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.

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter15: Radical Reactions

Section: Chapter Questions

Problem 14E

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