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(C) conjugate acid is formed by the protonation of a base. $A$ stronger conjugate acid is formed from a weaker base.Among the given substituted anilin

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(C) conjugate acid is formed by the protonation of a base. $A$ stronger conjugate acid is formed from a weaker base.Among the given substituted anilines, the base strength depends on the electron-donating or electron-withdrawing nature of the substituents.The $-NO_2$ group in $4$-nitroaniline is a strong electron-withdrawing group via resonance and induction, which significantly reduces the availability of the lone pair on the nitrogen atom, thus making it the weakest base.Since the strength of a conjugate acid is inversely proportional to the strength of its parent base, the protonated form of $4$-nitroaniline is the strongest conjugate acid.

The strongest conjugate acid will result from:

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