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OpenStudy (anonymous):

anyone...nitration of aniline???

OpenStudy (anonymous):

the products are meta,para and ortho aniline....because the nitration of aniline involves anilinium ion which is meta directing

OpenStudy (anonymous):

In nitration you add two concentrated acids:- HNO3 and H2SO4 both strong acids. Always the acid base neutralization reactions are fastest. Even though NH2 group in aniline is a weak base , its neutraliztion with a very strong acid is still faster than nitration. Hencee if you carry the acid base reaction(Basically a protonation of the N group), you would end up with an NH3+ group attached to benzene which is deactivating. Hence the meta substitution cannot be ruled out here and you would get all products ortho, meta and para.

OpenStudy (anonymous):

which one is the major one????

OpenStudy (anonymous):

There's no clear major. I'm not too sure of the percentages but i think you get 40%para , 45% meta and 15% ortho.

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