) a) The radical chlorination of pentane is a poor way to prepare 1-chloropentane but radical chlorination of neopentane, (CH).C, is a good way to prepare neopentyl chloride, (CH),CCH;CI. Explain. b) Show the mechanism for the radical chlorination of neopentane. Illustrate homolytic bond

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter11: Ethers, Epoxides, And Sulfides
Section: Chapter Questions
Problem 11.18P
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)a) The radical chlorination of pentane is a poor way to prepare 1-chloropentane but radical
chlorination of neopentane, (CH).C, is a good way to prepare neopentyl chloride,
(CH) CCH;CI. Explain.
b) Show the mechanism for the radical chlorination of neopentane. Illustrate homolytic bond
cleavage and bond formation.
Transcribed Image Text:)a) The radical chlorination of pentane is a poor way to prepare 1-chloropentane but radical chlorination of neopentane, (CH).C, is a good way to prepare neopentyl chloride, (CH) CCH;CI. Explain. b) Show the mechanism for the radical chlorination of neopentane. Illustrate homolytic bond cleavage and bond formation.
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