Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Chapter FRP, Problem 31P
Interpretation Introduction

Interpretation:

The product of each of the given reactions is to be predicted.

Concept introduction:

Lithium aluminum hydride reduces ketones, esters, and cyclic esters (lactones) to alcohols.

In the Williamson ether synthesis, alkoxides attack the alkyl halides to form ethers.

Chromic acid oxidizes primary alcohols to form carboxylic acids.

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(c) Answer each of the questions below that relate to acetophenone: Xo (i) (ii) (iii) Draw the structure of the enol form of acetophenone. Give a stepwise mechanism for the conversion of acetophenone into its enol form. Show how each of the three compounds A, B and C below can be prepared from acetophenone. Explain clearly what reactants/reagents would be required in each case. odocor A B Br C
Predict the major organic product of each of the following reactions or provide the reagent needed to complete each transformation.
Predict the major product or the necessary reagent or reactant to complete each of the following reactions. In the box before each reaction, indicate the mechanism followed by the reaction. (Free radical (FR), SN2, SN1). (b) (a) Cl₂ CH₂CH₂OH (a) 1 hv 2 (b) H Br H₂O Na+ SCH3 (c) (d) CI "CH3

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Organic Chemistry

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