Which of the following compounds on hydrolysi | vedclass

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(B) The reaction sequence is a Hoffmann bromamide degradation,which converts an amide to an amine with one less carbon atom. The final product is $2-a

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(B) The reaction sequence is a Hoffmann bromamide degradation,which converts an amide to an amine with one less carbon atom. The final product is $2-aminophenol$. The amide precursor is $2-hydroxybenzamide$. This amide is formed from $2-hydroxybenzoic$ acid (salicylic acid) via $SOCl_2$ and $NH_3$. The reactant $(A)$ is $2-hydroxybenzoic$ acid. Among the options,hydrolysis of the ester in option $(B)$ (which is $2-nitrophenyl-2-hydroxybenzoate$ or similar derivative) yields the required acid. Specifically,the structure in option $(B)$ represents an ester that upon hydrolysis yields $2-hydroxybenzoic$ acid and $2-nitrophenol$.

Which of the following compounds on hydrolysis gives reactant $(A)$?

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