Organic Chemistry Study Guide and Solutions
Organic Chemistry Study Guide and Solutions
6th Edition
ISBN: 9781936221868
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
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Chapter 10, Problem 10.4P
Interpretation Introduction

(a)

Interpretation:

The alkene formed by the acid-catalyzed dehydration reaction of 3- methyl -3- heptanol is to be stated.

Concept introduction:

The dehydration of alcohol leads to the formation of the alkene. This dehydration can be done by the acid-catalyzed mechanism. In this mechanism, the first step is the abstraction of a proton by the hydroxide group. The second step is the removal of water to give an intermediate “carbocation”. The third step is the generation of an alkene by the removal of β- hydrogen from the intermediate.

Interpretation Introduction

(b)

Interpretation:

The alkene(s) formed by the acid-catalyzed dehydration reaction of 1, 2- diphenyl -1- ethanol is to be stated.

Concept introduction:

The dehydration of alcohol leads to the formation of the alkene. This dehydration can be done acid-catalyzed mechanism. In this mechanism first step is the abstraction of a proton by the hydroxide group. The second step is the removal of water to give an intermediate “carbocation”. The third step is the generation of an alkene by the removal of β- hydrogen from the intermediate.

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个 ^ Blackboard x Organic Chemistry II Lecture (m x Aktiv Learning App x → C app.aktiv.com ← Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Problem 28 of 35 :OH H HH KO Select to Edit Arrows CH CH₂OK, CH CH2OH 5+ H :0: Done

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Organic Chemistry Study Guide and Solutions

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