The rate of elimination of cis-1-bromo-4(1,1-dimethyl)cyclohexane is proportional to the concentration of both substrate and base, but that of the trans isomer is proportional only to the concentration of the substrate. a) draw the structures of cis and trans 1-bromo-4(1,1,-dimethyl)cyclohexane b) explain the difference in kinetics between the elimination reaction of cis and trans isomers.

The rate of elimination of cis-1-bromo-4(1,1-dimethyl)cyclohexane is proportional to the concentration of both substrate and base, but that of the trans isomer is proportional only to the concentration of the substrate. a) draw the structures of cis and trans 1-bromo-4(1,1,-dimethyl)cyclohexane b) explain the difference in kinetics between the elimination reaction of cis and trans isomers.

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

Chapter4: Acids And Bases

Section: Chapter Questions

Problem 4.22P: In each of the following three reaction coordinate diagrams, state: (a) Whether the reaction is...

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