Q17 · CSIR-NET Chemistry, December 2014

Paper: CSIR-NET December 2014 · Subject: Organic Chemistry · Chapter: Reagents, Reaction Mechanisms & Named Reactions · Topic: Named Reactions · Marks: 2 · Difficulty: Medium

The major product of the following reaction is: Question structure 1 of 5, ABC26OR0246 Question structure 2 of 5, ABC26OR0246 Question structure 3 of 5, ABC26OR0246 Question structure 4 of 5, ABC26OR0246 Question structure 5 of 5, ABC26OR0246
(a)Option (a) structure, ABC26OR0246
(b)Option (b) structure, ABC26OR0246
(c)Option (c) structure, ABC26OR0246
(d)Option (d) structure, ABC26OR0246
Answer
Answer: A ✓ checked by 4AB · confidence low

Skeleton certain; the relative stereochemistry of CN/COOEt between (a) and (b) is not decidable from the crop.

Explanation
The pyrrolidine enamine forms toward the less hindered CH₂ and is alkylated by the allylic bromide; after hydrolysis, base generates the other enolate (at the methyl-bearing carbon), which adds intramolecularly (Michael) to the cyanoacrylate, giving the azabicyclo[3.3.1]nonanone with the methyl at the bridgehead (a).

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1. Practise the PYQsPrevious-year questions, with answers

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