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

9th Edition

ISBN: 9780135213728

Author: Leroy Wade, Jan Simek

Publisher: PEARSON+

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Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic…

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Textbook Question

Chapter 21, Problem 21.54SP

Show how you would accomplish the following syntheses. Some of these conversions may require more than one step.

a. isopentylalcohol → isopentyl acetate (banana oil)
b. 3 – ethylpentanoicacid → 3 – ethylpentanenitrile
c. isobutylamine → N - isobutylformamide
d. ethyl acetate → 3 - methylpentan - 3 - ol
e. cyclohexylamine → N – cyclohexylacetamide
f. bromocyclohexane → dicyclohexylmethanol

Chapter 21, Problem 21.54SP, Show how you would accomplish the following syntheses. Some of these conversions may require more , example 1

Chapter 21, Problem 21.54SP, Show how you would accomplish the following syntheses. Some of these conversions may require more , example 2

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Chapter 21, Problem 21.53SP

Chapter 21, Problem 21.55SP

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Chapter 21 Solutions

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

Ch. 21.2F - Name the following carboxylic acid derivatives,...Ch. 21.4A - Prob. 21.2P Ch. 21.4A - Prob. 21.3P Ch. 21.4A - Prob. 21.4P Ch. 21.5C - Prob. 21.7P Ch. 21.6 - When ethyl 4-hydroxybutyrate is heated in the...Ch. 21.6 - Propose a mechanism for the following ring-opening...Ch. 21.6 - Prob. 21.15P Ch. 21.7B - Prob. 21.16P Ch. 21.7C - Prob. 21.19P

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Solution Summary: The author explains that the conversion of alcohol into ester is completed by the reaction of an alcohol with acetic anhydride.

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Chapter 21 Solutions