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(C) The reaction of $p$-nitroaniline with $ICl$ is an electrophilic aromatic substitution reaction. The $-NH_2$ group is a strong activating group and

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$2,6-$diiodo$-4-$nitroaniline

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(C) The reaction of $p$-nitroaniline with $ICl$ is an electrophilic aromatic substitution reaction. The $-NH_2$ group is a strong activating group and is ortho/para directing. The $-NO_2$ group is a strong deactivating group and is meta directing. In $p$-nitroaniline,the positions ortho to the $-NH_2$ group are also meta to the $-NO_2$ group. Therefore,both ortho positions are activated by the $-NH_2$ group and directed by the $-NO_2$ group. Thus,iodination occurs at both ortho positions relative to the $-NH_2$ group,yielding $2,6$-diiodo-$4$-nitroaniline.

The major product $(x)$ in the following reaction is:

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