A ketone was converted to an alkene using a Wittig reaction. As part of this synthesis, the ylide was prepared from an alkyl bromide. What is the alkyl bromide that was used to prepare the ylide for this synthesis? O 2-bromopentane 1-bromopropane bromoethane 3-bromopentane
A ketone was converted to an alkene using a Wittig reaction. As part of this synthesis, the ylide was prepared from an alkyl bromide. What is the alkyl bromide that was used to prepare the ylide for this synthesis? O 2-bromopentane 1-bromopropane bromoethane 3-bromopentane
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
Chapter8: Haloalkanes, Halogenation, And Radical Reactions
Section: Chapter Questions
Problem 8.33P
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![A ketone was converted to an alkene
using a Wittig reaction. As part of this
synthesis, the ylide was prepared from an
alkyl bromide. What is the alkyl bromide
that was used to prepare the ylide for this
synthesis?
2-bromopentane
O 1-bromopropane
bromoethane
3-bromopentane](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F515c636f-ad9a-47e1-bca0-48b4b19764b0%2F0e3cd017-c49c-43e7-926c-c03d8a007581%2Fd7k8hpd_processed.png&w=3840&q=75)
Transcribed Image Text:A ketone was converted to an alkene
using a Wittig reaction. As part of this
synthesis, the ylide was prepared from an
alkyl bromide. What is the alkyl bromide
that was used to prepare the ylide for this
synthesis?
2-bromopentane
O 1-bromopropane
bromoethane
3-bromopentane
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