Pearson eText Organic Chemistry -- Instant Access (Pearson+)
Pearson eText Organic Chemistry -- Instant Access (Pearson+)
9th Edition
ISBN: 9780135213728
Author: Leroy Wade, Jan Simek
Publisher: PEARSON+
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Chapter 14.7, Problem 14.13P

(a)

Interpretation Introduction

To determine: The formation of given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols.

Interpretation: The formation of given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols is to be identified.

Concept introduction: In a condensation reaction, two molecules join together to form a large molecule with the removal of small molecule such as water.

(b)

Interpretation Introduction

To determine: The formation of the given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols.

Interpretation: The formation of given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols is to be identified.

Concept introduction: The reaction of an alkoxide ion with 1° alkyl halide through SN2 mechanism to form ether is known as Williamson reaction.

(c)

Interpretation Introduction

To determine: The formation of given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols.

Interpretation: The formation of given ether in good yield by condensation of the corresponding alcohol and the alternative method for the ether that cannot be prepared by the condensation of the alcohols is to be identified.

Concept introduction: In alkoxymercuration-demercuration, ether is produced when alkene reacts with an alcohol in the presence of mercury acetate.

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Chapter 14 Solutions

Pearson eText Organic Chemistry -- Instant Access (Pearson+)

Ch. 14.7 - Explain why bimolecular condensation is a poor...Ch. 14.7 - Prob. 14.12PCh. 14.7 - Prob. 14.13PCh. 14.8 - Prob. 14.14PCh. 14.8 - Prob. 14.15PCh. 14.8 - Prob. 14.16PCh. 14.10A - Prob. 14.17PCh. 14.10A - Prob. 14.18PCh. 14.10B - Prob. 14.19PCh. 14.11B - Show how you would accomplish the following...Ch. 14.11B - Prob. 14.21PCh. 14.12 - Prob. 14.22PCh. 14.12 - Prob. 14.23PCh. 14.12 - Prob. 14.24PCh. 14.13 - Prob. 14.25PCh. 14.13 - Prob. 14.26PCh. 14.14 - Prob. 14.27PCh. 14.15 - Give the expected products of the following...Ch. 14 - Write structural formulas for the following...Ch. 14 - Give common names for the following compounds. a....Ch. 14 - Give IUPAC names for the following compounds. a....Ch. 14 - Glycerol (propane-1,2,3-triol) is a viscous syrup...Ch. 14 - Prob. 14.33SPCh. 14 - Show how you would make the following ethers,...Ch. 14 - (A true story.) An inexperienced graduate student...Ch. 14 - Prob. 14.36SPCh. 14 - a. Show how you would synthesize the pure (R)...Ch. 14 - a. Predict the values of m/z and the structures of...Ch. 14 - The following reaction resembles the...Ch. 14 - Prob. 14.40SPCh. 14 - Prob. 14.41SPCh. 14 - Prob. 14.42SPCh. 14 - Give the structures of the intermediates...Ch. 14 - Prob. 14.44SPCh. 14 - Show how you would synthesize the following ethers...Ch. 14 - Prob. 14.46SPCh. 14 - Prob. 14.47SPCh. 14 - Prob. 14.48SPCh. 14 - An acid-catalyzed reaction was carried out using...Ch. 14 - Propylene oxide is a chiral molecule. Hydrolysis...Ch. 14 - Prob. 14.51SPCh. 14 - Prob. 14.52SPCh. 14 - Prob. 14.53SPCh. 14 - Prob. 14.54SPCh. 14 - In 2012, a group led by Professor Masayuki Satake...
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