For the given reaction,identify the major pro | vedclass

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(C) The reaction sequence is as follows:$1$. Benzene reacts with $Cl_2$ in the presence of $FeCl_3$ (electrophilic aromatic substitution) to form chlo

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$4-$Nitrophenol

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(C) The reaction sequence is as follows:$1$. Benzene reacts with $Cl_2$ in the presence of $FeCl_3$ (electrophilic aromatic substitution) to form chlorobenzene $(A)$.$2$. Chlorobenzene $(A)$ undergoes nitration with $Conc. HNO_3 + Conc. H_2SO_4$ to form a mixture of $o$-nitrochlorobenzene and $p$-nitrochlorobenzene. The major product is $p$-nitrochlorobenzene $(B)$ due to less steric hindrance.$3$. $p$-Nitrochlorobenzene $(B)$ undergoes nucleophilic aromatic substitution with $NaOH$ at $443 \ K$ followed by acidification $(H^+)$ to replace the $Cl$ atom with an $-OH$ group,yielding $p$-nitrophenol $(C)$.

For the given reaction,identify the major product $C$.

Similar Questions

The increasing order of nitration of the following compounds is:
$(A)$ Aniline
$(B)$ Chlorobenzene
$(C)$ Anisole
$(D)$ Toluene

The presence of the chlorine atom on the benzene ring makes the second substituent enter at which position?

Which one of the following compounds is most reactive for $ArS_N2$ reaction?

Assertion : Cyanide $(CN^{-})$ is a strong nucleophile.
Reason : Benzonitrile is prepared by the reaction of chlorobenzene with potassium cyanide.

Although chlorobenzene does not undergo the Ullmann reaction,the presence of which group at the $o-$ and $p-$ positions of chlorobenzene makes it possible to undergo the Ullmann reaction?

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