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 22, Problem 22.17P
Interpretation Introduction

Interpretation:

It is to be shown how to synthesize the given compound using benzene as the only aromatic starting compound.

Concept introduction:

When the aromatic species are treated with an acid chloride in the presence of a Lewis acid (e.g. AlCl3), an acylation takes place at the aromatic ring; it is called a Friedel-Crafts acylation reaction. The limitations of a Friedel-Crafts alkylation reaction are carbocation rearrangement; thus it is not a much suitable method for alkylation. A Friedel-Crafts acylation reaction is used to circumvent this problem, which gives an aromatic ketone as the product instead of any carbocation rearrangement reaction. This carbonyl group is then reduced by the Clemmensen reduction to form an alkylbenzene.

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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

Chapter 22 Solutions

Organic Chemistry: Principles And Mechanisms (second Edition)

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