The alkyl halide cis-1-bromo-4-methycyclohexane (A) undergoes a(c)substitution reaction when treated with H,0 to give a racemic mixturewhich is made up of product B and C.(i)What is a racemicmixture?(ii)Draw all the possible diastereoisomers of the compoundbelow.BrBr

We are given three part of an organic problem based on stereochemistry of organic molecules.

(c) The alkyl halide cis-1-bromo-4-methycyclohexane (A) undergoes a substitution reaction when treated with H,O to give a racemic mixture which is made up of product B and C. (i) What is a racemic mixture? (ii) Draw all the possible diastereoisomers of the compound below. Br Br

(c) The alkyl halide cis-1-bromo-4-methycyclohexane (A) undergoes a substitution reaction when treated with H,O to give a racemic mixture which is made up of product B and C. (i) What is a racemic mixture? (ii) Draw all the possible diastereoisomers of the compound below. Br Br

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

Chapter20: Dienes, Conjugated Systems, And Pericyclic Reactions

Section20.6: Sigmatropic Shifts

Problem 20.12P

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Question

The alkyl halide cis-1-bromo-4-methycyclohexane (A) undergoes a
(c)
substitution reaction when treated with H,0 to give a racemic mixture
which is made up of product B and C.
(i)
What is a racemic
mixture?
(ii)
Draw all the possible diastereoisomers of the compound
below.
Br
Br

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