EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
2nd Edition
ISBN: 9780393630817
Author: KARTY
Publisher: W.W.NORTON+CO. (CC)
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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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Redraw the molecule below as a skeletal ("line") structure. Be sure to use wedge and dash bonds if necessary to accurately represent the direction of the bonds to ring substituents. Cl. Br Click and drag to start drawing a structure. : ☐ ☑ P
K m Choose the best reagents to complete the following reaction. L ZI 0 Problem 4 of 11 A 1. NaOH 2. CH3CH2CH2NH2 1. HCI B OH 2. CH3CH2CH2NH2 DII F1 F2 F3 F4 F5 A F6 C CH3CH2CH2NH2 1. SOCl2 D 2. CH3CH2CH2NH2 1. CH3CH2CH2NH2 E 2. SOCl2 Done PrtScn Home End FA FQ 510 * PgUp M Submit PgDn F11
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