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Multiple Choice

In base hydrolysis of an amide, the nitrogen-containing product is which?

In base hydrolysis of an amide, the reaction splits the molecule into a carboxylate and the nitrogen-containing fragment as an amine. The hydroxide-driven mechanism cleaves the C–N bond, so the carbonyl portion becomes a carboxylate, while the nitrogen ends up as the amine (neutral, not protonated). This differs from acid hydrolysis, which gives a carboxylic acid and an ammonium salt form of the amine. Therefore, the nitrogen-containing product is an amine.

In base hydrolysis of an amide, the reaction splits the molecule into a carboxylate and the nitrogen-containing fragment as an amine. The hydroxide-driven mechanism cleaves the C–N bond, so the carbonyl portion becomes a carboxylate, while the nitrogen ends up as the amine (neutral, not protonated). This differs from acid hydrolysis, which gives a carboxylic acid and an ammonium salt form of the amine. Therefore, the nitrogen-containing product is an amine.