Explain hyperconjugation in propylene molecule
Answers
Answered by
0
it has 4 hypervonjugated H atoms
Answered by
9
Explanation:
In the formalism that separates bonds into σ and π types, hyperconjugation is the interaction of σ-bonds (e.g. C-H, C-C, etc.) with a π network.
This interaction is customarily illustrated by contributing structures, e.g. for toluene (below), sometimes said to be an example of "heterovalent" or "sacrificial hyperconjugation", so named because the contributing structure contains one two-electron bond less than the normal Lewis formula for toluene.
Similar questions