4-42 For each alkane, 1. Draw all the possible monochlorinated derivatives. 2. Determine whether free-radical chlorination would be a good way to make any of these monochlorinated derivatives. (Will the reaction give mostly one major product?) 3. Which monobrominated derivatives could you form in good yield by free-radical bromination? (a) cyclopentane (c) 2-methylpentane (b) methylcyclopentane (d) 2,2,3,3-tetramethylbutane

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter10: Organohalides
Section10.SE: Something Extra
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4-42
For each alkane,
1. Draw all the possible monochlorinated derivatives.
2. Determine whether free-radical chlorination would be a good way to make any of these monochlorinated derivatives.
(Will the reaction give mostly one major product?)
3. Which monobrominated derivatives could you form in good yield by free-radical bromination?
(a) cyclopentane
(c) 2-methylpentane
(b) methylcyclopentane
(d) 2,2,3,3-tetramethylbutane
Transcribed Image Text:4-42 For each alkane, 1. Draw all the possible monochlorinated derivatives. 2. Determine whether free-radical chlorination would be a good way to make any of these monochlorinated derivatives. (Will the reaction give mostly one major product?) 3. Which monobrominated derivatives could you form in good yield by free-radical bromination? (a) cyclopentane (c) 2-methylpentane (b) methylcyclopentane (d) 2,2,3,3-tetramethylbutane
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