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A tertiary butyl carbocation is more stable than a secondary butyl carbocation because of which of the following?
A
$+R$ effect of $-CH_3$ groups
B
$-R$ effect of $-CH_3$ groups
C
Hyperconjugation
D
$-I$ effect of $-CH_3$ groups
Detailed Solution
Tertiary butyl carbocation has 9 $\alpha$-H atoms, while secondary butyl carbocation has 5 $\alpha$-H atoms.
The more the number of $\alpha$-H atoms, the greater the hyperconjugation, and hence the greater the stability of the carbocation.
