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Show how free-radical halogenation might be used to

Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr ISBN: 9780321768414 33

Solution for problem 10P Chapter 6

Organic Chemistry | 8th Edition

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Organic Chemistry | 8th Edition | ISBN: 9780321768414 | Authors: L.G. Wade Jr

Organic Chemistry | 8th Edition

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Problem 10P

Show how free-radical halogenation might be used to synthesize the following compounds. Ineach case, explain why we expect to get a single major product.

(a) 1-chloro-2,2-dimethylpropane (neopentyl chloride)

(b) 2-bromo-2-methylbutane

(c)

(d) 

Step-by-Step Solution:
Step 1 of 3

Step-1

(a) Free-radical halogenation 1-chloro-2,2-dimethylpropane (neopentyl chloride)

Here all the H atoms are similar i.e only one type of present in this compound so that only one monochlorine isomer has formed.

Step-2

(b) 2-bromo-2-methylbutane

Here the single major product has formed  because bromination involves removal of H atom and formed...

Step 2 of 3

Chapter 6, Problem 10P is Solved
Step 3 of 3

Textbook: Organic Chemistry
Edition: 8
Author: L.G. Wade Jr
ISBN: 9780321768414

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