Organic Chemistry: Principles And Mechanisms (second Edition)
Organic Chemistry: Principles And Mechanisms (second Edition)
2nd Edition
ISBN: 9780393630749
Author: KARTY, Joel
Publisher: W. W. Norton & Company
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Chapter 13, Problem 13.12P
Interpretation Introduction

Interpretation:

How 3, 4-dimethylhex-2-ene can be synthesized via two different precursors, with the leaving group on C2 or on C3, is to be shown.

Concept introduction:

In a retrosynthetic analysis, the position and the substitution of the double bond in the product must be taken into account when determining the precursor. The substituents on the double bond and on the adjacent carbon atoms determine if the product is a Zaitsev product or a Hofmann product. This, in turn, will determine the position and nature of the leaving group and the nature of the base.

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Choose the Lewis structure for the compound below: H2CCHOCH2CH(CH3)2 HH H :d H H H C. Η H H HH H H H H. H H H HH H H H H H- H H H C-H H H HHHH
Each of the highlighted carbon atoms is connected to hydrogen atoms.
く Complete the reaction in the drawing area below by adding the major products to the right-hand side. If there won't be any products, because nothing will happen under these reaction conditions, check the box under the drawing area instead. Note: if the products contain one or more pairs of enantiomers, don't worry about drawing each enantiomer with dash and wedge bonds. Just draw one molecule to represent each pair of enantiomers, using line bonds at the chiral center. More... No reaction. Explanation Check O + G 1. Na O Me Click and drag to start drawing a structure. 2. H + 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility 000 Ar P
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