Q17 · CSIR-NET Chemistry, June 2015

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

The products A and B in the following reaction sequence are Question structure 1 of 6, ABC26OR0257 Question structure 2 of 6, ABC26OR0257 Question structure 3 of 6, ABC26OR0257 Question structure 4 of 6, ABC26OR0257 Question structure 5 of 6, ABC26OR0257 Question structure 6 of 6, ABC26OR0257
(a)Option (a) structure 1 of 3, ABC26OR0257 Option (a) structure 2 of 3, ABC26OR0257 B = Option (a) structure 3 of 3, ABC26OR0257
(b)Option (b) structure 1 of 4, ABC26OR0257 Option (b) structure 2 of 4, ABC26OR0257 Option (b) structure 3 of 4, ABC26OR0257 Option (b) structure 4 of 4, ABC26OR0257
(c)Option (c) structure 1 of 3, ABC26OR0257 Option (c) structure 2 of 3, ABC26OR0257 B = Option (c) structure 3 of 3, ABC26OR0257
(d)Option (d) structure 1 of 4, ABC26OR0257 Option (d) structure 2 of 4, ABC26OR0257 Option (d) structure 3 of 4, ABC26OR0257 Option (d) structure 4 of 4, ABC26OR0257
Answer
Answer: B ✓ checked by 4AB · confidence medium
Explanation
KH/18-crown-6 triggers an anionic oxy-Cope through a chair TS, giving the δ,ε-unsaturated aldehyde A with the two methyls syn. The non-stabilised ylide gives the Z-alkene in B (b).

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