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Question

Write a short note on hyperconjugation and give all hyperconjugated structures of propene.

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Solution

Hyper-conjugation is the interaction of the electrons in a σ bond with an adjacent empty or partially filled non-bonding p-orbital, antibonding σ or π orbital or filled π orbital to give an extended molecular orbital that increases the stability of the system.
In case of propene, hyperconjugation arise due to partial overlap of sp3 sigma bond orbital and the empty p-orbital of an adjacent catom.
Here one of the C-atom CH bonds of CH3 group can lie in the plane of pi-bond orbital, hence partial overlapping.
See the given structure.

1123031_1130623_ans_41caa552bfc14e0bb3a2c74b077a686a.png

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