When heated with a solution of sodium ethoxide in ethanol, compound A (C7H15Br) produces a mixture of two alkenes B and C, each of which has the molecular formula C7H14 . Catalytic hydrogenation of major isomer B or minor isomer C produces only 3-ethylpentane. Suggest the structures and mechanisms for compounds A, B, and C consistent with these observations
When heated with a solution of sodium ethoxide in ethanol, compound A (C7H15Br) produces a mixture of two alkenes B and C, each of which has the molecular formula C7H14 . Catalytic hydrogenation of major isomer B or minor isomer C produces only 3-ethylpentane. Suggest the structures and mechanisms for compounds A, B, and C consistent with these observations
General, Organic, and Biological Chemistry
7th Edition
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher:H. Stephen Stoker
Chapter14: Alcohols, Phenols And Ethers
Section: Chapter Questions
Problem 14.71EP: Three isomeric pentanols with unbranched carbon chains exist. Which of these isomers, upon...
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When heated with a solution of sodium ethoxide in ethanol, compound A (C7H15Br) produces a mixture of two
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