Exam 21: Carboxylic Acid Derivatives

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Provide the structure of o-bromobenzoyl chloride.

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Cyclic esters are called ________.

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Complete the following reaction by filling in the necessary starting material. Complete the following reaction by filling in the necessary starting material.

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Provide the major organic product in the reaction of propanoyl chloride with CH3SH.

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Provide the name of CH3O2CH2CH2CH2CH3.

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Provide the structure of γ-butyrolactam.

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Provide the name of the compound shown below. Provide the name of the compound shown below.

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What compound is produced when N,N-dimethylpropanamide is treated with LiAlH4?

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What is the predicted major product of the following reaction? What is the predicted major product of the following reaction?

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Name the compound which results when δ-valerolactone is heated in a large excess of methanol in the presence of catalytic acid.

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What is the correct IUPAC name for the following compound? What is the correct IUPAC name for the following compound?

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Propose a synthesis of PhNHCHO from benzene.

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Show how you could perform the following synthesis: Show how you could perform the following synthesis:

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The hydrolysis of esters, amides, and nitriles ________.

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While the carbonyl stretching frequency for simple aldehydes, ketones, and carboxylic acids is about 1710 cm-1, the carbonyl stretching frequency for acid chlorides is about ________.

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Provide the proper IUPAC name for the compound below. Provide the proper IUPAC name for the compound below.

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Predict the major product of the following reaction. Predict the major product of the following reaction.

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Propose a synthesis of 2-phenylethylamine from toluene and any other necessary reagents.

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What are the major organic products when 1 equivalent of acetic formic anhydride reacts with 1 equivalent of methanol?

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While the carbonyl stretching frequency for simple aldehydes, ketones, and carboxylic acids is about 1710 cm-1, the carbonyl stretching frequency for amides is about ________.

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