Question Detail

CHM 102 Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions Objective Question
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Question

Which reagent reduces an amide to an amine without affecting other functional groups?
Options
A NaBH4
B LiAlH4
Correct Answer
C H2/Pd
D DIBAL-H
Correct Answer

Option B is the correct answer.

Detailed Explanation

LiAlH4 reduces amides to amines (RCONR'2 → RCH2NR'2). NaBH4 does not reduce amides under normal conditions.

Hint

Strong reducing agent.

Question Info

Course: CHM 102
Topic: Carboxylic Acid Derivatives: Nomenclature, Synthesis, and Reactions
Type: Objective
Difficulty: Not specified
Question 337 of 1999
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