What is most likely the initial retrosynthetic step from the target molecule in the given transformation (i.e., the last step of the synthesis)? o-or O Elimination of the dibromide to give an alkyne. Addition of Br₂ to a cis alkene. O Free radical bromination with Br₂ O Addition of Br₂ to a trans alkene.
What is most likely the initial retrosynthetic step from the target molecule in the given transformation (i.e., the last step of the synthesis)? o-or O Elimination of the dibromide to give an alkyne. Addition of Br₂ to a cis alkene. O Free radical bromination with Br₂ O Addition of Br₂ to a trans alkene.
Chapter20: Nucleophilic Substitution Reactions: Competing Nucleophiles
Section: Chapter Questions
Problem 2Q
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![What is most likely the initial retrosynthetic step from the target molecule in the given transformation (i.e., the last step of the
synthesis)?
Br
0-0
-or
Br
O Elimination of the dibromide to give an alkyne.
Addition of Br₂ to a cis alkene.
O Free radical bromination with Br₂
O Addition of Br₂ to a trans alkene.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F84b620de-0281-402f-aa6b-007ccbf2872b%2F42be1714-a272-4bb7-8173-6626efea25ab%2Fbtitqkg_processed.jpeg&w=3840&q=75)
Transcribed Image Text:What is most likely the initial retrosynthetic step from the target molecule in the given transformation (i.e., the last step of the
synthesis)?
Br
0-0
-or
Br
O Elimination of the dibromide to give an alkyne.
Addition of Br₂ to a cis alkene.
O Free radical bromination with Br₂
O Addition of Br₂ to a trans alkene.
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