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Dienes, Conjugated Pi Systems, and Pericyclic Reactions
1,3-Butadiene Orbital Energy and Nodes
Description
1,3-Butadiene shows how conjugated dienes gain stability through π molecular orbitals. Conjugated dienes have lower heats of hydrogenation than cumulated and isolated dienes, so they are more stable. The simplest conjugated diene is 1,3-butadiene, a four-carbon molecule with each carbon sp2-hybridized and each carbon carryin...
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Transcript
1,3-Butadiene is a conjugated system with four sp2 hybridized carbons, each with an unhybridized p orbital containing one electron.
A linear combination of the four unhybridized atomic p orbitals gives rise to four π molecular orbitals, two bonding and two antibonding.
The four π electrons occu...
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