Exam 20: Carboxylic Acids and Their Derivatives

Predict the product for the following reaction.

(Essay)

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Question 141

Provide the structure for (3S,4S)-3-hydroxy-4-phenylnonanoic acid.

(Essay)

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Question 142

Propose a stepwise synthesis for 2-phenylethanoyl chloride, using toluene and/or carbon dioxide as your only source of carbon and any other reagents necessary.

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Question 143

Rank the following acids in decreasing (strongest to weakest) order of acidity.

(Multiple Choice)

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Question 144

Showing 141 - 144 of 144

Predict the product for the following reaction.

Provide the structure for (3S,4S)-3-hydroxy-4-phenylnonanoic acid.

Propose a stepwise synthesis for 2-phenylethanoyl chloride, using toluene and/or carbon dioxide as your only source of carbon and any other reagents necessary.

Rank the following acids in decreasing (strongest to weakest) order of acidity.

A Review of General Chemistry: Electrons, Bonds, and Molecular Properties

Molecular Representations

Acids and Bases

Alkanes and Cycloalkanes

Stereoisomerism

Chemical Reactivity and Mechanisms

Alkyl Halides: Nucleophilic Substitution and Elimination Reactions

Addition Reactions of Alkenes

Alkynes

Radical Reactions

Synthesis

Alcohols and Phenols

Ethers and Epoxides; Thiols and Sulfides

Infrared Spectroscopy and Mass Spectrometry

Nuclear Magnetic Resonance Spectroscopy

Conjugated Pi Systems and Pericyclic Reactions

Aromatic Compounds

Aromatic Substitution Reactions

Aldehydes and Ketones

Alpha Carbon Chemistry: Enols and Enolates

Amines

Introduction to Organometallic Compounds

Carbohydrates

Amino Acids, Peptides, and Proteins

Lipids

Synthetic Polymers

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