Identify product B in the following reaction: | vedclass

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(A) $1$. The reaction of acetanilide with a nitrating mixture $(conc. HNO_3 + conc. H_2SO_4)$ leads to electrophilic aromatic substitution,primarily y

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$p$-nitroaniline

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(A) $1$. The reaction of acetanilide with a nitrating mixture $(conc. HNO_3 + conc. H_2SO_4)$ leads to electrophilic aromatic substitution,primarily yielding $p$-nitroacetanilide as product $A$ due to the steric hindrance at the ortho position.$2$. The subsequent step involves the hydrolysis of the amide group $(-NHCOCH_3)$ in $p$-nitroacetanilide using acid $(H^+)$ or base $(OH^-)$.$3$. This hydrolysis converts the $-NHCOCH_3$ group back into an amino group $(-NH_2)$,resulting in the formation of $p$-nitroaniline as product $B$.

Identify product $B$ in the following reaction:
Acetanilide $\xrightarrow[conc. H_2SO_4]{conc. HNO_3}$ $A$ $\xrightarrow{H^+ \text{ or } OH^-}$ $B$

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Identify product $B$ in the following reaction:Acetanilide $\xrightarrow[conc. H_2SO_4]{conc. HNO_3}$ $A$ $\xrightarrow{H^+ \text{ or } OH^-}$ $B$