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Q. Assertion $p$-toluidine is a stronger base than $m$-toluene.
Reason Methyl group from $m$-position exerts smaller electron donating inductive $(+I)$ effect than from $p$-position.

AIIMSAIIMS 2014

Solution:

- $CH _{3}$ group exerts greater inductive effect from $m$-position than from $p$-position. However, it is the hyperconjugation effect of $- CH _{3}$ from $p$-position which increases basic strength of $p$-isomer.