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.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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I have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."
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Linear Combination of Atomic Orbitals LCAO; Author: Edmerls;https://www.youtube.com/watch?v=nq1zwrAIr4c;License: Standard YouTube License, CC-BY
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