A) \[+R-\]effect of\[-N{{H}_{2}}\]group
B) \[-I-\]effect of\[-N{{H}_{2}}\]group
C) \[-R-\]effect of\[-N{{H}_{2}}\]group
D) Â hyperconjugation effect
Correct Answer: A
Solution :
\[-N{{H}_{2}}\]has\[+R\]effect, it donates electrons to the benzene ring. As a result, the lone pair of electrons on the N-atom get delocalized over the benzene ring and thus less readily available for protonation. Hence, aniline is a weaker base than cyclohexylamine. resonance structures of anilineYou need to login to perform this action.
You will be redirected in
3 sec