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I need help with my ochem homework. We are currently studying amines

1 equivaient

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In pyridine moiety 'N' centre acts as a electron withdrawing group. So para NH2 group is deactivated by extended conjugation. The meta NH2 group thus attacks the carbonyl centre of the anhydride of benzoic acid and forms the subsequent amide. Now a benzoic acid is formed in the process which exchanges proton with the pyridine which is a base.

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