Get Ready for Organic Chemistry
Get Ready for Organic Chemistry
2nd Edition
ISBN: 9780321774125
Author: KARTY, Joel
Publisher: PEARSON
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Chapter D, Problem D.11YT
Interpretation Introduction

Interpretation:

The atomic orbital overlap and MO energy diagrams for CH3CH2Br (Figs. 3-13 through 3-25 to be reviewed) are to be constructed, and these diagrams are to be used to determine its HOMO and LUMO. Whether answers agree with the ones shown in Figure D-10a 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 C atoms and the Br atom are all sp3 hybridized, and each H atom contributes a 1s orbital. End-on overlap occurs in the C-H, C-C, and C-Br bonding and, therefore, results in seven σ bonds. When the 14 AOs overlap, 14 MOs are produced: seven σ bonding and seven σ* antibonding. This leaves three nonbonding orbitals.

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