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.9P
Interpretation Introduction

Interpretation:

The 1, 2- methyl shift involving (CH3)3CC+HCH3 is to be discussed.

Concept introduction:

In a 1, 2- alkyl shift, a CH or CC bond adjacent to a carbocation is broken, and the positive charge is rearranged. It moves to the C atom whose bond is broken.

The carbocation rearrangement involves single species, so the carbocation must have both HOMO and LUMO for orbital interaction. The HOMO is the σ orbital that connects to the migrating group, and the LUMO is the empty p orbital of the positively charged C atom. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) must have axial overlap or parallel overlap. The axial overlap between HOMO and LUMO has substantial net overlap, so this reaction is allowed. If the HOMO and LUMO do not have a substantial overlap, this overlap is forbidden.

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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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