Q21 · 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: Hard

The major product formed in following reaction sequence is Question structure 1 of 5, ABC26OR0261 Question structure 2 of 5, ABC26OR0261 Question structure 3 of 5, ABC26OR0261 Question structure 4 of 5, ABC26OR0261 Question structure 5 of 5, ABC26OR0261
(a)Option (a) structure, ABC26OR0261
(b)Option (b) structure, ABC26OR0261
(c)Option (c) structure, ABC26OR0261
(d)Option (d) structure, ABC26OR0261
Answer
Answer: D ✓ checked by 4AB · confidence high
Explanation
Photolysis of the α-diazoketone gives a Wolff rearrangement to a ketene, which undergoes [2+2] with the silyl ynol ether; the cyclobutenone opens (4π) to a vinylketene and closes (6π) onto the aryl ring — the Danheiser benzannulation — giving the phenol (d) with the three CH₂ groups of the starting seven-membered ring intact.

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