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(D) The reaction proceeds as follows:$1$. Electrophilic aromatic substitution (nitration) of chlorobenzene with $Conc. \ HNO_3$ and $Conc. \ H_2SO_4$

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$4-$Nitrophenol

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(D) The reaction proceeds as follows:$1$. Electrophilic aromatic substitution (nitration) of chlorobenzene with $Conc. \ HNO_3$ and $Conc. \ H_2SO_4$ yields a mixture of $o$-nitrochlorobenzene (minor) and $p$-nitrochlorobenzene (major).$2$. Nucleophilic aromatic substitution of the major product,$p$-nitrochlorobenzene,with $NaOH$ at $443 \ K$ followed by acidification $(H_3O^+)$ replaces the $-Cl$ group with an $-OH$ group.$3$. The final major product is $p$-nitrophenol ($4$-nitrophenol).

Identify the major product of the following reaction sequence:

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