Organic Chemistry: Principles and Mechanisms (Second Edition)
Organic Chemistry: Principles and Mechanisms (Second Edition)
2nd Edition
ISBN: 9780393663556
Author: Joel Karty
Publisher: W. W. Norton & Company
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Chapter D, Problem D.13YT
Interpretation Introduction

Interpretation:

The atomic orbital overlap and MO energy diagrams for CH3CH=CHCH3 (Figs. 3-13 through 3-25 to be reviewed) are to be constructed, and these diagrams are to be used to determine its HOMO. Whether the answer agrees with the one shown in Figure D-11 is to be explained.

Concept introduction:

Molecular orbitals are constructed from the AOs of different atoms. When two atoms are brought close enough together (i.e., about a bond length apart), the AOs of one atom significantly overlap the AOs of the other atom, enabling them to undergo constructive and destructive interference, or mix, to produce new orbitals. The two central C atoms are both sp2 hybridized and each has an unhybridized p orbital. The CH3 carbons are sp3 hybridized, and the H atoms each contribute a 1s orbital. End-on overlap occurs in the C-H and C-C bonding and, therefore, results in 11 σ bonds. Side-on overlap occurs between the two p orbitals of the two sp2- hybridized C atoms. This results in π bonding and π* antibonding. When the 24 AOs overlap, 24 MOs are produced: 11σ bonding, 11 σ* antibonding, one π bonding, and one π* antibonding. When the 24 total valence electrons fill the MOs, the π MO is the HOMO, and the π* MO is the LUMO.

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