tips 1. Most people best recall what they hear repeatedly (especially if it rhymes). You may want to recite the ion names in a series, as well as write them. 2. Notice the patterns in the last column, and in the empty boxes. 3. Focus especially on the rules near the top. In this scheme, the higher the rule, the more often it will be used. Using the Scheme to Make Predictions In using any solubility scheme, if you are unsure of the ions in a compound, you should write out the separated formula that shows the ion charges. Atoms that have two possible charges, such as Cu+ and Cu2+, can have differing solubilities. Let’s try a few predictions. Q. For the questions below, use the solubility scheme of your choice. Write your answer and your reason. 1. Is Ba(NO3)2 soluble? 2. Is PbCl2 soluble or insoluble? 3. Is Hg(NO3)2 soluble or insoluble? * * * * * ©2008 ChemReview.net v. f9 Page 266 Module 13 — Ionic Equations and Precipitates Answers 1. Yes. Ba(NO3)2 Æ Ba2+ + 2 NO3─ , and all nitrates are soluble. 2. PbCl2 Æ Pb2+ + 2 Cl─ . Pb2+ ion by Rule 2 is insoluble. Chloride ion in Rule 3 is soluble, but rule 2 takes precedence. PbCl2 is insoluble. 3. Hg(NO3)2 Æ Hg2+ + 2 NO3─ . The above solubility scheme makes no specific predictions for Hg2+, the mercuric [mercury (II)] ion, but based on Rule 1 that all nitrates are soluble, predict soluble. If only one ion in a pair is in the table, base your prediction on the rule for that ion. Practice If you are required to memorize solubility rules, do so before you do the practice below. To be useful, practice should be treated as a test (but one that you grade). Whenever there are rules you need to memorize for an assignment, quiz, or test, try writing them at the top of your assignment at the beginning. 1. Write your solubility scheme from memory. 2. Label the ion combinations as soluble or insoluble, and state a reason for your prediction. Check your answers after each one or two parts. a. K+ + Br─ b. Sr2+ + Cl─ c. Ca2+ + CO32─ d. Ag+ + CrO42─ 3. Write the separated ions for these combinations, then label the ion combination as soluble or insoluble, and state a reason for your prediction. (If you are using a different scheme, your reason may differ, but your answer will probably be the same.) Do every other part, and check your answers frequently. Do more if you need more practice. If you have trouble writing the separated ions, redo Lessons 7B and 7C. a. Lead (II) Bromide Æ Pb2+ + 2 Br─ ; Insoluble -- Rule 2 for Pb2+ (example) b. Barium Carbonate Æ c. Sodium Hydroxide Æ d. SrBr2 Æ ©2008 ChemReview.net v. f9 Page 267 Module 13 — Ionic Equations and Precipitates e. Silver nitrate Æ f. Ammonium hydroxide Æ g. Fe3(PO4)2 Æ h. Pb(CH3COO)2 Æ i. NiCl2 Æ j. BaSO4 Æ k. RbBr Æ l. Fe2S3 Æ 4. Which ions in combination with Pb2+ are soluble compounds? 5. Are all nitrates soluble? Are all phosphates insoluble? Answers These answers are based on the solubility scheme above. You will have different rules if you use a different scheme, but you should have the same answer in most cases, and a similar reason. 2. a. K+ + Br─ Soluble. Rule 1, first column metal ions are always soluble b. Sr2+ + Cl─ Soluble. Rule 3, chloride c. Ca2+ + CO32─ Insoluble. Rule 2, carbonates (if only one ion is in table, use it) d. Ag+ + CrO42─ Insoluble. Rule 2, chromate ion 3. b. Barium Carbonate Æ Ba2+ + CO32─ Insoluble by Rule 2 for carbonates c. Sodium Hydroxide Æ Na+ + OH─ Soluble by Rule 1 for alkali-metal ions d. SrBr2 Æ Sr2+ + 2 Br─ Soluble by Rule 3 for bromides e. Silver nitrate Æ Ag+ + NO3─ Soluble by Rule 1 for nitrates f. Ammonium hydroxide Æ NH4+ + OH─ Soluble by Rule 1 for ammonium ion g. Fe3(PO4)2 Æ 3 Fe2+ + 2 PO43─ Insoluble by Rule 2 for phosphate ions h. Pb(CH3COO)2 Æ Pb2+ + 2 CH3COO─ Soluble by Rule 1 for acetates i. NiCl2 Æ Ni2+ + 2 Cl─ Soluble by Rule 3 for chlorides ©2008 ChemReview.net v. f9 Page 268 Module 13 — Ionic Equations and Precipitates BaSO4 Æ Ba2+ + SO42─ Insoluble by Rule 4 for barium ions k. RbBr Æ Rb+ + Br─ Soluble by Rule 1 for alkali-metal ions j. l. Fe2S3 Æ 2 Fe3+ + 3 S2─ Insoluble by Rule 2 for sulfide ions 4. Which ions in combination with Pb2+ would make soluble compounds? Nitrate, acetate, chlorate, and perchlorate. 5. Are all nitrates soluble? YES. That is a rule used frequently. Are all phosphates insoluble? NO. Alkali-metal and ammonium-ion phosphates are soluble. * * * * * Lesson 13B: Total and Net Ionic Equations Prerequisites: Lessons 7C, 10B, and 13A. * * * * * Mixing Ions When solutions of different ions are mixed, chemical reactions can occur. One type of reaction is precipitation. When solutions of different soluble ionic compounds are mixed, the ions may “trade partners:” new combinations of positive and negative ions are possible. If a new combination is possible that is insoluble in water, it will precipitate: it will form a cloud of solid particles in the solution that sink to the bottom. For example, when a 0.1 M solution of sodium chloride (table salt) is mixed with a 0.1 M solution of silver nitrate, a bright white cloud immediately forms. Solid particles from the cloud slowly settle to the bottom of the solution. Over time, in light, the surface of the solid slowly turns grey. The precipitate formed is silver chloride (AgCl), a compound that reacts with light. The total ionic equation for this reaction is Na+(aq) + Cl─(aq) + Ag+(aq) + NO3─(aq) Æ AgCl(s) + Na+(aq) + NO3─(aq) The (aq) is an abbreviation for aqueous, which means dissolved in water. The (s) abbreviates solid. Note that the sodium and nitrate ions did not change in the reaction. Ions that are present, but do not change during a reaction, are called spectator ions. In total ionic equations, the spectator ions are included on both sides, and they will be the same on both sides. Including the spectators helps us to see all of the reactant and product compounds. However, as in math equations, terms that are the same on both sides of an equation can be cancelled. Canceling the spectators gives the net ionic equation, which shows only the particles that changed in the reaction. For the reaction above, cancel the spectators and write the net ionic equation. * * * * * ©2008 ChemReview.net v. f9 Page 269 Module 13 — Ionic Equations and Precipitates Ag+(aq) + Cl─(aq) Practice A: Æ AgCl(s) Do Part a on each of these. If you need more practice, do Part b. 1. For these total ionic equations, circle the precipitate, cross out the spectators, and write the net ionic equation. a. Pb2+(aq) + 2 NO3― (aq) + Cu2+(aq) + 2 Cl―(aq) Æ Cu2+(aq) + 2 NO3―(aq) + PbCl2(s) b. 6 Na+(aq) + 2 PO43―(aq) + 3 Mg2+(aq) + 3 SO42―(aq) Æ Mg3(PO4)2(s) + 6 Na+(aq) + 3 SO42―(aq) 2. Balance these precipitation equations. (For rules, see Lesson 10B). a. Fe(NO3)3(aq) + NaOH(aq) Æ Fe(OH)3(s) + NaNO3(aq) b. Ca(NO3)2(aq) + K3PO4(aq) Æ KNO3(aq) + Ca3(PO4)2(s) 3. Formulas for “aqueous solids,” such as in Problem 2 above, are often written to represent ionic solids dissolved in a solution. In reality, however, if an ionic solid dissolves in water, its ions will separate in the solution. Total and net ionic equations show separated-ion formulas -- unless the ions precipitate. Re-write the balanced equations for 2a and 2b using separated-ion formulas. This will be the total ionic equation for each reaction. 4. Write the net ionic equations for the reactions in 2a and 2b. Balancing Total Ionic Equations For precipitation reactions, you will often be asked to balance a total ionic equation. To balance properly, you must first balance each of the reactant and product formulas for charge, then balance again to account for ratios of reaction. In the following equation, the brackets show the original ion combinations on the left and the new possible combinations on the right. [ Ca2+ + NO3― ] + [ K+ + PO43―] Æ Ca3(PO4)2(s) + [ K+ + NO3― ] To balance, first add coefficients inside the brackets so that the charges are balanced for each substance formula, and then check your answer below. (For reactions conducted in aqueous solutions, if no state is shown, assume (aq).) * * * * * [ 1 Ca2+ + 2 NO3― ] + [ 3 K+ + 1 PO43―] Æ Ca3(PO4)2(s) + [ 1 K++ 1 NO3― ] Now add coefficients in front of the brackets so that all of the atoms balance. * * * * * To form the precipitate, 3 calcium atoms and 2 phosphate ions are needed, so: 3 [1 Ca2+ + 2 NO3―] + 2 [3 K+ + 1 PO43―] Æ 1 Ca3(PO4)2(s) + 6 [1 K+ + 1 NO3―] ©2008 ChemReview.net v. f9 Page 270 Module 13 — Ionic Equations and Precipitates Write the total ionic equation by removing the brackets. Check that the total ionic equation is balanced for atoms. In total ionic equations, check also that the charges on each side total to zero as well. * * * * * 3 Ca2+ + 6 NO3― + 6 K+ + 2 PO43― Æ 1 Ca3(PO4)2(s) + 6 K+ + 6 NO3― Check: 3 Ca, 6 N, 6K, 2 P, 26 O on both sides. Zero net charge on both sides. Balanced. Practice B: Re-write these equations as balanced total ionic equations. SO42― ] + 1. [ K+ + 2. [ Fe2+ + Br ― ] + [ [ Sr2+ + NO3― ] Æ Na+ + PO43― ] Æ [ SrSO4(s) + Na+ + [ K+ + Br― ] + NO3― ] Fe3(PO4)2(s) Balancing Equations That Omit Some Spectator Ions Until this point, most of the equations we have encountered have contained either • formulas for neutral compounds, or • separated ions, with a total charge of zero on both sides of the equation. In reactions that involve ions, equations may also be written that omit some but not all of the spectator ions. This can result in an equation that is balanced, but has a net charge on both sides. For example, the reaction of silver nitrate and magnesium chloride solutions can be represented with ionic solid and molecular formulas as 2 AgNO3(aq) + MgCl2(aq) (1) Æ 2 AgCl(s) + Mg(NO3)2(aq) However, separated-ion formulas better represent soluble substances dissolved in water. The total ionic equation is 2 Ag+ + 2 NO3─ + Mg2+ + 2 Cl─ Æ 2 AgCl(s) + Mg2+ + 2 NO3─ (2) A third way to write the reaction is to leave out some of the spectators. For example, the above reaction can be written as 2 AgNO3 + 2 Cl─ Æ 2 AgCl(s) + 2 NO3─ (3) In this equation, the spectator magnesium ions have been left out. The reaction might be written in this format to emphasize that silver nitrate solution will form a precipitate when mixed with any solution that contains chloride ions. Note that this partial ionic equation (3), unlike the total ionic equation, does not have a zero charge on both sides. However, it does have a balanced charge on both sides: the total charge on both sides is positive two. This is an important rule: Equations are considered balanced if they have the same number and kind of atoms and the same net charge on both sides. ©2008 ChemReview.net v. f9 Page 271 Module 13 — Ionic Equations and Precipitates In balancing equations, if the atoms are balanced, and the total charge is the same on both sides, the equation is considered balanced even if some of the atoms and charges that must be present have been left out. In a balanced equation, the total charge on both sides does not need to be zero, but it must be the same on both sides. By definition, in total and net ionic equations, the charges must add up to zero on both sides, but in the partial ionic equations that are also frequently written, the atom counts and total charge must simply be the same on both sides. Leaving Out the Spectators Leaving out the spectators, in both net and in partial ionic equations, provides and equation that is quicker to write than the total ionic equation. The equation focuses on the important particles: those that change in the reaction. In a similar shortcut, in chemistry labs a container may be labeled “Ag+” or “ OH─.” However, if any container is labeled as containing a single ion, it does not mean that only one kind of ion is present. The spectator ions are present, but they have been left out. All stable matter must be composed of balanced positive and negative charges. “Leaving out the spectators” on container labels and in equations is simply a shortcut used to emphasize the ions that react. Practice C: Balance these partial ionic equations. Check answers as you go. Do every other letter, and more if you need more practice. 1. Co(NO3)2 2. AgNO3 + 3. CO32─ + 4. HCO3─ + 5. Al3+ + OH─ Æ + CrO42─ Æ HCl Æ OH─ NO + NO3─ Co(OH)2(s) + NO3─ Ag2CrO4(s) + H2CO3 + Æ H2O Æ H2O + Al + Cl― CO32― NO3 ─ + H+ ANSWERS Practice A: Assume (aq) if no state is shown. 1a. Pb2+(aq) + 2 NO3― (aq) + Cu2+(aq) + 2 Cl―(aq) Æ Cu2+(aq) + 2 NO3―(aq) + PbCl2(s) Net ionic equation: Pb2+(aq) + 2 Cl―(aq) Æ PbCl2(s) 1b.. 6 Na+ + 2 PO43―+ 3 Mg2+ + 3 SO42― Æ Net ionic equation: ©2008 ChemReview.net v. f9 Mg3(PO4)2(s) + 6 Na+ + 3 SO42― 3 Mg2+(aq) + 2 PO43―(aq) Æ Mg3(PO4)2(s) Page 272 Module 13 — Ionic Equations and Precipitates 2a. 1 Fe(NO3)3(aq) + 3 NaOH(aq) Æ 1 Fe(OH)3(s) + 3 NaNO3(aq) 2b. 3 Ca(NO3)2 + 2 K3PO4 Æ 6 KNO3 + 1 Ca3(PO4)2(s) 1 Fe3+ + 3 NO3― + 3 Na+ + 3 OH― Æ 1 Fe(OH)3(s) + 3 Na+ + 3 NO3― 3 Ca2+ + 6 NO3― + 6 K+ + 2 PO43― Æ 6 K+ + 6 NO3― + 1 Ca3(PO4)2(s) Net ionic equation: 1 Fe3+(aq) + 3 OH―(aq) Æ 1 Fe(OH)3(s) Net ionic equation: 3 Ca2+(aq) + 2 PO43―(aq) Æ 1 Ca3(PO4)2(s) 3a. 3b. 4a. 4b. Practice B: Assume (aq) if no state is shown. 1. 2 K+ + 1 SO42― + 1 Sr2+ + 2 NO3― Æ 1 SrSO4(s) + 2 K+ + 2 NO3― 2. 3 Fe2+ + 6 Br ― + 6 Na+ + 2 PO43― Æ 6 Na+ + 6 Br― + Fe3(PO4)2(s) Practice C: (coefficients of 1 may be omitted). 2 OH─ Æ 1 Co(OH)2(s) + 2 NO3─ 2 AgNO3 + 1 CrO42─ Æ 1 Ag2CrO4(s) + 2 NO3─ 3. 1 CO32─ + 2 HCl 4. 1 HCO3─ + 1 OH─ Æ 1. 1 Co(NO3)2 + 2. Æ 1 H2CO3 + 1 Al3+ + 1 NO + 2 H2O Æ * * * * * 5. 2 Cl― 1 CO32― ─ 1 Al + 1 NO3 + 4 H+ 1 H2O + Lesson 13C: Predicting Precipitation Prerequisites: Lessons 7C, 10B, 13A, and 13B. Timing: Do this lesson when you are asked to predict whether a precipitate will form, or to write a formula for a precipitate which forms, when ions are mixed. * * * * * Steps in Predicting Precipitation This key rule for predicting precipitation must be memorized. When two solutions of soluble ions are mixed, • if a new combination is possible that is insoluble, it will precipitate. • If a new possible combination is soluble, its ions will remain separated and dissolved in the solution. To predict whether the mixing of soluble ions will produce a precipitate, you must analyze the solubility of the new ionic combinations that can be formed. Let’s walk through that prediction process one step at a time. Answer these questions in your problem notebook. ©2008 ChemReview.net v. f9 Page 273 Module 13 — Ionic Equations and Precipitates Q. Two separate aqueous solutions are prepared, one by dissolving Ca(NO3)2 and the other by dissolving Na2CO3. a. Write balanced equations showing the ions formed when each of these two ionic solids dissolves in water, then check your answer below. * * * * * a. Ca(NO3)2(s) Æ Ca2+(aq) + 2 NO3―(aq) Na2CO3(s) Æ 2 Na+(aq) + CO32―(aq) * * * * * b. When the two solutions above are mixed, two new combinations of positive and negative ions are possible. Each positive ion can attract either its original negative partner or the new negative ion with which it has been mixed. Fill in the blanks below to show the new possible ion combinations, then add coefficients to balance each new combination for charge. 1 Ca2+ + ____ _______ Æ ___ _____ + ____ NO3― Æ In solution reactions, if no state is shown, assume (aq). * * * * * b. 1 Ca2+ + 1 CO32― Æ 1 Na+ + 1 NO3― Æ * * * * * c. After the arrows, write solid formulas for these new combinations. d. Based on ion solubility rules, label each of the solids as soluble or insoluble. e. Apply the rule: When two solutions of soluble ions are mixed, • if a new combination is possible that is insoluble, it will precipitate. • If the new combination is soluble, its ions remain separated. Will there be a precipitate in this case? If so, what is its solid formula? Write answers for the above three steps, and then check your answers below. * * * * * c. 1 Ca2+ + 1 CO32―Æ CaCO3 1 Na+ + 1 NO3― Å NaNO3 Insoluble by Rule 2. Will precipitate. Soluble by Rule 1. Ions stay separated. e. The precipitate is solid CaCO3 . * * * * * ©2008 ChemReview.net v. f9 Page 274 Module 13 — Ionic Equations and Precipitates f. To write the total ionic equation, write the 4 original reactant ions. Then, for products, write the formula for the solid precipitate, plus the separated ions for the new combination that did not precipitate. Fill in the blanks to give the total ionic equation for the reaction above. 1 Ca2+ +___ ________ +___ ______ + 1 CO32― Æ ___ _______(s) + ___ ______ + ___ ______ g. In your total ionic equation, cross out the spectator ions that are the same on both sides. These ions did not react. Rewrite the equation without the spectators. This is the net ionic equation. * * * * * f. Ca2+ + 2 NO3― + 2 Na+ + CO32― Æ CaCO3(s) + 2 Na+ + 2 NO3― g. Net ionic equation: Ca2+(aq) + CO32―(aq) Æ CaCO3(s) In net ionic equations, spectator ions are omitted that can cancel in the total ionic equation. Net ionic equations show only the particles that change in the reaction. * * * * * Predicting Precipitation – The Chart Method The chart method below can help in predicting whether a precipitate will form. Copy the following chart into your notebook. Solid Formulas Dissolved Ions before mixing Mixed – Possible new ion combinations Possible Precipitates 1. 2. Let’s use an example to see how the chart is used. Q2. When solutions of Pb(NO3)2 and KI are mixed, a yellow precipitate forms. Using the steps on the previous page, fill in the chart above and write the formula for the precipitate. If you need a hint, read a part of the answer below and then try again. * * * * * Answer Ionic compounds in solution are often represented using solid formulas, but when soluble ionic solids dissolve, the ions separate. In these two solutions are these ions: Solid Formulas Dissolved Ions before mixing 1. Pb(NO3)2 Æ 2. KI Æ Pb2+ + 2 NO3─ K+ + I─ ©2008 ChemReview.net v. f9 Page 275 Module 13 — Ionic Equations and Precipitates After they are mixed, the ions can “trade partners.” Two new combinations of positive and negative ions are possible. Solid Formulas Dissolved Ions before mixing Pb(NO3)2 Æ Pb2+ + 2 NO3─ KI Æ K+ + I─ Mixed – Possible new ion combinations Pb2+ + I─ K+ + NO3─ These new combinations may or may not form solid precipitates. Add the possible solid formulas. Solid Formulas Dissolved Ions before mixing Pb(NO3)2 Æ Pb2+ + 2 NO3─ KI Æ K+ + I─ Mixed – Possible new ion combinations Possible Precipitates Pb2+ + 2 I─ Æ PbI2 K+ + NO3─ Æ KNO3 Note that the coefficients are not the same before mixing and after. You must adjust the coefficients so that each new ion combination is balanced for atoms and charge. Will a precipitate form? If a new combination is possible that is insoluble, it will precipitate. Label each of the possible precipitates in the chart as soluble or insoluble. * * * * * PbCl2 is insoluble by rule 2 (Pb2+); KNO3 is soluble by rule 1. The result is Solid Formulas Dissolved Ions before mixing Pb(NO3)2 Æ Pb2+ + 2 NO3─ KI Æ K+ + I─ Mixed – Possible new combinations Possible Precipitates Pb2+ + 2 I─ PbI2 (Insoluble, forms ppt.) Æ K+ + NO3─ Å KNO3 (Soluble, ions stay dissolved) * * * * * Q3. For the above reaction, write the total and then the net ionic equation. * * * * * Answer The chart shows the ions before mixing (column 2) and the products after mixing (column 3 or 4). To write the total ionic equation, copy all of the column two ions on a line on your paper, followed by a reaction arrow. To the right of the arrow, write the new products that form, shown in column 3 or column 4. Adjust the coefficients so that both each ion combination and the overall equation are balanced for atoms and charge. * * * * * To make the precipitate, we need 2 I─. That means we must have 2 K+ to start). Pb2+ + 2 NO3─ + 2K+ + 2 I─ Æ PbI2(s) + 2 K+ + 2 NO3─ ©2008 ChemReview.net v. f9 Page 276 Module 13 — Ionic Equations and Precipitates That is the balanced total ionic equation. Now write the net ionic equation. * * * * * Pb2+(aq) + 2 I─(aq) Æ PbI2(s) Practice A: Net ionic equations show the ions that change. Answers are at the end of this lesson. 1. When AgNO3 solution is mixed with Na2CrO4 solution, a blood red precipitate appears. Fill in a chart like the one above for this reaction, and then write the total and net ionic equations. 2. When potassium hydroxide and cobalt nitrate solutions are mixed, an intense blue precipitate forms. Do the chart, then write the total and net ionic equations. The 3-Line Method The chart method can be used for as long as needed to gain confidence that you are arriving at correct answers. At that point, you can try a quicker “3 line method” (draft, total ionic, and net ionic equations) that handles more of the steps in your head. Let’s learn the method with the following example. Q4. Write the total and net ionic equation identifying the white precipitate that forms when solutions of barium chloride and potassium sulfate are mixed. Write then check your answers to the steps below. 1. On one line, write the separated-ion formulas for the ions being mixed. * * * * * { Ba2+ + 2 Cl─ } + { 2 K+ + SO42─ } Æ 2. After the arrow, write the new possible ion combinations. * * * * * { Ba2+ + 2 Cl─ } + { 2 K+ + SO42─ } Æ { Ba2+ + SO42─ } + { K+ + Cl─ } 3. Use solubility rules to label each new combination as soluble or insoluble. 4. If a new combination of ions is possible that is insoluble, it will precipitate. Write the solid formula for any precipitate that would form. * * * * * { Ba2+ + 2 Cl─ } + { 2 K+ + SO42─ } Æ { Ba2+ + SO42─ } + { K+ + Cl─ } INsoluble Soluble BaSO4(s) 5. That’s the rough draft. Copy the draft result without the brackets, adjusting the coefficients as needed, to write the total ionic equation. ©2008 ChemReview.net v. f9 Page 277 Module 13 — Ionic Equations and Precipitates * * * * * Ba2+ + 2 Cl─ + 2 K+ + SO42─ Æ BaSO4(s) + 2 K+ + 2 Cl─ 6. Write the net ionic equation. * * * * * Ba2+(aq) + SO42─(aq) Æ BaSO4(s) * * * * * Flashcards: Add these to your collection. Run each until perfect for 3 days. But remember, you must also memorize a) a detailed solubility scheme and b) a method to predict whether mixed ions will precipitate, and what the precipitate formula will be. One-way cards (with notch) Back Side -- Answers Chemical equations must be balanced for Atoms and charge Net ionic equations leave out Spectator ions When will mixing two soluble ionic compounds produce a precipitate? If a new possible combination is insoluble When will mixing two soluble ionic compounds not result in a precipitate? If both new possible combinations are soluble Two-way cards (without notch): Ion combinations with these positive ions will always be soluble (alkali metals)+ , NH4+ Ion combinations with these negative ions will always be soluble nitrate, acetate, chlorate, perchlorate Practice B 1. For these, write total and net ionic equations. Try using the 3-line method. a. Ferric nitrate and rubidium hydroxide Æ b. MgSO4(aq) and BaCl2(aq) Æ 2. Combining solutions of magnesium chloride and sodium sulfate, a. what will be the names of the two new combinations that are possible? b. Which of the new combinations are soluble in aqueous solutions? c. Which of the new combinations will precipitate? 3. When these solutions are mixed: NiBr2(aq) + K3PO4(aq) a. What are the solid formulas for the two new combinations that are possible? b. Will a precipitate form in the mixture? If so, what is its name and formula? c. Write the total and the net ionic equations for the reaction. ©2008 ChemReview.net v. f9 Page 278 Module 13 — Ionic Equations and Precipitates ANSWERS ( Assume the state is (aq) if not shown.) Practice A Problem 1 Solid Formula 1. AgNO3 Dissolved Ions before mixing Æ Ag+ + NO3─ 2. Na2CrO4 Æ 2 Na+ + CrO42─ Mixed – Possible new combinations Possible Precipitates 2 Ag+ + CrO42─ Æ Ag2CrO4 (Insoluble, ppt.) Na+ + NO3─ Å NaNO3 (Soluble, does not ppt.) Total ionic equation: 2 Ag+ + 2 NO3─ + 2Na+ + CrO42─ Æ Ag2CrO4(s) + 2 Na+ + 2 NO3─ 2 Ag+(aq) + CrO42─(aq) Æ Ag2CrO4(s) Net ionic equation: Problem 2 Solid Formula Dissolved Ions before mixing Potassium Hydroxide Æ K+ + OH─ Cobalt Nitrate Æ Co2+ + 2 NO3─ Mixed – Possible new combinations Possible Precipitates K+ + NO3─ Å KNO3 (Soluble, does not ppt.) Co2+ + 2 OH─ Æ Co(OH)2 (Insoluble, ppt.) Total ionic equation: 2 K+ + 2 OH─ + Co2+ + 2 NO3─ Æ Co(OH)2(s) + 2 K+ + 2 NO3─ Net ionic equation: Co2+(aq) + 2 OH─(aq) Æ Co(OH)2(s) Practice B 1a. { Fe3+ + 3 NO3─} + { Rb+ + OH─ } Æ { Fe3+ + 3 OH─ } + { Rb+ + NO3─ } Insoluble Soluble Fe(OH)3(s) (That’s the rough draft. To write total and net ionic equations, remove brackets and adjust coefficients so that all atoms and charges balance.) Total ionic: Fe3+ + 3 NO3─ + 3 Rb+ + 3 OH─ Æ Fe(OH)3(s) + 3 Rb+ + 3 NO3─ Net ionic equation: Fe3+(aq) + 3 OH─(aq) Æ Fe(OH)3(s) 1b. { Mg2+ + SO42─ } + { Ba2+ + 2 Cl─} Æ { Mg2+ + 2 Cl─ } Soluble + { Ba2+ + SO42─ } Insoluble BaSO4(s) Total ionic: Mg2+ + SO4─ + Ba2+ + 2 Cl─ Æ Mg2+ + 2 Cl─ + BaSO4(s) ©2008 ChemReview.net v. f9 Page 279 Module 13 — Ionic Equations and Precipitates NET ionic equation: Ba2+(aq) + SO4─(aq) Æ BaSO4(s) 2. a. Magnesium sulfate and sodium chloride. 3. b. Both c. Neither { Ni2+ + 2 Br─ } + { 3 K+ + PO43─} Æ { 3 Ni+2 + 2 PO43─} + { K+ + Br─ } Insoluble Soluble Ni3(PO4)2(s) a. KBr and Ni3(PO4)2 b. Yes. Ni3(PO4)2 (nickel phosphate) c. Total: 3 Ni2+ + 6 Br─ + 6 K+ + 2 PO43─ Æ 1 Ni3(PO4)2(s) + 6 K+ + 6 Br─ Net ionic equation: 3 Ni2+(aq) + 2 PO43─ (aq) Æ Ni3(PO4)2(s) (Note how the coefficients are balanced above. When writing each combination at each stage, adjust coefficients to balance the combination for atoms and charge. Then, for the total ionic equation, adjust the coefficients again to balance each ion combination plus all of the atoms and charges on both sides. If the coefficients do not balance easily, it may indicate an error, and you should double-check your work.) * * * * * Lesson 13D: Precipitation and Gravimetric Calculations Timing: If there is a gap between the time that you are asked to predict which ion combinations precipitate, and when you are assigned calculations involving precipitates, delay this lesson until precipitation calculations are assigned. * * * * * Gravimetric Calculations Stoichiometry answers how much of the reactants are used up and products are formed in chemical reactions. Once the moles of any one reaction component are determined, moles of other components can be solved using simple-whole-number ratios: the coefficients of the balanced equation. In some precipitation calculations, volume and concentration are used to solve for moles. In others, precipitates are dried and weighed to determine moles; a process termed gravimetric because the moles of precipitate are determined by its weight, which is the attraction of its mass by gravity. Precipitation/Gravimetric Stoichiometry Precipitation is a reaction. In most respects, precipitation/gravimetric calculations follow the same rules for reaction stoichiometry that you used in Lessons 12C, but in two ways they often differ. 1. In most previous equations to balance, you were supplied with the formulas of the reactants and products. In precipitation calculations, you will often be asked to both predict all of the product formulas and identify products that precipitate. ©2008 ChemReview.net v. f9 Page 280 Module 13 — Ionic Equations and Precipitates 2. Precipitation calculations can involve measurements for both a solid formula and the ions formed when the solid dissolves in water. To handle these differences for precipitation reactions, we will add these special steps to our stoichiometry process. In precipitation calculations, do stoichiometry steps 3 and 4 as follows. 3. Balance the equation. a. Write and balance a precipitation equation in three parts: Reactants in solid formulas Æ Reactants as separated ions Æ Products b. As you write the product formulas, decide whether a new combination will be soluble and separated, or insoluble and precipitate. Use one of the methods for predicting product formulas and precipitates in Lesson 13C. In the products, write solid formulas for insoluble precipitates and separatedions for combinations that are soluble. c. Once the precipitate formula is identified, in the WANTED and/or DATA, replace ppt. with the formula for the precipitate. If this results in grams of a formula in WANTED or DATA, add the molar mass of the ppt. to the DATA. 4: Write the mol-mol bridge. In the mol-mol bridge, include all chemical formulas that are written after units in the WANTED and DATA. This may result in three or more terms with coefficients, moles, and chemical formulas that are equal, instead of two. Cover the answer below, then apply the steps to the following problem. If you get stuck, read part of the answer below, then try again. Q. If 14.0 mL of Pb(NO3)2 solution is reacted with excess MgCl2 solution, and the resulting precipitate when dried weighs 0.314 grams, what was the original [Pb2+]? * * * * * Answer 1. WANT: = ? mol Pb2+ L Pb2+ soln. (a ratio unit is WANTED) Concentration is a ratio that is constant in a well-mixed solution. The ratio for any sample will be the same as the ratio for the whole solution. We can easily measure the liters in a sample, but we cannot count the moles of ions in a sample directly. However, if we precipitate the ions, weigh the precipitate, and identify the precipitate formula, we can find the moles of ions in the original sample. We can then divide to find the mol/L ratio for the sample, and that is the WANTED unit. Since weighing the dried precipitate is one step, this is a gravimetric calculation. ©2008 ChemReview.net v. f9 Page 281 Module 13 — Ionic Equations and Precipitates 2. DATA: 14.0 mL Pb(NO3)2 soln. = 0.314 g ppt. (Equivalent: 2SUA-R) In the calculation of a WANTED ratio based on a reaction, two DATA amounts will be equivalent in the reaction (Lesson 12C). The MgCl2 is in excess. Amounts of reactants in excess can be ignored in the DATA, since they do not determine the amounts of reactants used up or products formed (Lesson 10F). 3. Balance. Since this is a precipitation reaction, apply the special steps above. a. Write the balanced equation for precipitation in 3 parts: Reactants as solid formulas, reactants in separated-ions, and products as either precipitates or as separated, soluble spectator ions, depending on their state in the products. Solid Reactants: 1 Pb(NO3)2 + 1 MgCl2 Æ Separated Reactants: Æ 1 Pb2+ + 2 NO3─ + 1 Mg2+ + 2 Cl─ Æ Products: Æ 1 PbCl2(s) + 1 Mg2+ + 2 NO3─ Adjust coefficients so that all three parts balance for atoms and charge. b. Decide the precipitate formula. Upon mixing the two solutions, two new ion combinations can form. • • • One new combination is lead ion with chloride ion. By the solubility rules in Lesson 13A, the combination of Pb2+and Cl─ is insoluble. A possible new combination that is insoluble will precipitate, so PbCl2 will precipitate. The other new possible combination is Mg2+and NO3─ ions. All combinations that include nitrate ion are soluble. Write these ions as separated on the products side. The only precipitate is therefore PbCl2. The ions that do not precipitate are written as separated ions in the products. c. In the DATA, replace ppt. with its solid formula: DATA: 14.0 mL Pb(NO3)2 soln. = 0.314 g ppt. PbCl2(s) (Equivalent) Now that the DATA includes grams of a formula, what can be added to the DATA that will likely be needed to solve? * * * * * 278.1 g PbCl2 = 1 mol PbCl2 (grams prompt) 4. Bridge conversion. In precipitation reactions, write mole ratios between all of the chemical formulas which are written after units in the WANTED or DATA. In this problem, the WANTED and DATA involve measurements of three chemical formulas: Pb2+, Pb(NO3)2, and PbCl2. Write the bridge ratios for those three formulas using the coefficients in the balanced equations above. * * * * * ©2008 ChemReview.net v. f9 Page 282 Module 13 — Ionic Equations and Precipitates Bridge: 1 mol Pb2+(aq) = 1 mol Pb(NO3)2(aq) = 1 mol PbCl2(s) Any two of those three terms can be used as a bridge conversion. * * * * * 5. SOLVE. For reaction calculations in which the answer unit is a ratio, our strategy is to find a value for the top and bottom WANTED units separately, then divide (see Lesson 12C). The steps are a. Label the DATA equality that has two amounts that are equivalent at the endpoint as “Equivalent” or “2SUA-R.” b. Solve for the WANTED top or bottom unit that is not moles first, using as a given the side of the equivalency that measures the WANTED formula or sample. c. Solve for moles WANTED using single-unit stoichiometry. Start with the other half of the equivalency as the given. c. Divide the two WANTED amounts to find the WANTED ratio. * * * * * The WANTED unit that is not moles is L Pb2+. Pick one of the terms in the equivalency to convert to Pb2+. Which one? In stoichiometry, pick the term in the equivalency that measures the WANTED substance or sample. Neither of the two equivalent amounts has the formula Pb2+. However, the labels Pb(NO3)2 and Pb2+ are simply two ways to identify the same solution: one label has the nitrate spectator ions included, and the other does not. The mL volume of Pb(NO3)2 is in the equivalency, so use that term as your given. ? L Pb2+ soln. = 14.0 mL Pb(NO3)2 soln. = 0.0140 L Pb(NO3)2 = 0.0140 L Pb2+ soln. An good general rule is: If you get stuck, add more complete labels to the WANTED and DATA. In this case, by labeling all of the volume units as soln., it is a indication that they can be related. Now solve for the other WANTED unit and then check below. * * * * * Starting from the other half of the equivalency as given, ? mol Pb2+ = 0.314 g PbCl2 ● 1 mol PbCl2 ● 1 mol Pb2+ = 1.129 x 10─3 mol Pb2+ 278.1 g PbCl2 1 mol PbCl2 Finish the problem, and then check below. * * * * * The sample of Pb2+ solution was found to have 1.129 x 10─3 mol Pb2+ in 0.0140 L Pb2+ soln. Knowing those amounts, we can find the WANTED ratio. ©2008 ChemReview.net v. f9 Page 283 Module 13 — Ionic Equations and Precipitates ─3 2+ ? mol Pb2+ = 1.129 x 10 mol Pb = 2+ 2+ L Pb soln. 0.0140 L Pb soln. 0.0806 mol Pb2+ L Pb2+ soln. * * * * * Flashcards: Add these to your collection. Run each until perfect for 3 days, then move them to stack 2 (see Lesson 6E). One-way cards (with notch) Back Side -- Answers In gravimetric or precipitation calculations, what special rule applies to the balance step? Write solid reactants Æ separated reactants Æ products In gravimetric or precipitation calculations, when you identify the ppt. formula… If grams ppt is in WANTED or DATA, add the molar mass to the DATA Practice: Memorize the special rules for precipitate stoichiometry, then apply them to these problems. If you get stuck, read a part of the answer and try again. 1. A 25.0 mL sample of K2SO4 solution is reacted with an excess amount of BaCl2 solution. Assuming that all of the sulfate ions precipitate, if the mass of the dried precipitate is 1.167 grams, what was the original [K2SO4]? 2. 50.0 mL of a solution containing Pb2+ requires 12.0 mL of a 0.200 M NaCl solution to precipitate all of the lead ions. What was the original [Pb2+]? ANSWERS 1. 1. WANTED: 2. DATA: ? mol K2SO4 L K2SO4 soln. 25.0 mL K2SO4 soln. = 1.167 g ppt. (Equivalent – 2SUA-R) (The problem is about a chemical reaction. The WANTED and DATA involve 2 substance (the ppt. being one.) That’s the stoichiometry prompt. All stoichiometry begins with the same 4 steps.) 3. Balance. a. (In precipitation, balance in 3 parts) Solid Reactants: Separated Reactants: Products: 1 K2SO4(aq) + 1 BaCl2(aq) Æ Æ 2 K+(aq) + 1 SO42─(aq) + 1 Ba2+(aq) + 2 Cl─(aq) Æ Æ 1 BaSO4(s) + 2 K+(aq) + 2 Cl─ (aq) b. (Identify the precipitate. Since KCl is soluble, the ppt. must be BaSO4. c. Adjust the DATA.) DATA: 25.0 mL K2SO4 soln. = 1.167 g ppt. BaSO4(s) (equivalent – 2SUA-R) (What additional key information can now be added to the DATA? * * * * * ©2008 ChemReview.net v. f9 Page 284 Module 13 — Ionic Equations and Precipitates 233.4 g BaSO4 = 1 mol BaSO4 4. Bridge. (grams of a formula = g prompt) 1 mole K2SO4 = 1 mole BaSO4 (K2SO4 and BaSO4 are the only formulas that are written after units in the WANTED or DATA. (If needed, adjust your work and finish from here.) * * * * * 5. SOLVE. (Since the answer unit is a ratio, find amounts for the two WANTED units separately. a. Label the equivalency in the DATA. b. First find the WANTED unit that is not moles, choosing as a given the side of the equivalency that measures the formula WANTED.) ? L K2SO4 = 25.0 mL K2SO4 = 0.0250 L K2SO4 c. (Find moles WANTED using the other half of the equivalency as a given.) * * * * * ? mol K2SO4 = 1.167 g BaSO4 ● 1 mol BaSO4 ● 1 mol K2SO4 = 5.000 x 10─3 mol K2SO4 233.4 g BaSO4 1 mol BaSO4 d. (Find the final WANTED unit.) * * * * * ─3 ? mol K2SO4 = 5.000 x 10 mol K2SO4 L K2SO4 0.0250 L K2SO4 solution 2. 1. WANT: 2. DATA: = 0.200 mol K2SO4 L K2SO4 ? mol Pb2+ = L Pb2+ soln. 50.0 mL Pb2+ soln = 12.0 mL NaCl soln. 0.200 mol NaCl = 1 L NaCl soln. (equivalent – 2SUA-R) (M prompt – a ratio) 3. Balance. a. (Write the balanced equation for precipitate formation in three parts: solid, separated, products.) 1 Pb2+ + 2 NaCl Æ 1 Pb2+ + 2 Na+ + 2 Cl─ Æ 1 PbCl2(s) + 2 Na+ (The anion that was initially combined with lead ion is not known, but it is not needed as long as the above equations are balanced for atoms and charge. b. Identify: The precipitate must be PbCl2. c. Adjust: Since the ppt. amount is not measured in the DATA, there is no DATA to adjust.) 4. Bridge. (The WANTED and DATA include measurements (units and formulas) for only 2 substance formulas: Pb2+ and NaCl.) Bridge: 1 mol Pb2+ = 2 mol NaCl (If needed, adjust your work and solve from here.) * * * * * ©2008 ChemReview.net v. f9 Page 285 Module 13 — Ionic Equations and Precipitates 5. SOLVE. (Since the answer unit is a ratio, find amounts for the two WANTED units separately. a. Label the equivalency in the DATA. b. First find the WANTED unit not moles, choosing as a given the side of the equivalency that measures the formula WANTED.) ? L Pb2+ soln. = 50.0 mL Pb2+ = 5.000 x 10─2 L Pb2+ (mL to L, divide by 1,000) c. (Using other half of equivalency as given, find moles WANTED using stoichiometry steps.) ? mol Pb2+ = 12.0 mL NaCl ● 1 L ● 0.200 mol NaCl ● 1 mol Pb2+ = 1.200 x 10─3 103 mL 1 L NaCl 2 mol NaCl mol Pb2+ d. (Find the final WANTED unit. Above, in the sample of the WANTED solution, you found 1.20 x 10─3 mol Pb2+ was in 0.050 L Pb2+.) ? mol Pb2+ L Pb2+ = 1.200 x 10─3 mole Pb2+ 5.000 x 10─2 L Pb2+ = 0.0240 M Pb2+ * * * * * Summary: Solubility and Precipitation 1. Most ionic solids can be characterized as soluble or insoluble in water. The rules for solubility must be memorized, and exceptions occur. Some frequently used rules are a. compounds containing alkali-metal atoms, and NH4+, NO3─ , CH3COO─, ClO3─ , and ClO4─ ions are nearly always soluble in water; b. except in the above cases, compounds containing Pb2+ , Hg22+, Ag+, CO32─, PO43─ , S2─, or CrO42─ ions will generally be insoluble in water. 2. When two solutions of soluble ions are mixed, • if a new combination is possible that is insoluble, it will precipitate; • if a new combination is soluble, its ions will remain separated. 3. Total ionic equations show all of the ions and precipitates present when two soluble solutions are mixed. Net ionic equations include the ions and solids that change in a reaction, and omit spectator ions that do not change. 4. In precipitation calculations: a. Write a balanced equation for precipitate formation in 3 parts. Reactants as solid formulas Æ Reactants as separated ions Æ Products b. Use solubility rules to determine which ions precipitate. c. Use stoichiometry steps to solve. 5. In general, to understand the reactions of ionic compounds, • Re-write the reactants in their separated-ions format; • Look for reactions among the new possible ion combinations. # # # # ©2008 ChemReview.net v. f9 Page 286 Module 14 — Acid-Base Neutralization Module 14 — Acid-Base Neutralization Timing: This module covers acid-base neutralization. Other acid-base topics, including pH, weak acids and bases and buffers are covered in Modules 27 - 29. There are two types of acid-base neutralization calculations that may be assigned in your course. • If all of the neutralization calculations that you are assigned supply chemical formulas for the products in the reactions, you do not need to do Module 14. This type of calculation was covered in Lesson 12C. • If your course assigns in which you must predict the product formulas for acid-base neutralization, complete Module 14. * * * * * Lesson 14A: Ions In Acid-Base Neutralization Prerequisites: Lessons 7B and 7C. Pretest: If you can do all of the following problems, you may skip Lessons 14A and 14B. Check answers at the end of this lesson. Assuming complete neutralization of all protons and basic ions, write product formulas and balance these. a. KHC2O4 + KOH Æ b. H3Unk + Mg(OH)2 Æ c. HCO3─ + OH─ Æ * * * * * Terminology Many substances can be classified as acids or bases (and some can be both). There are a variety of definitions for acids and bases, with each definition helpful in certain kinds of reactions. In an acid-base neutralization reaction, an acid and a base are the reactants. When they are mixed together, they react, and both are used up. Both the acid and the base are said to be neutralized. For the limited purpose of studying neutralization, we will define • an acid as a substance that creates H+ ions when dissolved in water, and • a base as a substance that can react with (use up) H+ ions. Because strong acids and bases can react with many substances, they are often termed corrosive: they may damage a surface, metal, or fabric. When an acid or base is neutralized, its most reactive ions are used up, and its corrosive power is reduced. ©2008 ChemReview.net v. f9 Page 287 Module 14 — Acid-Base Neutralization Understanding Neutralization As substances, acids and bases may be ionic or covalent compounds. However, when dissolved in water, however, acids and bases react with the water to form ions. A key to understanding neutralization is to write the acid and base reactants as separated ions. Acids When they are dissolved in water, acids form H+ ions plus other ions. The ions formed will always be present in ratios that guarantee electrical neutrality. A strong acid is one that separates essentially 100% into ions when it dissolves in water. Example – Nitric acid: 1 HNO3 H2O Æ Other frequently encountered strong acids include 1 H+ + 1 NO3─ (goes ~100%) • HCl , hydrochloric acid, ionizes in water to form an H+ ion and a chloride ion (Cl─). • H2SO4 , sulfuric acid, is used in many car batteries. It is termed a diprotic acid because each neutral H2SO4 molecule can release two H+ ions. Strong acids can neutralize both strong and weak bases. Weak acids ionize only slightly in water. An example is CH3COOH (acetic acid), the active ingredient in vinegar. Acetic acid ionizes slightly in water to form one H+ ion and one acetate anion (CH3COO─). The four italicized acid names above are encountered frequently. Their names and formulas should be memorized. Bases Strong bases can neutralize both strong and weak acids. Strong bases often contain hydroxide ions. Examples include • NaOH (sodium hydroxide); • KOH (potassium hydroxide); and • Ca(OH)2 (calcium hydroxide), which ionizes to form two hydroxide ions. Compounds that contain carbonate ions (CO32─) are also bases. Carbonates are weaker bases than hydroxides, but carbonate ions are strong enough as bases to neutralize both strong and moderately weak acids. Examples of carbonates include • Na2CO3 (sodium carbonate) and • CaCO3 (calcium carbonate). Hydrogen carbonate ions (HCO3─, also called bicarbonate ion) can also react as a base, but the HCO3─ ion is a weaker base than carbonate and hydroxide ions, and it reacts only with only acids that are relatively strong. Many other molecules and ions can act as bases, but those containing OH─, CO32─, or HCO3─ ions are the bases most frequently used in acid-base neutralization. ©2008 ChemReview.net v. f9 Page 288 Module 14 — Acid-Base Neutralization Electrolytes Because acids and bases form ions when they dissolve in water, they are termed electrolytes: their solutions can conduct electricity. Compounds that ionize close to 100% are called strong electrolytes. Strong acids and strong bases are strong electrolytes. The Structure of H+: A Proton Neutral hydrogen atoms contain one proton and one electron. (About 1% of H atoms also contain one or two neutrons, but the neutrons have no impact on the types of reactions in which hydrogen participates.) An H+ ion is a hydrogen atom without an electron, so H+ ions behave chemically as a single proton. The terms H+ ion and proton are often used interchangeably to describe the active particle in an acid. Memorize: acid ion = H+ = proton. Identifying Acids and Bases From a chemical formula, how can you tell whether a substance will be an acid or a base? y Compounds that ionize in water to form H+ ions are acids. y Compounds that contain OH─, CO32─, or HCO3─ ions can act as bases. To predict whether a particle formula will be an acid or a base, write the equation for the formula separating into ions. Most of the ions should be familiar, and the equation must be balanced for atoms and charge. Practice A: For the reaction in which the compounds below ionize in water, write balanced equations showing the ions formed, then label each initial reactant as an acid or a base. Answers are at the end of the lesson. For help, review Lesson 7C. a. LiOH H2O b. HBrO4 Æ Æ c. HCN Æ d. Na2CO3 Æ e. Ca(OH)2 Æ f. NH4OH Æ Identifying Acidic and Non-Acidic Hydrogens Hydrogen atoms in compounds can be divided into two types. • Acidic hydrogens are generally defined as those that react with hydroxide ions, and • non-acidic hydrogens are those that do not. ©2008 ChemReview.net v. f9 Page 289 Module 14 — Acid-Base Neutralization Compounds often contain both acidic and non-acidic hydrogens. For example, in CH3COOH (acetic acid), the H atom at the end of the formula reacts with NaOH, but the other three H atoms do not. The H at the end is the acidic hydrogen. The other H atoms are not acidic hydrogens. In a substance formula, how can you predict which hydrogens in a compound will be acidic, and which will not? In general, the rules are: • If one or more H atoms is written toward the front of a formula, while others are not, the H atoms at the front will be acidic, the others will not. Example: Acetic acid is often written as HC2H3O2. Only the H in front is acidic. • The H at the end of a ─COOH (also written ─CO2H) functional group is acidic. Examples: In C6H5COOH, only the H at the end is acidic. In C3H7CO2H, only the H at the end is acidic. • If H is the second atom in the formula, written after a metal atom and before other atoms, it is acidic. Examples: In KHC8H4O4, the first H (and only the first) is acidic. In NaH2PO4, the two H’s after the metal are acidic. • If a substance with only one H reacts with hydroxide ion, the H is acidic. Practice B 1. Draw an arrow toward and count the acidic hydrogens in these compounds. a. NaH2PO4 d. H3AsO4 b. C6H5COOH e. KHC8H4O4 c. H2C4H4O6 f. NaHSO4 2. Fill in the blanks to show the number of protons formed when these compounds ionize in water. a. C3H7CO2H Æ ___ H+ b. HC2H3O2 Æ ___ H+ c. NaH2(C3H5O(COO)3) Æ ___ H+ ©2008 ChemReview.net v. f9 Page 290 Module 14 — Acid-Base Neutralization ANSWERS Pretest: Coefficients of 1 may be omitted as understood. a. 1 KHC2O4 + 1 KOH Æ 1 H2O + 1 K2C2O4 b. 2 H3Unk + 3 Mg(OH)2 Æ 6 H2O + 1 Mg3(Unk)2 c. HCO3─ + OH─ Æ H2O + CO32─ Practice A a. LiOH Æ Li + + OH─ Base b. HBrO4 Æ H+ + BrO4─ Acid c. HCN Æ H+ + CN─ d. Na2CO3 Æ 2 Na+ + CO32─ Base Acid e. Ca(OH)2 Æ Ca2+ + 2 OH─ f. NH4OH Æ NH4+ + OH─ Base Base Practice B 1. a. NaH2PO4 Two d. H3AsO4 2 b. C6H5COOH Three e. KHC8H4O4 a. C3H7CO2H Æ 1 H+ One One c. H2C4H4O6 Two One f. NaHSO4 b. HC2H3O2 Æ 1 H+ c. NaH2(C3H5O(COO)3) Æ 2 H+ * * * * * Lesson 14B: Balancing Hydroxide Neutralization Prerequisites: Lesson 14A. * * * * * Hydroxide Neutralization In the reaction of an acid and a hydroxide, the neutralization reaction forms water (which can be written as H─OH or HOH or H2O). H+ + OH─ Æ H-OH(l) The reaction of an acid and a hydroxide is driven to completion by the formation of water: a low potential energy molecule. Whenever a physical or chemical system can go to lower potential energy, there is a strong tendency to do so. The reaction of acids with compounds containing hydroxide ions can be represented by the general equation An acid + a base containing OH─ Æ H2O + a salt (1) A typical acid-hydroxide neutralization is the reaction of hydrochloric acid with sodium hydroxide to form sodium chloride (also known as table salt). HCl(aq) + NaOH(aq) ©2008 ChemReview.net v. f9 Æ H-OH(l) + NaCl(aq) (2) Page 291 Module 14 — Acid-Base Neutralization The state (aq) means aqueous (dissolved in water). Most (but not all) acid-base reactions are carried out in water. In the acid-base reaction equations in these lessons, you may assume that the water is liquid and the formulas for other compounds and ions are aqueous (aq) unless otherwise noted. Writing water in the form H─OH form helps to emphasize the reaction that occurs between acids and hydroxide ions. Equation (2) above is one way that this reaction is represented. However, both HCl and NaOH, when dissolved in water, separate completely into ions. The table salt in the solution after the reaction also exists as separate ions of Na+ and Cl─. Re-writing the equation to show the separated ions that actually exist in the solution, the reaction is H+ + Cl─ + Na+ + OH─ Æ H─OH(l) + Na+ + Cl─ (3) Note in reaction (3) that the sodium and chloride ions are spectators: they do not change during the reaction. The term salt in reaction (2) refers to the combination of spectator ions that are the products, in addition to water, when the acid and hydroxide ion react. Balancing Neutralization If formulas are supplied for all the reactants and products, neutralization equations can be balanced by trial and error using the methods in Lesson 10B. However, in acid-base neutralization problems, often the product formulas are not supplied. In these problems, you may be asked to • predict formulas for all of the products of the reaction, or • add the coefficients for the acid and base without knowing the products. The following rules will solve these problems. Predicting All Products of Hydroxide Neutralization In neutralization, by separating the solid (molecular) reactant formulas into ions, you can predict the products and balancing the equation. In hydroxide neutralization, the key rule is If an acid reacts with OH─, one of the products is H─OH. Knowing H─OH is one product, you can often predict the other product formula(s). Complete the steps below in your notebook. Q. Write a balanced equation for the complete neutralization of H3PO4 (phosphoric acid) by Ca(OH)2 (calcium hydroxide). Steps: 1. Write the acid and base reactants in their solid (molecular) formulas. 2. On the line below, re-write each reactant inside parentheses ( ) in its separated-ion format. 3. After the reactants, add “ Æ H─OH + ______ + ______”. * * * * * ©2008 ChemReview.net v. f9 Page 292 Module 14 — Acid-Base Neutralization Solid: H3PO4 + Ca(OH)2 Æ Separated: ( 3 H+ + PO43─ ) + ( Ca2+ + 2 OH─ ) Æ H-OH + ______ + ______ 4. Add lowest-whole-number coefficients in front of the parentheses ( ) to balance the H+, OH─, and H-OH. * * * * * Separated: 2 ( 3 H+ + PO43─ ) + 3 ( Ca2+ + 2 OH─ ) Æ 6 H-OH + ____ + ____ ^ ^ ^ [ ( 6 H+ ) ( 6 OH─ ) Æ ( 6 H-OH ) ] The total H+ ions must equal the total OH─ ions must equal the total H2O. 5. Add in the products side blanks the formulas and coefficient totals for the ions on the left that are not H+and OH─. 6. Move the left side coefficients that are in front of the ( ), plus the coefficient of the water, up to the top line. 7. Finish adding coefficients to the top equation. To write a molecular formula for the remaining product, use the rules for writing ionic solid formulas in Lesson 7C. * * * * * Solid: 2 H3PO4 + 3 Ca(OH)2 Æ 6 H2O + 1 Ca3(PO4)2(s) Separated: 2 ( 3 H+ + PO43─ ) + 3 ( Ca2+ + 2 OH─ ) Æ 6 H2O + 2 PO43─ + 3 Ca2+ In most neutralization reactions, the ions that are not H+ and OH─ will simply remain as aqueous “spectator ions,” dissolved in the final solution. In this problem, however, calcium and phosphate ions are an insoluble combination. If a combination can form that is insoluble, it will precipitate. In this reaction, we have both a neutralization and a precipitation. 8. Check that the final equation is balanced. Practice A. Balance by inspection or the methods above. Assume that the acids and bases are completely neutralized. Do every other part, and more if you need more practice. 1. Write the product formulas in the solid (molecular) format and balance the equation. a. HNO3 + KOH Æ b. KOH + H2SO4 c. H2SO4 + Al(OH)3 Æ Æ 2. Write reactant and product formulas, then balance the equation. Write final formulas in the ionic-solid (molecular) format. a. Barium hydroxide plus sulfuric acid b. Hydrochloric acid plus magnesium hydroxide ©2008 ChemReview.net v. f9 Page 293 Module 14 — Acid-Base Neutralization Balancing Neutralization with Spectators Omitted In all stable substances and mixtures, the total of all of the positive and negative charges must add up to zero. However, as a shortcut, spectator ions are often omitted when representing substances or writing reaction equations. In such cases, the written charges may not add up to zero. For example, in the lab, solutions of acids and bases may be labeled as simply H+ or OH─ to emphasize the reactive particles. In those solutions, however, there must also be other ions that balance the overall charge. Similarly, in writing neutralization equations, partial ionic equations may be written that leave out spectators. In these equations, if some or all spectators are omitted, the total charge may not be neutral on both sides, but that is considered as an acceptable shortcut when writing balanced equations. For a written reaction equation to be considered balanced, what is required is that the atoms and the total charge be the same on both sides (but not necessarily zero). To balance a neutralization equation in which some spectators have been left out, use the same steps as above: break the formulas into familiar ions, one reactant including H+ and the other including a basic ion, then balance the atoms and total charge on each side. Try this example. Q. Write the products and balance: HSO4─ + OH─ Æ * * * * * • Inside parentheses, break the reactants into familiar ions. Form water on the right. • Add coefficients that balance the particles that form water. • Balance the particles that don’t react. • Make sure that the atoms balance and the total charge is the same in all three parts. 1 HSO4─ + 1 OH─ Æ 1 ( 1 H+ + 1 SO42─ ) + 1 OH─ Æ 1 H-OH + 1 SO42─ Atoms balance, and in all three parts, the total charge is ─2. Balanced! Practice B. Check answers as you go. Do every other letter, and more for more practice. 1. Write product formulas and balance the equation. Assume all acids and bases are totally neutralized. Products may be molecules or ions. a. H+ + b. HSO4─ + KOH Æ c. KHSO4 + OH─ d. CH3COOH + ©2008 ChemReview.net v. f9 Al(OH)3 Æ Æ OH─ Æ Page 294 Module 14 — Acid-Base Neutralization Partial Balancing To solve most neutralization stoichiometry, we will need only the coefficients for the reactants: the acid and the base. This partial balancing can be completed if know the formula for one product, and in acid-hydroxide neutralization, we do. One product is always H-OH. For this problem, write H-OH as a product, balance the left side, and then check below. Q. What is the ratio of reaction for H2SO4 + Al(OH)3 Æ * * * * * Either balance by inspection (total H+ = total OH─) or by using these steps. 1. Below the two reactants, write the number of acidic and basic ions in the reactants. 2. On the right, add one product of the reaction. H2SO4 + ( 2 H+ ) + Al(OH)3 Æ H─OH + … (3 OH─ ) Æ H─OH + … 3. Add the coefficients to balance the atoms and charge. H2SO4 + 3 ( 2 H+ ) + Al(OH)3 Æ 2 (3 OH─ ) H─OH + … Æ 6 H─OH + … 4. Transfer the coefficients to the original reaction equation. 3 H2SO4 + 2 Al(OH)3 Æ 6 H─OH + … 3 ( 2 H+ ) + 2 (3 OH─ ) Æ 6 H─OH + … The reactant ratios will be all that is needed to solve most neutralization stoichiometry. Practice C. Assume all reactants are completely neutralized. Balance by inspection or using the steps above. Do every other problem, and more if you need more practice. 1. Balance the coefficients of the two reactants. a. CsOH + H2SO4 b. Ca(OH)2 + nitric acid Æ c. HSO4─ + OH─ Æ Æ 2. Add ratios of reaction for these reactants. a. CH3COOH b. Calcium hydroxide + c. NaHC2O4 + d. Sodium hydroxide + ©2008 ChemReview.net v. f9 + NaOH Æ HC2H3O2 Æ Al(OH)3 Æ KHC8H4O4 Æ Page 295 Module 14 — Acid-Base Neutralization Balancing with an Unknown Formula In some neutralization calculations, the formula for an acid or the base is not supplied, but the number of protons in the acid, or basic ions in the base, is provided. Often this information is all that you need to balance the acid-base ratio. Try this example. Q. A solid acid has an unknown formula but is known to contain three acidic hydrogens. What will be the ratio for the reaction of this acid with NaOH? Check part of the answer below if you need a hint. * * * * * Answer One way to balance is to write the acid formula as H3Unk , where the Unk stands for unknown, and H3 represents three acidic hydrogens. The two reactants can then be written as: H3Unk + NaOH Æ Complete the reactant balancing. * * * * * H3Unk + NaOH Æ 1 ( 3 H+ ) + 3 ( OH─ ) Æ 3 H─OH + …. The acid-base ratio must be 1 H3Unk + 3 NaOH Æ A formula could be written for the other products, but it would be speculation. The acid anion could remain intact, or it could decay in some fashion. However, for most neutralization stoichiometry, formulas for the other products are not required. The acidbase ratio on the left side of the equation will be all that is needed to solve. * * * * * Summary: Neutralization rules so far. 1. Acid-base neutralization is an ionic reaction. To understand ionic reactions, write the separated-ion formulas. 2. Ions: Acids contain H+. The reacting particle in acids = H+ = a proton. Bases include compounds with hydroxide (OH─), carbonate (CO32─), and hydrogen carbonate (HCO3─) ions. 3. Products: For acids + OH─, one product is water: H-OH. H+ + OH─ Æ H-OH 4. Balancing: To predict the products and balance the equations, • Write the separated-ion formulas in ( ). • Write one product. • Finish by balancing atoms and charge. 5. To balance when a formula is unknown, • If a substance has 2 acidic hydrogens, write its formula as H2Unk. • If a base has 3 hydroxides, write Unk(OH)3. ©2008 ChemReview.net v. f9 Page 296 Module 14 — Acid-Base Neutralization Practice D: Learn the rules above, then do these problems. Assume that all reactants are completely neutralized. 1. Supply the ratios of reaction for the two reactants. a. H2Unk + Sr(OH)2 Æ b. H2SO4 + Unk(OH)3 Æ c. HCl + UnkOH Æ 2. Add coefficients to balance the two reactants. a. An unknown acid with two acidic hydrogens is totally neutralized by potassium hydroxide. b. An unknown base with three hydroxide ions is totally neutralized by nitric acid. ANSWERS Practice A Coefficients of one may be omitted. Any coefficient ratios which are the same as these are not incorrect, but lowest whole-number ratios are preferred. 1 1 HNO3 + b. 2 KOH + 1 H2SO4 c. 3 H2SO4 + 2 Al(OH)3 Æ 2. a. b. 1 KOH Æ 1 H2O + 1 KNO3 a. 2 H2O + 1 K2SO4 Æ 1 Ba(OH)2 + 1 H2SO4 Æ 1 Al2(SO4)3 + 6 H2O 2 H2O + 1 BaSO4 2 HCl + Mg(OH)2 Æ 2 H2O + 1 MgCl2 Practice B 1. a. 3 H+ + 1 Al(OH)3 Æ 3 H-OH + Al3+ + 1 KOH Æ 1 H-OH + 1 K+ + 1 SO42─ c. 1 KHSO4 + 1 OH─ Æ 1 H-OH + 1 K+ + 1 SO42─ d. 1 CH3COOH + 1 OH─ Æ 1 H-OH + 1 CH3COO─ b. 1 HSO4─ Practice C To balance the reactants, write one product of the reaction. 1. a. 2 CsOH + 1 H2SO4 Æ 2 H-OH + … b. 1 Ca(OH)2 + 2 HNO3 Æ 2 H-OH + … c. 1 HSO4─ + 1 OH─ ©2008 ChemReview.net v. f9 Æ 1 H-OH + … Page 297 Module 14 — Acid-Base Neutralization 2. a. 1 CH3COOH + 1 NaOH b. 1 Ca(OH)2 + 2 HC2H3O2 Æ 1 H2O + … Æ 2 H2O + … c. 3 NaHC2O4 + 1 Al(OH)3 Æ 3 H2O + … d. 1 NaOH + 1 KHC8H4O4 Æ 1 H2O + … Practice D 1. a. 1 H2Unk + 1 Sr(OH)2 Æ 2 H-OH + … b. 3 H2SO4 + 2 Unk(OH)3 Æ 6 H2O + … c. 1 HCl + 1 UnkOH Æ H-OH + … 2. a. 1 H2Unk + 2 KOH Æ 2 H2O + … b. 3 HNO3 + 1 Unk(OH)3 Æ 3 H2O + … * * * * * Lesson 14C: Acid-Hydroxide Neutralization Calculations Prerequisites: Lessons 7C, 10E, 11D, 12C, 14A+B. * * * * * Terminology Titration is an experimental technique used to gather the information needed for stoichiometry calculations. Calibrated burets are used to precisely measure the amount of solution added as a chemical reaction takes place. Indicators are dyes used in titration that change color at the instant the moles of two reacting particles are equal or have reacted in a simple-whole-number ratio. When this equivalence point is reached, a change in indicator color signals the endpoint of the titration. Acid-base titration is simply neutralization in which the amounts of acid and base are carefully measured. In an acid-base neutralization, an acid and base are mixed. If one of the two reactants is a strong acid or base, the reaction will proceed until the limiting reactant is essentially completely used up. Standard solution stoichiometry methods can then be used to calculate the amounts of reactants used up and products that form. In the special case of a titration of an acid with a base that contain hydroxide ions, when the equivalence point is reached, the moles of H+ ions from the original solution that have reacted equal the moles of OH─ ions in the original base solution that have reacted. At an acid-hydroxide endpoint, moles H+ reacted = moles OH─ reacted ©2008 ChemReview.net v. f9 Page 298 Module 14 — Acid-Base Neutralization When an acid and a hydroxide ion are mixed, one reaction is always 1 H+ + 1 OH─ Æ 1 H-OH(l) When titrating a weak acid or base, the opposite solution must be strong, and a careful selection of the indicator dye will be required to show a sharp endpoint. However, for all acids and bases, whether one or both is strong, stoichiometry calculations are done using the same steps. Neutralization Calculations Based on Partial Balancing To solve stoichiometry, you do not always need a complete balanced equation. What you need is the bridge conversion: a numeric ratio between the WANTED and given substances in the reaction. In most neutralization calculations, the WANTED and given are the acid and the base reactants. Their coefficients can be determined by the partial balancing practiced in Lesson 14B. This special rule is: In neutralization stoichiometry, use partial balancing at Step 3 to write the Step 4 bridge. Once partial balancing supplies the acid and base coefficients, neutralization calculations can be solved using the same stoichiometry steps that were practiced in Lesson 12C. Try this example. Q. If 19.29 mL of a 0.120 M KOH solution is needed to completely neutralize 0.1484 grams of an unknown acid, given that acid has three acidic protons, what is molar mass of the acid? If you get stuck, read a portion of the answer until you are unstuck, then try again. * * * * * Answer: Your paper should look like this. 1. WANT: ? g acid mol acid 2. DATA: 0.1484 g acid = 19.29 mL KOH (write the unit WANTED) (2SUA-R: equivalent at endpt.) 0.120 mol KOH = 1 L KOH 3. Balance. (For acid-base neutralization, use partial balancing) 1 H3Unk + 3 KOH Æ 3 H2O + … 4. Bridge. 1 mol H3Unk = 3 mol KOH Rules used above include • Reaction calculations with data for two substances are solved by stoichiometry. • All stoichiometry starts with the same 4 steps: WDBB. • Solving for a ratio unit, all of the DATA will be in equalities. • In stoichiometry for a ratio unit, two amounts will be equivalent at the endpoint. • In neutralization, use partial balancing at Step 3 to write the Step 4 bridge. ©2008 ChemReview.net v. f9 Page 299 Module 14 — Acid-Base Neutralization • An unknown acid with 3 acidic protons can be written as H3Unk when balancing. If needed, adjust your work and finish from here. * * * * * 5. SOLVE. In stoichiometry, when a ratio unit is WANTED, solve separately for the top and bottom WANTED amounts in a sample, then divide. a. Label the DATA equality that has the two amounts that are equivalent at the endpoint as “Equivalent”or “2SUA-R.” b. Solve first for the easier unit (the one not moles), using as a given the side of the equivalency that contains the WANTED substance formula. In this problem, the WANTED amount not moles is g acid. The grams of acid in the sample are supplied in the equivalency. That was easy. ? g acid in sample = 0.1484 g acid c. To find the moles of acid WANTED, start with the other half of the equivalency as the given. * * * * * In this problem, the acid may be written as acid or as H3Unk . Start: ? mol acid = 19.29 mL KOH (other half of equivalency) Use single-unit stoichiometry. Convert to the moles of the given that reacted, ? mol WANTED = unit given >> ? mol acid = 19.29 mL KOH • mol given 1 L • 0.120 mol KOH • 1 L KOH 103 mL * * * * * Cross the mol/mol bridge to reach the moles of WANTED substance. ? mol WANTED = unit given >> mol given >> mol WANTED (stop) ? mol acid = 19.29 mL KOH • 1 L • 0.120 mol KOH • 1 mol acid = 1 L KOH 3 mol KOH 103 mL = 7.716 x 10─4 mol H3Unk in the sample. * * * * * Solve for the final WANTED ratio. ? g acid mol acid = g acid in sample mol acid in sample = 0.1484 g acid = ─4 7.716 x 10 mol acid 192 g acid mol The molar mass of a substance is constant: a ratio that is characteristic. The concentration of a well-mixed solution is a ratio that is constant. In cases where a ratio WANTED is constant, if the amounts of the top and bottom WANTED units in a sample can be found, that ratio will be true for all samples. * * * * * ©2008 ChemReview.net v. f9 Page 300 Module 14 — Acid-Base Neutralization Stoichiometry and CSI Consider what we were able to determine in the above calculation. Many molecules that are important in chemical and biological systems, including legal and illegal drugs, are acids or bases. In the above problem, we did not know the chemical formula for the acid. However, by finding the ratio of the grams of acid per mole of the acid (its molar mass), we can get close to identifying the acid. The acid can be weighed to find the grams in a sample, but nearly always we do not have a way to count the number of particles (the moles) in a sample directly. However, for acids and bases, we can determine the moles in a sample by titrating with an acid or base solution of a known concentration and applying stoichiometry. In titration, when the indicator changes color, the moles of two reacting particles are either equal or in a whole-number ratio. Knowing the grams and moles in a sample, we can find the grams to moles ratio: the molar mass. From the molar mass of a substance and its melting point or other physical constants, tables in chemistry reference media will identify many unknown substances with near certainty. The ability to identify an unknown acid or base is a skill that is marketable in forensic criminology, medicine, and other rewarding careers. Practice: If needed, review the steps for solving solution stoichiometry in Lesson 12C. Answers are at the end of this lesson. If you get stuck, read a portion of the answer until unstuck, then try again. 1. If 124 milliliters of a barium hydroxide solution is needed to completely neutralize 2.34 grams of arsenic acid (H3AsO4), what is the original [Ba(OH)2]? 2. A 2.00 M H3PO4 solution is completely neutralized by 1.50 liters of 0.500 M OH─. How many mL of the H3PO4 solution were neutralized? 3. Oxalic acid (90.03 g•mol─1) is a solid at room temperature. Each oxalic acid particle contains two acidic hydrogens. If 44.43 mL of an NaOH solution is needed to completely neutralize 0.100 g of oxalic acid crystals, find the [NaOH]. 4. Review Lessons 14A-C and prepare flashcards that cover the fundamentals. Take the Paper You Need In many problems, a methodical approach will require using an entire sheet of paper to solve each question. That’s OK. Paper recycles. Trees grow. Your understanding will also grow if you take the time and paper that is needed for careful work. If you are solving in a graph-paper notebook (a good idea), try working with the paper in the landscape mode (turned sideways). This provides more room for the long string of conversions that stoichiometry often requires. ©2008 ChemReview.net v. f9 Page 301 Module 14 — Acid-Base Neutralization ANSWERS 1. 1. WANTED: 2. DATA: ? mol Ba(OH)2 L soln (the unit WANTED is mol/L) 124 mL Ba(OH)2 soln. = 2.34 g H3AsO4 (equivalent at end point) 141.9 g H3AsO4 = 1 mol H3AsO4 (g prompt) (When stoichiometry WANTS a ratio unit, all of the data will be in equalities, and one equality will be two amounts that are equivalent at the endpoint. When reaction calculations involve two 2 substances, that’s the stoichiometry prompt. All stoichiometry begins with the same 4 steps: WDBB.) 3. Balance. (Using the rules in Lesson 14B,) 2 H3AsO4 + 3 Ba(OH)2 Æ 6 H―OH + … 4. Bridge. (use partial balancing) 2 mol H3AsO4 = 3 mol Ba(OH)2 5. SOLVE. (Since a ratio unit is WANTED, solve for the top and bottom WANTED amounts separately. a. Label the equivalency in the data. b. Solve for the easier WANTED amount first (usually the one not moles), using as a given the side of the equivalency that measures the WANTED substance.) ? L Ba(OH)2 = 124 mL Ba(OH)2 • 1 L = 0.1240 L Ba(OH)2 103 mL (move decimal 3 times) c. (To find the other WANTED unit (usually moles), use single-unit stoichiometry steps. Start with the other half of the equivalency as your given.) ? mol Ba(OH)2 = 2.34 g H3AsO4 • 1 mol H3AsO4 • 3 mol Ba(OH)2 = 0.02473 mol Ba(OH)2 141.9 g H3AsO4 2 mol H3AsO4 (Carry an extra sf until the final step. Finish, then check below. * * * * * d. Solve for the final WANTED unit using the two amounts found above.) ? mol Ba(OH)2 = mol Ba(OH)2 in sample = 0.02473 mol Ba(OH)2 = L soln L Ba(OH)2 in sample 0.1240 L Ba(OH)2 soln. 2. 0.200 mol Ba(OH)2 L Ba(OH)2 (For reaction calculations, use stoichiometry steps. Stoichiometry starts with WDBB.) WANT: ? mL H3PO4 DATA: 2.00 mol H3PO4 = 1 L H3PO4 1.50 L OH─ soln. 0.500 mol OH─ = 1 L OH─ (you want a single unit) (M prompt) (the single unit given) (M prompt) (Since you have solutions of two different substances, include formulas after all units to identify the substance that each number and unit measures. Since all volumes in the problem are for aqueous solutions, you may label one volume as “soln.” but omit the other “solution” labels as “understood.”) ©2008 ChemReview.net v. f9 Page 302 Module 14 — Acid-Base Neutralization Balance: 1 H3PO4 + 3 OH─ Æ 3 H2O + PO43─ Bridge. 1 mol H3PO4 = 3 mol OH─ SOLVE: Since a single unit is WANTED, use single-unit stoichiometry, chaining conversions.) ? mL H3PO4 = 1.50 L OH─ • 0.500 mol OH─ • 1 mol H3PO4 • 1 L H3PO4 • 103 mL = 1 L OH─ 3 mol OH─ 2.00 mol H3PO4 1 L = 125 mL H3PO4 3. WANTED: ? mol NaOH L NaOH soln DATA: 44.43 mL NaOH = 0.100 g oxalic acid (Equivalent at endpoint) 90.03 g oxalic acid = 1 mol oxalic acid Balance: Let oxalic acid be H2Unk. Bridge. 1 H2Unk + 2 NaOH Æ 2 H2O + …. 1 mol H2Unk = 2 mol NaOH SOLVE. (Not moles): ? L NaOH = 44.43 mL NaOH = 0.04443 L NaOH (by inspection) (moles): ? mol NaOH = 0.100 g H2Unk • 1 mol acid • 2 mol NaOH = 2.221 x 10─3 mol 90.03 g acid 1 mol acid NaOH ? = mol NaOH = L NaOH 2.221 x 10─3 mol NaOH = 0.04443 L NaOH soln. 0.0500 mol NaOH L NaOH 4. Your flashcards might include the following. One-way cards (with notch) Names and formulas for 3 strong acids Back Side -- Answers Hydrochloric: HCl, sulfuric: H2SO4, nitric: HNO3 Ion symbol for a proton H+ At the endpoint of acid-hydroxide neutralization Moles H+ = moles OH─ Formula for an unknown base with 3 hydroxides Unk(OH)3 Formula for an unknown with 2 acidic protons H2Unk Two-way cards (without notch): An acid A substance that produces H+ in water A base A substance that neutralizes H+ 3 moderate to strong basic ions used in neutralization OH─, CO32─, HCO3─ * * * * * ©2008 ChemReview.net v. f9 Page 303 Module 14 — Acid-Base Neutralization Lesson 14D: Neutralization Calculations In Parts Timing: Do this lesson if you are assigned neutralization calculations that include either measurements for three particles or questions with multiple parts. * * * * * Calculations Involving Both Ionized and Un-Ionized Acids or Base Formulas For neutralization calculations that include data for both un-ionized acid or base formulas and their reacting ions, you will need to write a relationship between the ionized and unionized particles. Use this special rule. 1. In stoichiometry, when the WANTED and DATA include units that measure both an solid formula and its ions, a. write the balanced reaction equation in three parts: Reactants in molecular formulas Æ Reactants as separated ions Æ Products b. In the bridge conversion, write all formulas in the WANTED and DATA that have units attached. (This may result in three or more terms that are equal in the bridge conversion, instead of two.) If a unit with a chemical formula attached is written in the WANTED or DATA, it represents a measured quantity. To solve, mole to mole relationships are needed among all of the measured quantities. We find those relationships from the coefficients of the balanced equation. There are other ways to track the relationship between particles and their ions, but the above rules have the advantage of being consistent with both the rule for precipitation reactions and our fundamental rule for reactions that involve ions: To understand the reactions of ionic compounds, write the reactants as separated ions, then look for possible reactions in the new mixture of ions. Use Rule 1 to solve the following. Q. A sample of 15.0 mL of Ba(OH)2 solution is neutralized by 28.14 mL of 0.100 M HCl. What was the [OH─] in the original base solution? Write only the first four stoichiometry steps, then check your answer below. * * * * * Answer: Your paper should look like this. 1. WANT: ? mol OH─ L OH─ 2. DATA: 15.0 mL Ba(OH)2 = 28.14 mL HCl 0.100 mol HCl ©2008 ChemReview.net v. f9 = (Equivalent at endpt. -- 2SUA-R) 1 L HCl Page 304 Module 14 — Acid-Base Neutralization 3. Balance. Reactants – molecular: 1 Ba(OH)2 + 2 HCl Æ Reactants as ions: Æ 1 Ba2+ + 2 OH─ + 2 H+ + 2 Cl─ Æ Products: 4. Bridge: Æ 2 H2O + …. 1 mol Ba(OH)2 = 2 mol HCl = 2 mol OH─ * * * * * Rules that apply above include • In stoichiometry for a ratio unit, two amounts will be equivalent at the endpoint. • In acid-base stoichiometry, the WANTED and DATA are nearly always measurements of the two reactants. You will only need to know one product formula to find the coefficients for the reactants. • In the WANTED and DATA there are three chemical formulas with units in front: OH─, Ba(OH)2, and HCl. This is a prompt to balance the equation in 3 parts. An additional prompt is that the OH─ ion must come from the Ba(OH)2. When the WANTED and DATA include both an un-ionized formula and one or more of its ions, write the balanced equation in 3 parts: solid formulas, separated ions, products (in neutralization, one product). • In step 4, include in the bridge conversion the moles of all the chemical formulas in the WANTED and DATA that were listed after units of measure. This problem has three such formulas. Now solve for the WANTED unit. * * * * * To solve a reaction calculation for a ratio, solve for top and bottom WANTED units separately, then divide. a. Label the DATA equality that has two amounts equivalent at the endpoint as “Equivalent”or “2SUA-R.” b. Solve first for the easier unit (the one not moles), using as a given the side of the equivalency that measures the WANTED chemical formula. In this problem, the WANTED unit not moles is L OH─. In the DATA equivalency is mL of Ba(OH)2 solution. Since the solution labeled Ba(OH)2 is the solution that contains the OH─ ions, the Ba(OH)2 and OH─ solutions are the same solution. The moles of Ba(OH)2 and OH─ differ, but the volume of the solution in which those chemical formulas are found in the same. ? L OH─ soln. = 15.0 mL Ba(OH)2 soln. = 0.0150 L Ba(OH)2 = 0.01500 L OH─ If needed, adjust your work and finish. * * * * * ©2008 ChemReview.net v. f9 Page 305 Module 14 — Acid-Base Neutralization c. Solve for the other WANTED unit using single-unit stoichiometry. Use the other half of the equivalency as your given. Use the bridge to go from given to WANTED. ? mol OH─ = 24.18 mL HCl ● 1 L HCl ● 0.100 mol HCl ● 1 mol OH─ 1 L HCl 2 mol HCl 103 mL = 1.209 x 10─3 mol OH─ = (carry an extra sf until the final step) d. Solve for the final WANTED unit. * * * * * ? mol OH─ = 1.209 x 10─3 mol OH─ = L OH─ 0.01500 L OH─ 0.0806 mol OH─ L OH─ * * * * * Neutralization Calculations in Parts When problems contain more than one question about a common set of DATA, the general rules (from Lesson 11F) included • First list the common DATA, then write the WANTED unit for each part. As parts are completed, consider those answers to be additional DATA. Similarly, for reaction calculations that have multiple questions, use special rule 2. 2. When stoichiometry contains more than one question about a common set of data, • First do stoichiometry steps 2, 3, and 4 (DATA, balance, bridge), • then do step 1(WANTED) for each part. Stoichiometry that has multiple questions will also rely on these previous rules. • To solve for single units when all of the data is in equalities, label the DATA as SUA, R, or 2SUA-R (Lesson 11F). Use single-unit amounts (SUA or 2SUA-R), not ratios, as a given to solve for single units. • To solve for a single unit, try to select a given from the SUA DATA that solves in the fewest steps. Include as DATA answers from previous steps. A Shortcut: Moles H+ = Moles OH─ When a stoichiometry problem asks questions in multiple parts, each part can be treated as a separate new problem in which you “start over” to solve. However, the parts of a problem can often be solved more quickly by using answers to previous parts plus fundamental relationships. A fundamental equality that can be used in acid-hydroxide reactions is special rule 3. 3. In hydroxide neutralization, some steps may be solved by inspection using this rule: At the equivalence point, the moles of H+ in the original acid sample equal the moles of OH─ in the original base sample. At the endpoint of acid-OH─ titration, mol H+ reacted = mol OH─ reacted ©2008 ChemReview.net v. f9 Page 306 Module 14 — Acid-Base Neutralization Use special rules 1, 2, and 3 to solve the following problem. Q. KH(IO3)2 (potassium hydrogen iodate – 389.9 g/mol) is a primary standard solid acid that can be used to determine the concentration of base solutions. In such a titration, the indicator changes color when 19.29 mL of a KOH solution has been added to 0.338 grams of KH(IO3)2. A. How many moles of H+ ions were in the acid sample? B. C. * * * * * Answer How many moles of hydroxide ions were in the added base sample? Find the [KOH]. 2. DATA: 389.9 g KH(IO3)2 = 1 mol KH(IO3)2 19.29 mL KOH = 0.338 g KH(IO3)2 (R) (2SUA-R - equivalent at endpt.) 3. Balance: Solid formulas: 1 KH(IO3)2 + 1 KOH Æ Separated formulas: Æ 1 K+ + 1 H+ + 2 IO3─ + 1 K+ + 1 OH─ Æ Products: 4. Bridge: Æ 1 H2O + …. 1 mol KH(IO3)2 = 1 mol KOH = 1 mol H+ = 1 mol OH─ The above uses Partial balancing with one product will find the neutralization bridge conversions. Rule 3: For stoichiometry that asks several questions, first complete steps 2, 3 and 4, then do step 1 for each part. Rule 1: This problem and its parts includes measurements for four particles: KH(IO3)2 , KOH, H+, and OH─. When the WANTED and DATA includes both solid/molecular formulas and ions, write the balanced equation in three parts: reactants in molecular (solid) formulas, reactants as separated-ions, then products using formulas for the substances and ions actually present in the products. When solving a problem with parts, you may not catch that both ions and molecular formulas are both included until reaching a later part of a problem. If that happens, add the 3-part balancing step to the DATA at that time. In the bridge conversion, include all of the particle formulas that label units in the DATA and WANTED terms, including WANTED units found in later parts of the problem. Solve Part A. * * * * * ©2008 ChemReview.net v. f9 Page 307 Module 14 — Acid-Base Neutralization Part A: WANT: ? mol H+ Strategy: WANT a single unit? Start with a single unit. Since all of the DATA is in equalities, pick one of the single-unit amounts, from the two that are equivalent, as your given. Pick the amount that you can most easily convert to the WANTED mol H+. * * * * * The H+ ions are formed from KH(IO3)2 in this reaction: 1 mol KH(IO3)2 Æ 1 mol H+ + ….. Since this is a reaction, try stoichiometry steps using the known amount of KH(IO3)2 as your given. * * * * * amount known bridge relationship ? mol H+= 0.338 g KH(IO3)2• 1 mol KH(IO3)2 • 1 mol H+ = 389.9 g KH(IO3)2 1 mol KH(IO3)2 8.669 x 10─4 mol H+ Carry an extra sf until the last part. Add this answer to the DATA. Using the Part A answer, try solving Part B by inspection. * * * * * Part B: WANT: ? mol OH─ In problems with parts, watch for easy conversions from answers to earlier parts. At the endpoint of an acid-hydroxide titration, when the indicator changes color: moles H+ reacted = moles OH─ reacted. Using the Part A answer: ? mol OH─ = 8.669 x 10─4 mol H+ = 8.669 x 10─4 mol OH─ Once you know the moles of either H+ or OH─, you know the moles of the other in the sample. Part C: WANT: ? mol KOH L KOH soln. We solve stoichiometry for a ratio in three steps: find the top amount, bottom amount, and divide. Try solving for the first two of those three steps by inspection. * * * * * You could start at the beginning and do complete ratio-unit stoichiometry, but using answers found so far will save steps. For the top WANTED unit: 1 mole KOH Æ 1 mole OH─ , so from Part B, 8.669 x 10─4 moles OH─ = 8.669 x 10─4 mol KOH in the sample. * * * * * ©2008 ChemReview.net v. f9 Page 308 Module 14 — Acid-Base Neutralization For the bottom unit (L KOH in the sample), the mL KOH in the sample is known. By inspection, moving the decimal 3 times, Bottom unit = ? L KOH = 19.29 mL KOH = 0.01929 L KOH Find the final WANTED ratio. * * * * * If you want a ratio, you must convert from a ratio. The answer unit divides the moles KOH in the sample by the L KOH in the sample. Both of those amounts are solved above. WANT: ? mol KOH = L KOH 8.669 x 10─4 mol KOH = 0.01929 L KOH 0.0449 mol KOH L KOH In the original DATA, 0.338 g has 3 sf. This limits the final answer to 3 sf. Practice. Do Problem 1 today. Save Problem 2 for your next study session. 1. A 10.00 mL sample of NaOH solution completely neutralizes 55.1 mg H2SO4. a. How many moles of H2SO4 were neutralized? b. What was the original concentration of the base solution? 2. If 10.91 mL of 0.110 M HCl is required to neutralize 25.00 mL of Ba(OH)2 solution, a. how many moles of hydroxide ions were in the original base solution ? b. What was the original [base]? ANSWERS 1. (For reaction calculations with parts, do stoichiometry steps 2, 3, 4, then 1) 2. DATA: 10.00 mL NaOH = 55.1 mg H2SO4 98.1 g H2SO4 = 1 mol H2SO4 3. Balance: 4. Bridge. 2 NaOH + 1 H2SO4 Æ 2 H2O + ….. 2 mol NaOH = 1 mol H2SO4 (equivalent at endpoint) ( mg = g prompt) (partial balancing provides the bridge) WANT: ? mol H2SO4 Part A: * * * * * (Using the rules in Lesson 11F: if you want a single unit and all of the DATA is in equalities, • Label the equality that has two amounts that are equivalent; • Choose one side of the equivalency as the given; • As the given, pick the side that most easily converts to the WANTED unit. In stoichiometry, that will usually be the side of the equivalency that has the WANTED formula.) ? mol H2SO4 = 55.1 mg H2SO4 • 1 g • 1 mol H2SO4 = 5.617 x 10─4 mol H2SO4 103 mg 98.1 g H2SO4 * * * * * ©2008 ChemReview.net v. f9 Page 309 Module 14 — Acid-Base Neutralization Part B: WANT: ? mol NaOH L NaOH soln (non-moles): (solve for non-moles, then moles) ? L NaOH soln. = 10.00 mL NaOH = 0.01000 L NaOH (Solve for moles NaOH: You can use stoichiometry steps, or use the Part A answer to solve more quickly. The moles of acid from Part A are known. Mol/mol ratios for reactions are always simple. Here, the moles of base that reacts is 2x the moles of acid that reacts.) ? mol NaOH = 5.617 x 10─4 mol H2SO4 • 2 = 11.23 x 10─4 mol NaOH in sample * * * * * ? mol NaOH = 11.23 x 10─4 mol NaOH in sample = L NaOH 0.01000 L NaOH in sample 0.112 mol NaOH L NaOH (Original DATA has 3 sf or higher; round the final answer to 3 sf) 2. (For reaction calculations with parts, do stoichiometry steps 2, 3, and 4 first.) 2. DATA: 25.00 mL of Ba(OH)2 = 10.91 mL HCl (Equivalent at endpoint) 0.110 mol HCl = 1 L HCl soln. 3. Balance: (Since the problem includes quantities of both Ba(OH)2 and OH─ , balance in 3 parts.) 2 HCl + 1 Ba(OH)2 Æ 2 H+ + 2 Cl ─ + Ba2+ + 2 OH─ Æ 2 H2O + 1 BaCl2 4. Bridge: 2 mol HCl = 1 mol Ba(OH)2 = 2 mol OH─ Part A. WANT: ? moles OH─ (There are several ways to solve, but whenever moles of H+ or OH─ are involved in a problem, consider using the rule that 1 mol H+ neutralizes 1 mol OH─. Take a look at the DATA. Can you find moles of OH─ or base directly? No. But you know a lot about the HCl. If you can find moles of HCl that reacted, that equals the moles of H+ that reacted (1 HCl Æ 1 H+), which equals the moles of OH─ that reacts.) * * * * * ? mol HCl = 10.91 mL HCl • 1 L • 0.110 mol HCl = 1.20 x 10─3 mol HCl = mol H+ = mol OH─ 103 mL 1 L HCl soln. Part B: WANT: ? mol Ba(OH)2 L Ba(OH)2 (non-moles) (solve stoichiometry ratios for non-moles, then moles) ? L Ba(OH)2 soln. = 25.00 mL Ba(OH)2 = 0.02500 L Ba(OH)2 (Find moles Ba(OH)2: You can use stoichiometry or you can solve by inspection. Since 1 Ba(OH)2 Æ 2 OH─ , the mol Ba(OH)2 is 1/2 the mol OH─ from Part A.) ? mol Ba(OH)2 = 1/2 times 1.20 x 10─3 mol OH─ = 0.600 x 10─3 mol Ba(OH)2 (Finish from here.) ©2008 ChemReview.net v. f9 Page 310 Module 14 — Acid-Base Neutralization * * * * * ? mol Ba(OH)2 L Ba(OH)2 * * * * * = 6.00 x 10─4 mol Ba(OH)2 = 0.02500 L Ba(OH)2 soln. 0.0240 mol Ba(OH)2 L Ba(OH)2 Lesson 14E: Carbonate Neutralization Timing: Do this lesson if you are assigned problems involving the acid-base neutralization of carbonates and/or hydrogen carbonates. Prerequisites: Lessons 7C, 12C, and 14A. Pretest: If you can do all steps of the following problem, you may skip this lesson. Check answers at the end of this lesson. Q. Assuming complete neutralization of all protons and basic ions in an open system, write the final product formulas and balance these. a. CaCO3 + HCl Æ b. c. H2SO4 + Al2(CO3)3 Æ HCO3─ + OH─ Æ d. HCO3─ + H+ Æ * * * * * Carbonic Acid At room temperature and pressure, CO2 gas dissolves to a slight extent in water. If pressure is applied to a CO2 gas and water mixture, more gas dissolves. This pressurized mixing is used to make carbonated beverages. Some CO2 molecules, when dissolved in water, react with water form carbonic acid: H2CO3(aq). Carbonic acid is a weak acid. In water, it ionizes to form H+ plus HCO3─, but it does so only slightly; less than 1% of the carbonic acid molecules ionize at room temperature. The dissolved CO2 gas gives carbonated beverages their effervescence, and the H+ ions, though low in concentration, give carbonated beverages their tart (acidic) taste. Together, these reactions can be represented as H2O(l) + CO2(g) Å Æ H2CO3(aq) Å Æ H+(aq) + HCO3─(aq) The two-way arrows indicate that these reactions are reversible: the steps can go forward and backward. Kept under pressure at constant temperature, a carbonated solution is a stable mixture of all of the particles above. However, if the solution is left open at room pressure, the CO2 gas will slowly leak out. This “drives the reaction to the left,” using up the H+, HCO3─, and H2CO3. As the CO2 gas leaves, the solution loses its fizz and acid tartness. ©2008 ChemReview.net v. f9 Page 311 Module 14 — Acid-Base Neutralization Hydrogen Carbonate Ion A second way to make a carbonic acid solution is to react an acid with hydrogen carbonate ion (HCO3─, also known as bicarbonate ion). The result is the same two-way reaction written above, but it is usually written in the reverse direction to emphasize the addition of acid to the HCO3─. H+ + HCO3─ ÅÆ [ H2CO3 ] Å Æ H2O + CO2↑ When CO2 is mixed with water, carbonic acid forms slowly and a low concentration, but when typical lab concentrations of acid and HCO3─ are mixed, the carbonic acid forms quickly and at relatively high concentration compared to its formation by mixing carbon dioxide and water. At room pressure, most of the carbonic acid formed will quickly break down into water and carbon dioxide gas. The mixing of acid and hydrogen carbonate ion thus causes the solution to form bubbles of CO2 gas. In the reaction above, the brackets [ ] are a way to indicate a substance is formed temporarily. When acid and hydrogen carbonate are mixed, most of the carbonic acid formed is an intermediate particle that quickly breaks apart. If the container is open, the up-arrow ↑ after the CO2 is one way to indicate that a gas formed is allowed to escape. In the reaction above, HCO3─ reacts with an acid as a base. However, HCO3─ is amphoteric, meaning that it can react with both acids and bases. How it behaves will depend on whether it is mixed with an acid or a base. • Mixed with an acid: H+ + HCO3─ Æ • Mixed with a base: OH─ + HCO3─ Æ H─OH + CO32─ [ H2CO3 ] Æ H2O + CO2↑ When HCO3─ is mixed with acids, it forms H2CO3 and then CO2 gas. When HCO3─ is mixed with a strong base such as OH─, it loses a proton to form carbonate ion, and the solution does not bubble. Practice A Check answers as you go. 1. Predict intermediate (if any) and final products of these reactions in open containers, then balance the equations. Ion combinations in final products may be written in solid or separated formulas. a. HCl + NaHCO3 b. HCO3─ + c. Sodium hydroxide plus sodium hydrogen carbonate Æ d. LiHCO3 + ©2008 ChemReview.net v. f9 Æ H2SO4 Æ OH─ Æ Page 312 Module 14 — Acid-Base Neutralization Carbonate Neutralization A third way to make a carbonic acid solution is to react excess acid with carbonate ion (CO32─), a base. In the complete neutralization of CO32─, one product is always H2CO3. As in the reaction of acid and hydrogen carbonate, if carbonate ion is reacted with excess acid in an open container, the carbonic acid formed it will quickly break down to form water and bubbles of carbon dioxide. 2 H+ + CO32─ [ H2CO3 ] Å Æ H2O + CO2↑ If acid is slowly mixed with CO32─ ions, HCO3─ ions form initially. Once equivalent moles of carbonate and protons are mixed, all of the carbonate ion is converted to hydrogen carbonate ion, and further addition of acid forms H2CO3, most of which breaks down quickly into water and CO2 gas. ÅÆ Complete Balancing of Acid-Carbonate Neutralization To predict the complete products for the reaction of acids with CO32─ or HCO3─, use these rules. • If an acid reacts with HCO3─ or completely neutralizes CO32─, one product is H2CO3. • H2CO3 breaks apart to form liquid H2O and CO2 gas. When representing all of the products carbonate neutralization in equations, it is helpful to balance the equation in five steps. For example: Calcium carbonate is found in minerals including limestone, calcite, chalk, and marble. When excess hydrochloric acid solution is added to calcium carbonate, the solution bubbles. Why? Step 1. Write molecular formulas: 2 HCl + CaCO3 Æ Step 2. Separate reactants into ions: Æ 2 H+ + 2 Cl─ + Ca2+ + CO32─ Æ Step 3. Write the initial products: Æ [ H2CO3 ] + Ca2+ + 2 Cl─ Æ When excess acid mixes with carbonate ion, one of the products is H2CO3. Step 4. Write final products: Æ H2O + CO2↑ + CaCl2(aq) Step 5. Check that the atoms and total charge are balanced in all parts. The fundamental rule: to predict the reactions of ionic compounds, re-write the solid and molecular formulas for the reactants as separated ions, then look for ways that the new possible combinations of ions will react. In the final step, the spectator ions in the products can be represented by either an ionic solid formula labeled aqueous or as the separated ions actually present. Ca2+ + 2 Cl─ = CaCl2(aq) * * * * * ©2008 ChemReview.net v. f9 Page 313 Module 14 — Acid-Base Neutralization Practice B: Assume that these acids and bases ionize and react completely. Write balanced equations for the steps of the reaction using the 5 step method above. Ions in final products may be written in solid or separated formulas. Check answers as you go. 1. Write formulas for reactants (if needed) and products, then balance the equation. a. HCl + K2CO3 b. CO32─ + c. Sulfuric acid plus sodium hydrogen carbonate Æ Æ H3PO4 Æ Partial Balancing of Carbonate Neutralization To solve most neutralization stoichiometry, we only need the coefficients of the acid and the base. This partial balancing can be completed if know the formula for one product. In the complete neutralization of HCO3─ or CO32─ by acid, one product is always H2CO3. For this problem, write H2CO3 as one product, balance the left side, and then check below. Q. What is the ratio of reaction for H2SO4 + Al2(CO3)3 Æ * * * * * 1. Below the two reactants, write the number of protons and basic ions in the reactants. 2. On the right, add one product of the reaction. H2SO4 + Al2(CO3)3 Æ H2CO3 + … ( 2 H+ ) + (3 CO32─ ) Æ H2CO3 + … 3. Add coefficients to balance the atoms and charge. H2SO4 + Al2(CO3)3 3 ( 2 H+ ) + Æ 1 (3 CO32─ ) H2CO3 + … Æ 3 H2CO3 + … 4. Transfer the coefficients in front of the ( ) to the reactants. 3 H2SO4 + 1 Al2(CO3)3 Æ 3 H2CO3 + … 3 ( 2 H+ ) + 1 (3 CO32─ ) Æ 3 H2CO3 + … The top reactant ratio will be all that is needed in most neutralization stoichiometry. Knowing one product, and with practice at separating molecular formulas into ions, you can often balance the reactants by inspection. Try that on this one. Q. What is the ratio of reaction for HNO3 + BaCO3 Æ * * * * * One product for acid-carbonate neutralization is H2CO3. Add the coefficients by inspection. 2 HNO3 + 1 BaCO3 Æ 1 H2CO3 + … * * * * * ©2008 ChemReview.net v. f9 Page 314 Module 14 — Acid-Base Neutralization Practice C First review the rules in the summary at the end of this module. Then try these problems. Assume that the following acids and bases react completely. Balance the acid and base reactants using the partial balancing methods above. Try every other part, and more if you need more practice. Check answers as you go. 1. Write formulas for reactants (if needed) and products, then balance the equation. a. HNO3 + Al2(CO3)3 Æ b. Calcium carbonate plus nitric acid Æ c. Potassium hydroxide plus potassium hydrogen carbonate Æ 2. Supply the coefficients for the two reactants. a. H2Unk + NaHCO3 Æ b. H2SO4 + Unk(CO3)3 Æ c. HCl + Unk(CO3)2 Æ Carbonate and Hydrogen Carbonate Neutralization Calculations In carbonate and hydrogen carbonate neutralization, the ratio of reaction for the acid and the base can be determined by partial balancing using the steps above. Once those acid and base coefficients are known, neutralization calculations can be solved using the same solution stoichiometry steps that were practiced in Lesson 12C and 14D. If needed, refer to those steps when solving the problems below. Practice D: Answers are at the end of this lesson. If you get stuck, read a portion of the answer until you are unstuck, then try again. 1. If 38.58 mL of 0.150 M HCl is needed to react completely with a sample of solid CaCO3, how many grams of calcium carbonate were in the sample? 2. If 872 mg of a dry solid acid is neutralized by 24.0 mL of 0.150 M NaHCO3, assuming that each acid particle contains two acidic hydrogens, what is the molar mass of the acid? 3. Review Lessons 14D-E and write additional flashcards that cover the fundamentals. ©2008 ChemReview.net v. f9 Page 315 Module 14 — Acid-Base Neutralization ANSWERS Pretest: Coefficients of 1 may be omitted as understood. a. 1 CaCO3 + 2 HCl Æ 1 H2O + 1 CO2↑ + 1 CaCl2 b. 3 H2SO4 + 1 Al2(CO3)3 Æ 3 H2O + 3 CO2↑ + 1 Al2(SO4)3 c. HCO3─ + OH─ Æ H2O + CO32─ d. HCO3─ + H+ Æ 1 H2O + 1 CO2↑ Practice A: Balance atoms and charge in all parts of each equation. Coefficients of 1 may be omitted. 1. a. b. 1 HCl + 1 NaHCO3 Æ 1 [ H2CO3 ] + 1 NaCl Æ H2O + CO2↑ + NaCl 2 HCO3─ + 1 H2SO4 Æ 2 [ H2CO3 ] + SO42─ Æ 2 H2O + 2 CO2↑ + SO42─ c. 1 NaOH + 1 NaHCO3 Æ 1 H─OH + 1 Na2CO3 d. 1 LiHCO3 + 1 OH─ Æ 1 H─OH + 1 Li+ + 1 CO32─ Practice B: Balance atoms and charge in all 4 parts of each equation. 2 H+ + 2 Cl─ + 2 K+ + CO32─ Æ Æ 1 [ H2CO3 ] + 2 KCl Æ H2O + CO2↑ + 2 KCl 1. a. 2 HCl + 1 K2CO3 Æ b. 3 CO32─ + 2 H3PO4 Æ 3 CO32─ + 6 H+ + 2 PO43─ Æ Æ 3 [ H2CO3 ] + 2 PO43─ Æ 3 H2O + 3 CO2↑ + 2 PO43─ c. 1 H2SO4 + 2 NaHCO3 Æ 2 H+ + 1 SO42─ + 2 Na+ + 2 H+ + 1 CO32─ Æ Æ 2 [ H2CO3 ] + 1 Na2SO4 Æ 2 H2O + 2 CO2↑ + 1 Na2SO4 Practice C 1. a. 6 HNO3 + 1 Al2(CO3)3 Æ 3 [ H2CO3 ] + … b. 1 CaCO3 + 2 HNO3 Æ 1 [ H2CO3 ] + … c. 1 KOH + 1 KHCO3 Æ H─OH + CO32─ … (mixed with OH─, HCO3─ acts as an acid) 2. a. 1 H2Unk + 2 NaHCO3 Æ 2 [ H2CO3 ] + … b. 3 H2SO4 + 1 Unk(CO3)3 Æ 3 [ H2CO3 ] + … c. 4 HCl + 1 Unk(CO3)2 Æ 2 [ H2CO3 ] + … Practice D 1. 1. WANT: ? g CaCO3 2. DATA: 100.1 g CaCO3 = 1 mol CaCO3 38.58 mL HCl 0.150 mol HCl = 1 L HCl soln. ( g prompt) (the single unit given) (M prompt) (For a reaction with DATA for two substances, use stoichiometry steps. Start with WDBB) ©2008 ChemReview.net v. f9 Page 316 Module 14 — Acid-Base Neutralization 3. Balance. (For acid-base neutralization, try partial balancing – reactants only.) 1 CaCO3 + 2 HCl Æ 1 [H2CO3] + ….. 4. Bridge. 1 mol CaCO3 Æ 2 mol HCl * * * * * (Since a single unit is WANTED, use single-unit stoichiometry steps 5-7, chaining the conversions.) ? g CaCO3 = 38.58 mL HCl • 1 L • 0.150 mol HCl • 1 mol CaCO3 • 100.1 g CaCO3 = 0.290 g CaCO3 1 L HCl 2 mol HCl 1 mol CaCO3 103 mL (Write the unit WANTED) 2. 1. WANTED: g acid mol acid 2. DATA: 872 mg acid = 24.0 mL NaHCO3 (Equivalent at endpoint) 0.150 mol NaHCO3 = 1 L NaHCO3 (M prompt) 3. Balance. Let acid with two acidic hydrogens = H2Unk 1 H2Unk + 2 NaHCO3 Æ 2 [H2CO3] + …. 4. Bridge. 1 mol H2Unk (or 1 mol acid) = 2 mol NaHCO3 5. SOLVE. (Not moles): ? g acid = 872 mg acid • (Moles): = 1g 103 mg 0.872 g acid in sample ? mol acid = 24.0 mL NaHCO3 • 1 L • 0.150 mol NaHCO3 • 1 mol acid = 103 mL 1 L NaHCO3 2 mol NaHCO3 = 1.800 x 10─3 mol acid in sample. WANTED: ? g acid mol acid = 0.872 g acid 1.800 x 10─3 mol acid = 484 g acid mol acid 3. Your flashcards might include the following. One-way cards (with notch) Back Side -- Answers Product of complete carbonate neutralization H2CO3 [ H2CO3 ] Breaks down to form H2O and CO2 Two-way cards (without notch): If stoichiometry WANTED and DATA includes both solid formulas and ions Write solid formulas Æ separated-ions Æ products Define amphoteric A particle that can act as an acid or a base ©2008 ChemReview.net v. f9 Page 317 Module 14 — Acid-Base Neutralization SUMMARY: Acid-Base Neutralization 1. Acid-base neutralization is an ionic reaction. To understand ionic reactions, write the separated-ion formulas, then look for new ion combinations that react. 2. Ions: Acids contain H+. The reacting particle in acids = H+ = a proton. Bases include compounds with hydroxide OH─, carbonate CO32─, and hydrogen carbonate HCO3─ ions. 3. Products: For acids + OH─, one product is water: H-OH. H+ + OH─ Æ H-OH For excess acid plus CO32─, one product is H2CO3. 2 H+ + CO32─ Æ H2CO3 4. Balancing: To predict the products and balance the equations, • Write the separated-ion formulas in ( ). • Write one product. • Finish by balancing atoms, familiar ions, and charge. 5. To balance if a formula is unknown, • If an acid has 2 acid hydrogens, use H2Unk. • If a base has 3 hydroxides, write Unk(OH)3. • If a base has 1 carbonate ion, use UnkCO3. If three, use Unk(CO3)3. 6. Stoichiometry: Do partial balancing at Step 3. Add one product; balance the left side, and use the left side numbers to write the key bridge conversion. 7. To solve acid-base calculations, use stoichiometry steps plus these 3 rules. 1. When the WANTED and DATA terms include units and particle formulas that include both an un-ionized particle and its ions, a. balance the reaction equation in three parts: Reactants in molecular formulas Æ Reactants in separated ions ÆProducts b. In the bridge conversion, write all formulas in the WANTED and DATA that have units attached. 2. In the case of stoichiometry problems that contain more than one question about a common set of data, • first do stoichiometry steps 2, 3, and 4, • then do step 1 (list the WANTED unit) for each part. 3. Hydroxide neutralization steps can often be solved by inspection using this rule: At the endpoint of acid-OH─ titration, mol H+ reacted = mol OH─ reacted # # # # ©2008 ChemReview.net v. f9 Page 318 Module 16: Half-Reaction Balancing * * * * * NOTE on the Table of Elements. The atomic masses in this Table of Elements use fewer significant figures than most similar tables in college textbooks. By keeping the numbers simple, it is hoped that you will use mental arithmetic to do easy numeric cancellations and simplifications before you use a calculator for arithmetic. Many calculations in these lessons have been set up so that you should not need a calculator at all to solve, if you look for easy cancellations first. After any use of a calculator, use mental arithmetic and simple cancellations to estimate the answer, in order to catch errors in calculator use. # # # # # ©2008 ChemReview.net v. f9 Page 356 The ELEMENTS – The third column shows the atomic number: The protons in the nucleus of the atom. The fourth column is the molar mass, in grams/mole. For radioactive atoms, ( ) is the molar mass of most stable isotope. Actinium Aluminum Americium Antimony Argon Arsenic Astatine Barium Berkelium Beryllium Bismuth Boron Bromine Cadmium Calcium Californium Carbon Cerium Cesium Chlorine Chromium Cobalt Copper Curium Dysprosium Erbium Europium Fermium Fluorine Francium Gadolinium Gallium Germanium Gold Hafnium Helium Holmium Hydrogen Indium Iodine Iridium Iron Krypton Lanthanum Lawrencium Lead Lithium Lutetium Magnesium Ac Al Am Sb Ar As At Ba Bk Be Bi B Br Cd Ca Cf C Ce Cs Cl Cr Co Cu Cm Dy Er Eu Fm F Fr Gd Ga Ge Au Hf He Ho H In I Ir Fe Kr La Lr Pb Li Lu Mg 89 13 95 51 18 33 84 56 97 4 83 5 35 48 20 98 6 58 55 17 24 27 29 96 66 68 63 100 9 87 64 31 32 79 72 2 67 1 49 53 77 26 36 57 103 82 3 71 12 (227) 27.0 (243) 121.8 39.95 74.9 (210) 137.3 (247) 9.01 209.0 10.8 79.9 112.4 40.1 (249) 12.0 140.1 132.9 35.5 52.0 58.9 63.5 (247) 162.5 167.3 152.0 (253) 19.0 (223) 157.3 69.7 72.6 197.0 178.5 4.00 164.9 1.008 114.8 126.9 192.2 55.8 83.8 138.9 (257) 207.2 6.94 175.0 24.3 Manganese Mendelevium Mercury Molybdenum Neodymium Neon Neptunium Nickel Niobium Nitrogen Nobelium Osmium Oxygen Palladium Phosphorus Platinum Plutonium Polonium Potassium Praseodymium Promethium Protactinium Radium Radon Rhenium Rhodium Rubidium Ruthenium Samarium Scandium Selenium Silicon Silver Sodium Strontium Sulfur Tantalum Technetium Tellurium Terbium Thallium Thorium Thulium Tin Titanium Tungsten Uranium Vanadium Xenon Ytterbium Yttrium Zinc Zirconium Mn Md Hg Mo Nd Ne Np Ni Nb N No Os O Pd P Pt Pu Po K Pr Pm Pa Ra Rn Re Rh Rb Ru Sm Sc Se Si Ag Na Sr S Ta Tc Te Tb Tl Th Tm Sn Ti W U V Xe Yb Y Zn Zr 25 101 80 42 60 10 93 28 41 7 102 76 8 46 15 78 94 84 19 59 61 91 88 86 75 45 37 44 62 21 34 14 47 11 38 16 73 43 52 65 81 90 69 50 22 74 92 23 54 70 39 30 40 54.9 (256) 200.6 95.9 144.2 20.2 (237) 58.7 92.9 14.0 (253) 190.2 16.0 106.4 31.0 195.1 (242) (209) 39.1 140.9 (145) (231) (226) (222) 186.2 102.9 85.5 101.1 150.4 45.0 79.0 28.1 107.9 23.0 87.6 32.1 180.9 (98) 127.6 158.9 204.4 232.0 168.9 118.7 47.9 183.8 238.0 50.9 131.3 173.0 88.9 65.4 91.2 © 2004 www.ChemReview. 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