Exam 21: Carboxylic Acid Derivatives
Exam 1: Structure and Bonding127 Questions
Exam 2: Acids and Bases; Functional Groups136 Questions
Exam 3: Structure and Stereochemistry of Alkanes134 Questions
Exam 4: The Study of Chemical Reactions128 Questions
Exam 5: Stereochemistry132 Questions
Exam 6: Alkyl Halides; Nucleophilic Substitution137 Questions
Exam 7: Structure and Synthesis of Alkenes; Elimination131 Questions
Exam 8: Reactions of Alkenes134 Questions
Exam 10: Structure and Synthesis of Alcohols136 Questions
Exam 11: Reactions of Alcohols125 Questions
Exam 12: Infrared Spectroscopy and Mass Spectrometry121 Questions
Exam 13: Nuclear Magnetic Resonance Spectroscopy130 Questions
Exam 14: Ethers, Epoxides, and Thioethers127 Questions
Exam 15: Conjugated Systems, Orbital Symmetry, and Ultraviolet Spectroscopy130 Questions
Exam 16: Aromatic Compounds128 Questions
Exam 17: Reactions of Aromatic Compounds129 Questions
Exam 18: Ketones and Aldehydes131 Questions
Exam 19: Amines127 Questions
Exam 20: Carboxylic Acids125 Questions
Exam 21: Carboxylic Acid Derivatives130 Questions
Exam 22: Condensations and Alpha Substitutions of Carboxyl Compounds127 Questions
Exam 23: Carbohydrates and Nucleic Acids126 Questions
Exam 24: Amino Acids, Peptides, and Proteins127 Questions
Exam 25: Lipids127 Questions
Exam 26: Synthetic Polymers128 Questions
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Phthalic acid produces what acid derivative upon heating?
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Correct Answer:
D
Provide the major organic product in the reaction shown below. 

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Propose a synthesis of benzonitrile from benzene and any other necessary reagents.
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1) HNO3, H2SO4
2) Fe, HCl
3) NaNO2, HCl, cold
4) CuCN
Which of the following structures are carboxylic acid derivatives? 

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Why are β-lactams, such as penicillins and cephalosporins, unusually reactive amides?
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Provide an arrow pushing mechanism for the following reaction. Show all intermediate structures and formal charges. You do not need to show resonance structures. 

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Two equivalents of methyl magnesium bromide will add to ________.
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Show how one might synthesize phenylacetone using toluene, NaCN, and any other necessary reagents.
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Describe, in short phrases, the three step mechanism by which hexanoyl chloride reacts with dimethylamine.
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Which of the following compounds is(are) hydrolyzed to butanoic acid upon heating in 

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