it shud be a na................ h bondin ....bt answer given is difrnt
Acetanilide on nitration followed by alkaline hydrolysis mainly gives
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8 Answers
this was a straight forward question
Direct Nitration of aniline is not possible, So this is one way of doing nitration of aniline (first converting it to acetanilide)
ya itz para............... .cuz itz more stable then ortho............ i confirmed
Q27 Acetanilide on nitration followed by alkaline hydrolysis mainly gives
a) o-nitroacetanilide
b) p-nitroaniline
c) m-nitroaniline
d) 2,4,6-trinitroaniline
Your Answer: (d)
Correct Answer: (b)
Score: -1
NH2 is highly activating, now if we convert it to NHCOCH3, the activating power is reduced to a gud extent, (to such an extent that the opo products that we get in place of NH2 is stopped at just o or p products) u can anyway not carry out nitration in presence of NH2 gp as its interaction with H+ makes it a strongly deactivating group..hence
B)
cheers!!