In the reaction shown below,the major product | vedclass

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(A) The starting material contains both a primary aliphatic amine $(-CH_2NH_2)$ and a primary amide $(-CONH_2)$ group.Aliphatic amines are significant

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(A) The starting material contains both a primary aliphatic amine $(-CH_2NH_2)$ and a primary amide $(-CONH_2)$ group.Aliphatic amines are significantly more nucleophilic and basic than amides because the lone pair on the nitrogen of the amide is delocalized into the carbonyl group (resonance).Therefore,the reaction with acetic anhydride (an acylating agent) will selectively occur at the more nucleophilic $-CH_2NH_2$ group to form an amide.The primary amide group $(-CONH_2)$ is much less reactive towards acylation under these conditions,so the major product is the $N$-acetylated derivative of the aliphatic amine.

In the reaction shown below,the major product$(s)$ formed is/are:

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