9.9. Reaction of 3,5,5-trimethylcyclohex-2-en-1-one with NaNH₂ (3 equiv) in TH generates an enolate. When bromobenzene is added to this solution and stirr for 4 h, a product 9-A is isolated in 30% yield. Formulate a mechanism f this reaction. CH3 CH3 HO 9-A CH3

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter30: Orbitals And Organic Chemistry: Pericyclic Reactions
Section30.SE: Something Extra
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Hi i need a detailed mechanism
9.9. Reaction of 3,5,5-trimethylcyclohex-2-en-1-one with NaNH₂ (3 equiv) in THF
generates an enolate. When bromobenzene is added to this solution and stirred
for 4 h, a product 9-A is isolated in 30% yield. Formulate a mechanism for
this reaction.
CH3
S
9-A
HO
CH3
CH3
Transcribed Image Text:9.9. Reaction of 3,5,5-trimethylcyclohex-2-en-1-one with NaNH₂ (3 equiv) in THF generates an enolate. When bromobenzene is added to this solution and stirred for 4 h, a product 9-A is isolated in 30% yield. Formulate a mechanism for this reaction. CH3 S 9-A HO CH3 CH3
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