Identify the product Z in the following react | vedclass

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(A) Step $1$: Aniline $(C_6H_5NH_2)$ reacts with acetic anhydride $((Ac)_2O)$ to form acetanilide $(X = C_6H_5NHCOCH_3)$.Step $2$: Acetanilide undergo

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$p-$Bromoaniline

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(A) Step $1$: Aniline $(C_6H_5NH_2)$ reacts with acetic anhydride $((Ac)_2O)$ to form acetanilide $(X = C_6H_5NHCOCH_3)$.Step $2$: Acetanilide undergoes electrophilic aromatic substitution with $Br_2/CCl_4$ to form $p-$bromoacetanilide $(Y = Br-C_6H_4-NHCOCH_3)$ as the major product due to the steric hindrance at the ortho position.Step $3$: Hydrolysis $(HOH)$ of $p-$bromoacetanilide removes the acetyl group to yield $p-$bromoaniline $(Z = Br-C_6H_4-NH_2)$.

Identify the product $Z$ in the following reaction:
$C_6H_5NH_2$ $\xrightarrow{(Ac)_2O} X$ $\xrightarrow{Br_2/CCl_4} Y$ $\xrightarrow{HOH} Z$

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Identify the product $Z$ in the following reaction:$C_6H_5NH_2$ $\xrightarrow{(Ac)_2O} X$ $\xrightarrow{Br_2/CCl_4} Y$ $\xrightarrow{HOH} Z$