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1 3 Unit II - Equilibrium - Chapter 13 2.1. Characterize chemical reactions in terms of reversibility and relative concentrations of reactants and products. [Readings 13.1 Problems 18] Demonstration: 4 Demonstration: 5 Fe+3 + SCN- --> FeSCN+2 Fe+3 + SCN- --> FeSCN+2 Fe+3 + SCN- --> FeSCN+2 2 6 7 The relative amounts of reactants and products in a chemical reaction are effected by concentration changes. 8 9 10 Fe+3 + SCN- --> FeSCN+2 Fe+3 + SCN- --> FeSCN+2 Fe+3 + SCN- --> FeSCN+2 All reactants and products are present during the reaction. 11 Observations on the chemical reaction: Fe+3 + SCN- --> FeSCN+2 All reactants and products are present during the reaction. Reactions are reversible. The relative amounts of reactants and products in a chemical reaction are effected by concentration changes. 12 AgNO3(aq) + NaC2H3O2(aq) --> AgC2H3O2(s)+ NaNO3(aq) Ag+ + NO3- + Na+ + C2H3O2- --> AgC2H3O2(s) + Na+ + NO3Net Ionic Equation Ag+(aq) + C2H3O2-(aq) --> AgC2H3O2(s) 13 Ag+ + C2H3O2- --> AgC2H3O2(s) Initial .002 moles .002 moles Final (expected) 0 moles 0 moles Final (experimental) 0 moles .002 moles .122 g = .000730 moles Where did the rest go? .00127 moles .00127 moles .000730 moles 14 AgC2H3O2(s) -->Ag+ + C2H3O2Initial .002 moles 0 moles 0 moles Page 1 Final .000730 moles .00127 moles .00127 moles ---------------------------------------------------------------------------------- 15 16 Initial .02 moles Final .01873 moles 0 moles 0 moles .00127 moles .00127 moles AgC2H3O2(s) <==> Ag+(aq) + C2H3O2-(aq) AgC2H3O2(s) <==> Ag+(aq) + C2H3O2-(aq) 17 18 19 20 [Ag+] vs. [C2H3O2- ] 21 2.2. Determine equilibrium expressions for homogeneous and heterogeneous chemical reactions from stoichiometry. [Readings 13.2, 13.3, & 13.4 Problems 1, 2, 26, 28, 34, 36, 38, & 46] aA + bB <==> cC + dD 22 [Ag+] vs. [C2H3O2-] ---------- [Ag+] vs. 1/[ C2H3O2 -] [Ag+] vs. [C2H3O2-] ---------- [Ag+] vs. 1/[ C2H3O2 -] [Ag+] vs. [C2H3O2-] ---------- [Ag+] vs. 1/[ C2H3O2 -] In heterogeneous equilibria, pure liquids or solids are not included. In aqueous equilibria, pure water is not included. 23 Superscripts? A + B <==> 2C A + B <==> C + C K = [C] [C] / [A] [B] K = [C]2 / [A] [B] 24 Example • Reaction N2 (g) + 3 H2 (g) –––> 2 NH 3 (g) 25 Example • Reaction N2 (g) + 3 H2 (g) –––> 2 NH 3 (g) K=? 26 Example • Reaction N2 (g) + 3 H2 (g) –––> 2 NH 3 (g) 27 Example • Reaction N2 (g) + 3 H2 (g) –––> 2 NH 3 (g) Page 2 For rxn: 2 NH3 (g) –––> N2 (g) + 3 H2 (g) K’ = ? 28 Example • Reaction N2 (g) + 3 H2 (g) –––> 2 NH 3 (g) For rxn: 2 NH3 (g) –––> N2 (g) + 3 H2 (g) K’ = 1/K 29 Pure solids or liquids? What is the [AgC2H3O2] ? = moles / Liter {moles = weight / MW} = weight / Lx MW = density / MW = constant for pure substance 30 Water not included? What is the concentration of water in pure water? 1000g / L (1 mole / 18 g) = 55.6 M What is the concentration of water in 0.1 M NaCl solution? (5.9 g) 994g / L (1 mole / 18 g) = 55.2 M Therefore [H2O] in solutions is a constant. 31 aA + bB <==> cC + dD In heterogeneous equilibria, pure liquids or solids are not included. In aqueous equilibria, pure water is not included. 32 Example Write equilibruim expressions for the following reactions: (in a 1 liter container) A. 1/8 S8 (s) + O2 (g) –––> SO2 (g) B. NH3 (aq) + H2O (l) –––> NH 4+ (aq) + OH- (aq) 33 Gas Phase Reactions Often partial pressures are used instead of concentrations for gas phase reactions. Rxn: N2O4 (g) –––2 NO2 (g) What is the eauilibrium constant? Solve for Kp 34 Gas Phase Reactions Often partial pressures are used instead of concentrations for gas phase reactions. Rxn: Page 3 N2O4 (g) –––2 NO2 (g) What is the eauilibrium constant? Solve for Kp 35 36 37 38 K is temperature dependent: K Values for Related Chemical Equations (1) A <=> B K1= x (2) B <=> A K2= K1-1 = x-1 (1) A <=> B K1= x (3) 2A <=> 2B K3= K12 = x2 2.3. Determine the stoichiometric relationship between initial and equilibrium concentrations of reactants and products. [Readings 13.5 Problems] 2.4. Determine values for K from equilibrium concentrations of reactants and products in a chemical reaction. [Readings 13.5 Problems 80, ] H2O + HC7H5O2 <=> H3O+ + C7H5O2Initial Equilibrium Change Equilibrium 0.10 M 0M 0M ? 2.57 x 10-3 ? -2.57 x 10-3 9.74 x 10-2 +2.57 x 10-3 +2.57 x 10-3 2.57 x 10-3 2.57 x 10-3 Initial ----- amount based on experiment Change ----- amount based on stoichiometry Equilibrium ----- amount based on equilibrium 39 2.5. Determine the equilibrium concentrations of reactants and products of a chemical reaction from initial concentrations and values of K. [Readings 13.5 Problems 10, 11, 25, 48, 52, 54, 56, & 58] 40 H2O + HC7H5O2 <=> H3O+ + C7H5O2If 61 g of HC7H5O2 is dissolved in 1 L of solution, what is [H3O+] at equilibrium? Kc = 6.3x10-5 41 42 2.6. Determine if equilibrium has been reached in a chemical reaction; determine the direction the reaction will shift if equilibrium has not been reached. [Readings 13.5 Problems ex 13.6 & prob. 13.7] rR <==> pP Page 4 K = [P]ep / [R]er 43 44 45 46 Q = [P]ip / [R]ir 2.7. Use Le Châtelier’s Principle to predict the direction a reaction at equilibrium will shift as a result of changes in concentration, pressure/volume, and temperature as it approaches a new equilibrium. [Readings 13.6, 13.7, 13.8, & 13.9 Problems 66, 68, 70, & 72] Le Châtelier’s Principle If a stress is put on a system in equilibrium, it will shift (adjust) to minimize (offset, reverse) the effect of the stress. Le Châtelier’s Principle If a stress is put on a system in equilibrium, it will shift (adjust) to minimize (offset, reverse) the effect of the stress. Equilibrium: A system is at equilibrium when the rate of the forward reaction is equal to the rate of the reverse reaction. This does not mean: The amounts are equal The reaction has stopped 47 48 49 50 A <==> B Stress -- changes that effect rates of forward and reverse reactions differently concentration temperature catalyst? pressure? Shift -- An adjustment in the concentrations of reactants and products Shift to right -- increase [P], decrease [R] Shift to left -- increase [R], decrease [P] Minimize A(g) + B(g) <=> 2C(g) I 2 5 0 C -1 -1 +2 K = [C]2 / [A] [B] Page 5 E add 19 A C new E 51 52 53 54 1 4 2 K=1 20 4 2 Q -2 -2 +4 18 2 6 1 K=1 N2 + 3 H2 <==> 2 NH3 N2 + 3 H2 <==> 2 NH3 Demo: 2 NO(g) + O2(g) --> 2 NO2(g) Initial 20 mL 10 mL Predicted 20 mL Actual 15 mL 2 NO2(g) <==> N2O4(g) + brown colorless Change Temperature 2 NO2(g) <==> N2O4(g) + Increase T -- More Heat -- P constant Equilibrium Shifts to Reduce Heat Color Deepens K = [N2O4] / [NO2]2 , K decreases 55 Therefore K is T dependent Change Pressure (by decreasing V) 2 NO2(g) <==> N2O4(g) + 56 PT Kp Equilibrium 20 atm 20 atm 40 atm .05 P x 2 (1/2 V) 40 atm 40 atm 80 atm .025 Change -10 atm +5 atm New 30 atm Equilibrium 45 atm 75 atm .05 Self Test X(g) + H2O(l) <==> Q (s) + Y(g) Change increase Px increase [Y] remove 1/2 Q increase PT increase T Shift H = +150 kJ Change in K Page 6 catalyst Page 7