ORGANIC CHEM. VOL.1+2-W/WILEYPLUS
ORGANIC CHEM. VOL.1+2-W/WILEYPLUS
12th Edition
ISBN: 9781119304241
Author: Solomons
Publisher: WILEY C
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Chapter FRP, Problem 14P

Bromination of 2-methylbutane yields predominantly one product with the formula C 5 H 11 B r . What is this product? Show how you could use this compound to synthesize each of the following. (You need nor repeat seeps carried out in earlier parts.

(a) 2-Methyl-2-butene

(b) 2-Methyl-2-butanol

(c) 3-Methyl-2-butanol

(d) 3-Methyl-1-butyne

(e) 1-Bromo-3-methylbutane

(f) 2-Chloro-3-methylbutane

(g) 2-Chloro-2-methylbutane

(h) 1-Iodo-3-methylbutane

(i)

Chapter FRP, Problem 14P, Bromination of 2-methylbutane yields predominantly one product with the formula C5H11Br. What is

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How could you convert butanoic acid into the following compounds? Write each step showing the reagents needed. (a) 1-Butanol (b) 1-Bromobutane (c) 1-Butene
2-bromo-2-methylbutane undergoes hydrolysis reaction with water, H2O toform compound W. Compound X and compound Y are produced when 2-bromo-2-methylbutane undergoes elimination reaction with alcoholic ofsodium hydroxide, NaOH. (i) Draw the structural formula of compounds W, X and Y
(a) Why is the following reaction a poor method for synthesizing tert-butyl propyl ether? (b) What would be the major product of this reaction? (c) Propose a better synthesis of tert-butyl propyl ether. does not give CH3 CH,CH,CH,—O: Na + CH;–c–Br CH3 tert-butyl bromide odium propoxide CH3 CH₂-C-0-CH₂CH₂CH T CH3 tert-butyl propyl ether

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ORGANIC CHEM. VOL.1+2-W/WILEYPLUS

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