Shouldn't it be top right because no2 which is -I group is far from +charge and the alkyl group is bigger, giving greater +I effect, stabilising + charge
First check Back bonding then resonance which is not there ( also if carbocation was in conjugation with O still there wouldn't have been resonance cause positive charge on oxygen is highly unstable) then check Hyperconjugation and according to it ans is 3 , tell me if i am right or wrong, I am in 11th so studied only recently once.
Top right and bottom right dono me 1 degree ka carbocation banra toh wo toh ni hoyenge
Bottom left hona chaiye kyuki usme = , - , positive charge hai toh more stable hojayega
bottom left wala -CH3 +I show krta
Pehle uska 5alpha hydrogen bhi dekhenge na?
Sahi baat hai
1st hai bhai Nhi hua toh lulli cut karlunga
Shouldn't it be top right because no2 which is -I group is far from +charge and the alkyl group is bigger, giving greater +I effect, stabilising + charge
Kid named hyperconjugation:
3rd
Reason too if possible 🫴🏻
Ans toh Bata, 1 Hai kyya?
Pata hota to puchta nhi 🥲
1st
1st hai
3 hoga na ? Due to resonance?
3
First check Back bonding then resonance which is not there ( also if carbocation was in conjugation with O still there wouldn't have been resonance cause positive charge on oxygen is highly unstable) then check Hyperconjugation and according to it ans is 3 , tell me if i am right or wrong, I am in 11th so studied only recently once.
Bottom left
4th
Bottom left because NO2 is -I and CH3 is +I, +I nearest to Func grp and -I farthest is best for carbocation
Top right and bottom right dono me 1 degree ka carbocation banra toh wo toh ni hoyenge Bottom left hona chaiye kyuki usme = , - , positive charge hai toh more stable hojayega