What will be the structure of product T in th | vedclass

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(D) The reaction proceeds in two steps: $1$. The first step is the Hofmann bromamide degradation reaction,where the amide $p-CH_3-C_6H_4-CONH_2$ react

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(D) The reaction proceeds in two steps: $1$. The first step is the Hofmann bromamide degradation reaction,where the amide $p-CH_3-C_6H_4-CONH_2$ reacts with $NaOH/Br_2$ to form the primary amine $p-CH_3-C_6H_4-NH_2$ ($p$-toluidine). $2$. The second step is the acylation of the amine with benzoyl chloride $(C_6H_5COCl)$. The lone pair on the nitrogen atom of the amine attacks the carbonyl carbon of the benzoyl chloride,leading to the formation of an amide: $p-CH_3-C_6H_4-NH-CO-C_6H_5$ ($N$-(p-tolyl)benzamide). Comparing this with the given options,option $D$ represents the correct structure.

What will be the structure of product $T$ in the following reaction?

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