Q16 · CSIR-NET Chemistry, December 2015

Paper: CSIR-NET December 2015 · Subject: Organic Chemistry · Chapter: Reagents, Reaction Mechanisms & Named Reactions · Topic: Reagents, Reaction Mechanisms & Named Reactions – General · Marks: 2 · Difficulty: Medium

The major product formed in the following reaction sequence is: Question structure 1 of 2, ABC26OR0274 Question structure 2 of 2, ABC26OR0274
(a)Option (a) structure, ABC26OR0274
(b)Option (b) structure, ABC26OR0274
(c)Option (c) structure, ABC26OR0274
(d)Option (d) structure, ABC26OR0274
Answer
Answer: D ✓ checked by 4AB · confidence medium
Explanation
PhSeCl on 1,5-cyclooctadiene triggers transannular cyclisation: the episelenonium ion is captured by the second alkene and acetate traps the cation, giving the cis-bicyclo[3.3.0]octane acetoxy-selenide; H₂O₂ oxidation and selenoxide syn-elimination give the acetoxy-bicyclo[3.3.0]octene (d).

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