Organic Chemistry
Organic Chemistry
6th Edition
ISBN: 9781936221349
Author: Marc Loudon, Jim Parise
Publisher: W. H. Freeman
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Chapter 19, Problem 19.62AP
Interpretation Introduction

(a)

Interpretation:

The product of the reaction of epoxide with LiAlD4 is to be stated.

Concept introduction:

Lithium aluminum hydride is a strong reducing agent. It is an inorganic compound which is used as the reducing agent in organic synthesis. Lithium aluminum hydride reduces epoxides to alcohols.

Interpretation Introduction

(b)

Interpretation:

The product of the reaction of epoxide with LiAlH4 is to be stated.

Concept introduction:

Lithium aluminum hydride is a strong reducing agent. It is an inorganic compound which is used as the reducing agent in organic synthesis. Lithium aluminum hydride reduces epoxides to alcohols.

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Students have asked these similar questions
(a) The Friedel-Crafts reaction of benzene with 2-chloro-3-methylbutane in the presence of AlCl3 occurs with a carbocation rearrangement. Give mechanistic explanation and the product formed. (b) Predict the product(s) will be formed from the following reactions: (i) Bromination of p-methylbenzoic acid (ii) Sulphonation of m-bromoanisole (iii) Friedel-craft acylation of o-bromonitrobenzene
Provide the reagents and solvents (where appropriate) needed to bring about the following transformations. (a) CI (b)
Predict the products of reactions of ethers and epoxides, including the following:(a) Cleavage and autoxidation of ethers(b) Acid- and base-promoted opening of epoxides(c) Reactions of epoxides with organometallic reagents(d) Cleavage of silyl ethers

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Organic Chemistry

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