'Stability of carbocations depends upon the electron releasing inductive effect of groups adjacent to positively charged atom involvement of neighbouring groups in hyperconjugation and resonace''.
Draw the possible resonance structures for `CH_(3) - underset(..)overset(..)(O) - overset(+)(C) H_(2)` and predict which of the structures is more stable. Give reason for your answer.

Explanation

Structure II is more stable because every atom has complete octet of electrons.