Identify the product Z in the following react | vedclass

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(A) $1$. The reaction of aniline with acetyl chloride $(CH_3COCl)$ is an acetylation reaction,which protects the amino group to form $X$,which is acet

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p-Bromoaniline

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(A) $1$. The reaction of aniline with acetyl chloride $(CH_3COCl)$ is an acetylation reaction,which protects the amino group to form $X$,which is acetanilide $(C_6H_5NHCOCH_3)$.$2$. Acetanilide $(X)$ undergoes electrophilic aromatic substitution with $Br_2/AlBr_3$. The acetamido group $(-NHCOCH_3)$ is ortho/para directing. Due to steric hindrance,the para-substituted product $Y$ (p-bromoacetanilide) is the major product.$3$. Finally,the hydrolysis of $Y$ with $H_3O^+$ removes the acetyl protecting group to regenerate the amino group,yielding $Z$,which is p-bromoaniline.

Identify the product $Z$ in the following reaction sequence:
Aniline $\xrightarrow{CH_3COCl} X$ $\xrightarrow{Br_2/AlBr_3} Y$ $\xrightarrow{H_3O^+} Z$

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Identify the product $Z$ in the following reaction sequence:Aniline $\xrightarrow{CH_3COCl} X$ $\xrightarrow{Br_2/AlBr_3} Y$ $\xrightarrow{H_3O^+} Z$