2. Provide the product for the following reaction. Provide the sterochemistry an regiochemistry where is appropriate. Show the mechanism for C, and D. „CH3 HCI а) b) HCI HCI c)

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
Chapter8: Haloalkanes, Halogenation, And Radical Reactions
Section: Chapter Questions
Problem 8.32P
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parts a, b, c, d, and e

2. Provide the product for the following reaction. Provide the sterochemistry and
regiochemistry where is appropriate. Show the mechanism for C, and D.
„CH3
HCI
a)
b)
HCI
HCI
c)
d)
HBr
HCI
Transcribed Image Text:2. Provide the product for the following reaction. Provide the sterochemistry and regiochemistry where is appropriate. Show the mechanism for C, and D. „CH3 HCI a) b) HCI HCI c) d) HBr HCI
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Hello. Since the question contains multiple subparts the first three subparts are solved. In case the solution for other subparts are required, then repost the entire question and specify the subpart that has to be solved.

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a) 1-Methylcyclohexene on treatment with HCl gives 1-Chloro-1-methylcyclohexane. A molecule of HCl is added to the carbon-carbon double bond.

The addition of hydrogen halides to unsymmetrical alkene takes place according to Markovnikov’s rule. When an unsymmetrical reagent adds to an unsymmetrical alkene, the negative part of the reagent gets attached to that unsaturated carbon atom which carries a lesser number of hydrogen atoms.

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