ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT
ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT
12th Edition
ISBN: 9781119664635
Author: Solomons
Publisher: WILEY
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Chapter 10, Problem 32P

Synthesize each of die following compounds by routes that involve allylic or benzylic brominacion by NBS and any other synthetic steps necessary. Begin by writing a retrosynthetic analysis.

(a)

Chapter 10, Problem 32P, Synthesize each of die following compounds by routes that involve allylic or benzylic brominacion by , example  1

(b)

Chapter 10, Problem 32P, Synthesize each of die following compounds by routes that involve allylic or benzylic brominacion by , example  2

(c)

Chapter 10, Problem 32P, Synthesize each of die following compounds by routes that involve allylic or benzylic brominacion by , example  3

(d)

Chapter 10, Problem 32P, Synthesize each of die following compounds by routes that involve allylic or benzylic brominacion by , example  4

(e)

Chapter 10, Problem 32P, Synthesize each of die following compounds by routes that involve allylic or benzylic brominacion by , example  5

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Propose a synthesis for each of the following compounds. (a) OH (b) (c)
(a) What reagents would be used for the conversion of alkene A into the target? (b) What reaction is involved in the conversion of alcohol B into alkene A? Suggest a reagent that might affect this transformation. (c) Give a retrosynthetic analysis showing the disconnection of B, the synthons produced that lead to the synthetic equivalents given (draw their structures).
Guiding your reasoning by retrosynthetic analysis, show how you could prepare each of the following compounds from the given starting material and any necessary organic or inorganic reagents. All require more than one synthetic step. (a) Cyclopentyl iodide from cyclopentane (b) 1-Bromo-2-methylpropane from 2-bromo-2-methylpropane (c) meso-2,3-Dibromobutane from 2-butyne (d) 1-Heptene from 1-bromopentane (e) cis-2-Hexene from 1,2-dibromopentane (f) Butyl methyl ether (CH3CH2CH2CH2OCH3) from 1-butene
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