Ch CH¿CH2CH,CH; CH;CHCH,CH3 light ČI (1:1 Moar) i) Name the general type of reaction shown above. ii) The reaction proceeds via a free-radical mechanism. Show the mechanism for the formation of the chlorinated product above. iii) The chlorinated product has one chiral centre. Draw two enantiomers of this compound using perspective diagrams. iv) Identify the absolute configuration for each isomer. v) Give one way in which the two enantiomers could be distinguished.

Ch CH¿CH2CH,CH; CH;CHCH,CH3 light ČI (1:1 Moar) i) Name the general type of reaction shown above. ii) The reaction proceeds via a free-radical mechanism. Show the mechanism for the formation of the chlorinated product above. iii) The chlorinated product has one chiral centre. Draw two enantiomers of this compound using perspective diagrams. iv) Identify the absolute configuration for each isomer. v) Give one way in which the two enantiomers could be distinguished.

Introduction to General, Organic and Biochemistry

11th Edition

ISBN:9781285869759

Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres

Publisher:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres

Chapter19: Carboxylic Anhydrides, Esters, And Amides

Section: Chapter Questions

Problem 19.47P

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