2) Synthesizing the target molecule (below), it is suggested to start from the epoxide and benzene shown. In one step of the synthesis (Reaction 1), the ring closure occurs under acidic conditions. What reaction mechanism motif is Reaction 1 undergoing? What reagents would be used to finish the synthesis (Reaction 2)? H* Reaction 1 Reaction 2

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 16.63P
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2) Synthesizing the target molecule (below), it is suggested to start from the epoxide and benzene
shown. In one step of the synthesis (Reaction 1), the ring closure occurs under acidic conditions.
What reaction mechanism motif is Reaction 1 undergoing? What reagents would be used to finish
the synthesis (Reaction 2)?
H*
Reaction 1
Reaction 2
Transcribed Image Text:2) Synthesizing the target molecule (below), it is suggested to start from the epoxide and benzene shown. In one step of the synthesis (Reaction 1), the ring closure occurs under acidic conditions. What reaction mechanism motif is Reaction 1 undergoing? What reagents would be used to finish the synthesis (Reaction 2)? H* Reaction 1 Reaction 2
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