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(D) $1$. In reaction $(A)$, nitration of benzanilide occurs primarily at the ortho and para positions of the aniline ring due to the activating effect

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(D) $1$. In reaction $(A)$, nitration of benzanilide occurs primarily at the ortho and para positions of the aniline ring due to the activating effect of the $-NHCOPh$ group. The product shown in the image is incorrect.$2$. In reaction $(B)$, aryl halides do not undergo nucleophilic substitution with potassium phthalimide under standard conditions, so no reaction occurs.$3$. In reaction $(C)$, the carbylamine reaction produces an isocyanide, which upon reduction with $Sn/HCl$ yields a secondary amine ($N$-methylbenzylamine), not the primary amine shown.$4$. In reaction $(D)$, the Hoffmann bromamide degradation of propanamide $(CH_3CH_2CONH_2)$ correctly yields ethylamine $(CH_3CH_2NH_2)$ along with the specified byproducts. This is a standard textbook reaction.

Consider the following reactions and identify the correct reaction.

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