14) i) Provide the structure of the major organic product which results when (S)-2- iodopentane is treated with CN in DMF. Give the absolute configuration of the product. ii) Determine the major product that is formed when the below alkyl halide undergoes an El reaction: CH3 H₂C CH3

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
Chapter16: Aldehydes And Ketones
Section: Chapter Questions
Problem 16.45P: The following bicyclic ketone has two -carbons and three -hydrogens. When this molecule is treated...
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14) i) Provide the structure of the major organic product which results when (S)-2-
iodopentane is treated with CN in DMF. Give the absolute configuration of the
product.
ii) Determine the major product that is formed when the below alkyl halide undergoes
an El reaction:
CH3
CH3
H₂C
Transcribed Image Text:14) i) Provide the structure of the major organic product which results when (S)-2- iodopentane is treated with CN in DMF. Give the absolute configuration of the product. ii) Determine the major product that is formed when the below alkyl halide undergoes an El reaction: CH3 CH3 H₂C
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