L-13
... whereas no reaction took place by other representative Lewis acids such as AlCl3 and BF3. Introduction Nucleophilic substitution of the hydroxy group in alcohols intrinsically requires an equimolar (or greater) amount of acid because of the poor leaving ability of the OH group. To avoid the use of e ...
... whereas no reaction took place by other representative Lewis acids such as AlCl3 and BF3. Introduction Nucleophilic substitution of the hydroxy group in alcohols intrinsically requires an equimolar (or greater) amount of acid because of the poor leaving ability of the OH group. To avoid the use of e ...
CHM_221_201620 - Oakton Community College
... 1. Apply the three models of bonding–Lewis, valence bond and molecular orbital theory–as well as their extensions–hybridization and resonance–to describe covalent bonding in organic species. 2. Draw and interconvert drawings of neutral and charged organic species using condensed formulae, bond-line ...
... 1. Apply the three models of bonding–Lewis, valence bond and molecular orbital theory–as well as their extensions–hybridization and resonance–to describe covalent bonding in organic species. 2. Draw and interconvert drawings of neutral and charged organic species using condensed formulae, bond-line ...
CHM_223_201620 - Oakton Community College
... 1. Apply the three models of bonding–Lewis, valence bond and molecular orbital theory–as well as their extensions–hybridization and resonance–to describe covalent bonding in organic species. 2. Draw and interconvert drawings of neutral and charged organic species using condensed formulae, bond-line ...
... 1. Apply the three models of bonding–Lewis, valence bond and molecular orbital theory–as well as their extensions–hybridization and resonance–to describe covalent bonding in organic species. 2. Draw and interconvert drawings of neutral and charged organic species using condensed formulae, bond-line ...
Organic Unit - hrsbstaff.ednet.ns.ca
... 1. Why does oxygen have to bond twice in a molecule? 2. How many times would these atoms bond? a) S b) Cl c) N d) F e) P 3. Which families cannot be made from methane? 4. Do any groups have the same general formula? b) Two Physical Properties - The presence of a functional group has a major effect o ...
... 1. Why does oxygen have to bond twice in a molecule? 2. How many times would these atoms bond? a) S b) Cl c) N d) F e) P 3. Which families cannot be made from methane? 4. Do any groups have the same general formula? b) Two Physical Properties - The presence of a functional group has a major effect o ...
powerpoint
... takes place when an acid and base react with each other. The H+ ion in the acid reacts with the OH- ion in the base, causing the formation of water. Product of this reaction is typically an ionic salt and water: HA + BOH ---> H2O + BA ...
... takes place when an acid and base react with each other. The H+ ion in the acid reacts with the OH- ion in the base, causing the formation of water. Product of this reaction is typically an ionic salt and water: HA + BOH ---> H2O + BA ...
Chapter one: Unsaturated Hydrocarbons
... c. Carbon dioxide and water d. Carbon and water 6. What is the difference between a. Cyclic an acyclic hydrocarbon? Cyclic: it has rings of carbon atoms or it contains closed chain Acyclic: it has no rings of carbon atoms. Or it contains open chain b. continuous- chain alkane and branched-chain alka ...
... c. Carbon dioxide and water d. Carbon and water 6. What is the difference between a. Cyclic an acyclic hydrocarbon? Cyclic: it has rings of carbon atoms or it contains closed chain Acyclic: it has no rings of carbon atoms. Or it contains open chain b. continuous- chain alkane and branched-chain alka ...
Carbon Chemistry
... gases at room temperature and are called: • methane, CH4 • ethane, C2H6 • propane, C3H8 • butane, C4H10 ...
... gases at room temperature and are called: • methane, CH4 • ethane, C2H6 • propane, C3H8 • butane, C4H10 ...
Chapter 10 The Chemistry of Alcohols and Thiols
... Eq. 10.26 of the text shows that the nucleophilic reaction of the bromide ion on the reactive intermediate occurs by a concerted (SN2) substitution reaction. Therefore, the reaction should occur with inversion of stereochemistry, and the product would then be (S)-2-bromopentane. The SN2 reaction occ ...
... Eq. 10.26 of the text shows that the nucleophilic reaction of the bromide ion on the reactive intermediate occurs by a concerted (SN2) substitution reaction. Therefore, the reaction should occur with inversion of stereochemistry, and the product would then be (S)-2-bromopentane. The SN2 reaction occ ...
Chem 231 Exam #3 Study Guide
... Know the order of substrate reactivities for the different reactions Know how to predict nucleophilicity (two rules) and the relative order of nucleophiles in protic solvent Be able to predict a good versus bad leaving group Know how solvents effect SN1 versus SN2 reactions Know how to name alkenes ...
... Know the order of substrate reactivities for the different reactions Know how to predict nucleophilicity (two rules) and the relative order of nucleophiles in protic solvent Be able to predict a good versus bad leaving group Know how solvents effect SN1 versus SN2 reactions Know how to name alkenes ...
organic chemistry ii
... Chapter 22: Carboxylic Acids and their Derivatives –Nucleophilic Acyl Substitution The common features of these classes of compounds is that they can all be hydrolyzed into carboxylic acids Syntheses of Carboxylic Acids: (i) Oxidation of aldehydes and 1o alcohols (remember 1o alcohols will only oxid ...
... Chapter 22: Carboxylic Acids and their Derivatives –Nucleophilic Acyl Substitution The common features of these classes of compounds is that they can all be hydrolyzed into carboxylic acids Syntheses of Carboxylic Acids: (i) Oxidation of aldehydes and 1o alcohols (remember 1o alcohols will only oxid ...
Organic h/w KEY - mvhs
... 2. Chain is numbered so that the C atoms of the double bond get the lowest possible numbers. Ex: CH2=CH-CH2=CH3 1-butene Alkynes: contain one or more C-C triple covalent bonds. Practice: 1. How many H atoms in Ethane, Ethene, Ethyne ...
... 2. Chain is numbered so that the C atoms of the double bond get the lowest possible numbers. Ex: CH2=CH-CH2=CH3 1-butene Alkynes: contain one or more C-C triple covalent bonds. Practice: 1. How many H atoms in Ethane, Ethene, Ethyne ...
Week 6 Solutions - Brown University Wiki
... Also note that the carbon that is labeled 1 in the first compound (note that they are the same as the molecule is symmetric) must have been the one to attack the carbon currently labeled a to make a 5 membered ring. If it is attacking carbon a – we know that the other branched carbon has to correspo ...
... Also note that the carbon that is labeled 1 in the first compound (note that they are the same as the molecule is symmetric) must have been the one to attack the carbon currently labeled a to make a 5 membered ring. If it is attacking carbon a – we know that the other branched carbon has to correspo ...
ALKANOLS (ALCOHOLS)
... Alcohols are classified as primary, secondary or tertiary, depending upon the number of alkyl groups attached to the carbon atom to which the OH group is bonded (or the number of hydrogen atoms attached to the alkanol carbon). Methanol is considered to be a primary alcohol. Primary alcohols have a ‘ ...
... Alcohols are classified as primary, secondary or tertiary, depending upon the number of alkyl groups attached to the carbon atom to which the OH group is bonded (or the number of hydrogen atoms attached to the alkanol carbon). Methanol is considered to be a primary alcohol. Primary alcohols have a ‘ ...
Chapter 15
... • Allylic and benzylc halides are classified in the same way as other halides, just add the allylic or benzylic • Tertiary allylic and benzylic halides still only undergo Sn1 reactions due to the steric hinderance. • The difference is with the primary allylic and benzylic halides. • Because they wou ...
... • Allylic and benzylc halides are classified in the same way as other halides, just add the allylic or benzylic • Tertiary allylic and benzylic halides still only undergo Sn1 reactions due to the steric hinderance. • The difference is with the primary allylic and benzylic halides. • Because they wou ...
Introduction to Organic Chemistry
... • Living things are composed of organic molecules, which means that they contain carbon – carbon has four electrons in outer shell which can bond with other atoms – carbon can be linked to other carbons or atoms such as hydrogen (H), oxygen (O) and nitrogen(N) – long links of these carbons can form ...
... • Living things are composed of organic molecules, which means that they contain carbon – carbon has four electrons in outer shell which can bond with other atoms – carbon can be linked to other carbons or atoms such as hydrogen (H), oxygen (O) and nitrogen(N) – long links of these carbons can form ...
Types of Chemical Reactions
... (Less-active metals react with steam to form a metal oxide and hydrogen gas) ...
... (Less-active metals react with steam to form a metal oxide and hydrogen gas) ...
AP Biology Functional Groups of Carbon
... between molecules. (See module on energetics) – DNA and RNA have backbones made of phosphates alternating with a deoxyribose or ribose monosaccharide. – Molecules that accept Hydrogen such as NAD+ or FAD+ contain phosphates. ...
... between molecules. (See module on energetics) – DNA and RNA have backbones made of phosphates alternating with a deoxyribose or ribose monosaccharide. – Molecules that accept Hydrogen such as NAD+ or FAD+ contain phosphates. ...
EXPERIMENT 4 Objectives Principles
... of electrons, or ions with a negative charge. They can form bond by donating electrons to another molecule having a position of lower electron density (electrophiles). Examples of nucleophilic species are: water, amine, ammonia, cyanide ion, alkoxide ion, and hydroxide ion. Alkyl halides can react w ...
... of electrons, or ions with a negative charge. They can form bond by donating electrons to another molecule having a position of lower electron density (electrophiles). Examples of nucleophilic species are: water, amine, ammonia, cyanide ion, alkoxide ion, and hydroxide ion. Alkyl halides can react w ...
-1- GLOSSARY OF CHEM 1110 ORGANIC CHEMISTRY TERMS
... homologous series: compounds which differ only by the number of CH2 units present; CH3CH2Cl, CH3CH2CH2Cl, and CH3CH2CH2CH2Cl, all belong to the same homologous series (1° alkyl chlorides). hydration: the addition of a molecule of water to the carbon-carbon double bond of an alkene to form an alcohol ...
... homologous series: compounds which differ only by the number of CH2 units present; CH3CH2Cl, CH3CH2CH2Cl, and CH3CH2CH2CH2Cl, all belong to the same homologous series (1° alkyl chlorides). hydration: the addition of a molecule of water to the carbon-carbon double bond of an alkene to form an alcohol ...
File
... ie for an alkane: CnH2n+2, (iv) structural formula as the minimal detail that shows the arrangement of atoms in a molecule, eg for butane: CH3CH2CH2CH3 or CH3(CH2)2CH3, (v) displayed formula as the relative positioning of atoms and the bonds between them (vi) skeletal formula as the simplified organ ...
... ie for an alkane: CnH2n+2, (iv) structural formula as the minimal detail that shows the arrangement of atoms in a molecule, eg for butane: CH3CH2CH2CH3 or CH3(CH2)2CH3, (v) displayed formula as the relative positioning of atoms and the bonds between them (vi) skeletal formula as the simplified organ ...
1 - vnhsteachers
... 1. Two atoms share four electrons. What type of bond exists between the two atoms? 1A. Double 2. __________ show the actual number and kinds of atoms in a molecule. 2A. Molecular formulas 3. Hydrocarbons that contain triple bonds are called: 3A. alkynes 4. Several molecules with the same composition ...
... 1. Two atoms share four electrons. What type of bond exists between the two atoms? 1A. Double 2. __________ show the actual number and kinds of atoms in a molecule. 2A. Molecular formulas 3. Hydrocarbons that contain triple bonds are called: 3A. alkynes 4. Several molecules with the same composition ...
Functional Groups III
... The carbon-halogen bonds are polar, because the electron pair is pulled closer to the halogen atom then the carbon. ...
... The carbon-halogen bonds are polar, because the electron pair is pulled closer to the halogen atom then the carbon. ...
Lesson 3 Mechanisms of Organic Reactions
... general formula R-X, where X is an electron-withdrawing group. Nucleophiles are often, though not always, negatively charged. The most widely known nucleophiles are a hydroxide ion, alkoxide ions (RO-), thiolate ions (RS-), halide ions, a hydride ion (H-), carbanions (particles with negatively charg ...
... general formula R-X, where X is an electron-withdrawing group. Nucleophiles are often, though not always, negatively charged. The most widely known nucleophiles are a hydroxide ion, alkoxide ions (RO-), thiolate ions (RS-), halide ions, a hydride ion (H-), carbanions (particles with negatively charg ...
Haloalkane
The haloalkanes (also known, as halogenoalkanes or alkyl halides) are a group of chemical compounds derived from alkanes containing one or more halogens. They are a subset of the general class of halocarbons, although the distinction is not often made. Haloalkanes are widely used commercially and, consequently, are known under many chemical and commercial names. They are used as flame retardants, fire extinguishants, refrigerants, propellants, solvents, and pharmaceuticals. Subsequent to the widespread use in commerce, many halocarbons have also been shown to be serious pollutants and toxins. For example, the chlorofluorocarbons have been shown to lead to ozone depletion. Methyl bromide is a controversial fumigant. Only haloalkanes which contain chlorine, bromine, and iodine are a threat to the ozone layer, but fluorinated volatile haloalkanes in theory may have activity as greenhouse gases. Methyl iodide, a naturally occurring substance, however, does not have ozone-depleting properties and the United States Environmental Protection Agency has designated the compound a non-ozone layer depleter. For more information, see Halomethane. Haloalkane or alkyl halides are the compounds which have the general formula ″RX″ where R is an alkyl or substituted alkyl group and X is a halogen (F, Cl, Br, I).Haloalkanes have been known for centuries. Chloroethane was produced synthetically in the 15th century. The systematic synthesis of such compounds developed in the 19th century in step with the development of organic chemistry and the understanding of the structure of alkanes. Methods were developed for the selective formation of C-halogen bonds. Especially versatile methods included the addition of halogens to alkenes, hydrohalogenation of alkenes, and the conversion of alcohols to alkyl halides. These methods are so reliable and so easily implemented that haloalkanes became cheaply available for use in industrial chemistry because the halide could be further replaced by other functional groups.While most haloalkanes are human-produced, non-artificial-source haloalkanes do occur on Earth, mostly through enzyme-mediated synthesis by bacteria, fungi, and especially sea macroalgae (seaweeds). More than 1600 halogenated organics have been identified, with bromoalkanes being the most common haloalkanes. Brominated organics in biology range from biologically produced methyl bromide to non-alkane aromatics and unsaturates (indoles, terpenes, acetogenins, and phenols). Halogenated alkanes in land plants are more rare, but do occur, as for example the fluoroacetate produced as a toxin by at least 40 species of known plants. Specific dehalogenase enzymes in bacteria which remove halogens from haloalkanes, are also known.