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Nitration of aniline in strong acidic medium also gives m - nitroaniline because

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inspite of substituents nitro group always goes to only m -position
in electrophilic substitution reactions amino group is meta directive
in absence of substituents nitro group always goes to m -position
in acidic (strong) medium aniline is present as anilinium ion.

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detailed solution

Correct option is D

The reason for formation of an unexpected amount of m -nitroaniline is that under strongly acidic condition of nitration, most of the aniline is converted into anilinium ion and since, -N+H3 .Due to strong -I effect,very little ortho product(2%) and   a large amount of m -nitroaniline(47%) and para nitro aniline (51%) are  obtained.

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Which of the following product is formed in the given reaction?

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