A series of alkyl groups CH3-, CD3, CT3 on benzene ring represents
see full answer
High-Paying Jobs That Even AI Can’t Replace — Through JEE/NEET
🎯 Hear from the experts why preparing for JEE/NEET today sets you up for future-proof, high-income careers tomorrow.
An Intiative by Sri Chaitanya
a
Increasing hyperconjugation from left to right
b
Decreasing hyperconjugation from left to right
c
Decreasing inductive effect L to R
d
All of these
answer is B.
(Unlock A.I Detailed Solution for FREE)
Best Courses for You
JEE
NEET
Foundation JEE
Foundation NEET
CBSE
Detailed Solution
(1) As atomic mass of isotopes of Hydrogen increases, [H1, D2, T3] bond vibration decreases (C – H > C –D > C-T)i.e., vibrational frequency increases, and hence bond dissociation energy increases,hence the delocalisation of α – C – H σ-bond with benzene π-bond decreases, Therefore Hyperconjugation effect decreases. That is electron donation effect by Hyper Conjugation decreases.As bond length decreases, electron density over the bond increases, hence electron density around the carbon increases, electronegativity of carbon is greater than that of Hydrogen, electron density at the carbon increases. Hence, electron donatin to the benzene ring increases, ie., I.E. strength increases.