Increasing order of basic strength is:

aniline < methylaniline < dimethylaniline

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dimethylaniline < methylaniline < aniline

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dimethylaniline < aniline < methylaniline

No worries! We‘ve got your back. Try BYJU‘S free classes today!

aniline < dimethylaniline < methylaniline

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Solution

The correct option is A aniline < methylaniline < dimethylaniline
The basicaly order is aniline<methylaniline<dimethyaniline method group is electron donating group so,shoues +I effect and makes lone pair or nitrogen more destalrlused which then fastly gets delocalised with electrons on benzene ring so more the number of methyl groups more faster will be the delocalished or resonence.

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Convert

(i) 3-Methylaniline into 3-nitrotoluene.

(ii) Aniline into 1,3,5-tribromobenzene.

(C_{6} H_{5} N_{2}^{+} C l^{-})

C u C N / K C N

(i i) H_{2} O

(i i i) C H_{3} C H_{2} O H

(i) C_{2} H_{5} N H_{2}, C_{2} H_{5} O H, (C H_{3})_{3} N

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