The major product of the following reaction i | vedclass

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(D) The reaction proceeds in two steps: $1$. Diazotization: The primary aromatic amine group $(-NH_2)$ reacts with $NaNO_2$ and $HCl$ at $0-5 \ ^\circ

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(D) The reaction proceeds in two steps: $1$. Diazotization: The primary aromatic amine group $(-NH_2)$ reacts with $NaNO_2$ and $HCl$ at $0-5 \ ^\circ C$ to form a diazonium salt $(-N_2^+Cl^-)$. $2$. Intramolecular Coupling: In the presence of aqueous $NaOH$,the phenolic $-OH$ group is deprotonated to form a phenoxide ion,which is a strong activating group. This phenoxide ion then undergoes an intramolecular electrophilic aromatic substitution (coupling) with the diazonium group to form a cyclic azo compound.

The major product of the following reaction is

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