The S isomer of 2-chlorobutame (below) can react with chlorine to make 5 isomers of dichlorobutane. Draw a Fisher projection each isomer, label all of the chiral centers as R or S, and designate the enantiomer and diastereomer relationships. (This is a reaction you have never seen before, it is capable of removing any hydrogen in the molecule and replacing it with a chlorine. It is a 2,step reaction with a free radical intermediate) CH, -CI + Н-с-н Ch C4H3 Ch + HCI CH,

The S isomer of 2-chlorobutame (below) can react with chlorine to make 5 isomers of dichlorobutane. Draw a Fisher projection each isomer, label all of the chiral centers as R or S, and designate the enantiomer and diastereomer relationships. (This is a reaction you have never seen before, it is capable of removing any hydrogen in the molecule and replacing it with a chlorine. It is a 2,step reaction with a free radical intermediate) CH, -CI + Н-с-н Ch C4H3 Ch + HCI CH,

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

Chapter5: Alkenes: Bonding, Nomenclature, And Properties

Section: Chapter Questions

Problem 5.36P

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