Stability of Carbocation
how is the meta one most stable , i was expecting ortho or para one to be most stable
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@Dexter
Note for OP
+solved @user1 @user2... to close the thread when your doubt is solved. Mention the users who helped you solve the doubt. This will be added to their stats.ig cuz usme Nitrogen ke bonded pair se resonance ho raha
thats why
and see
in the other ones bhi
thats exactly the reason o/p should be it
N se resonance hoga but
NH2 is O/P Directing for Electrophieles
in those cases 2 pi bonds will be directly adjacent
it creates -Ve charge at O/P
which will stablise +Ve
yes it will however agar wo resonance kaise karega wo bhi dekho
then meta one is the most stable here cuz baaki jagah
the lp on N is unable to participate in resonance
in 1 and 4 it doe
in III the lp does get to delocalise
does
wait
nvm
i get it
Yes but it wont cuz adjacent me pi bonds benzene me nahi aana chahte
+solved @Phalawor
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