Q12 · CSIR-NET Chemistry, December 2014

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

The major product formed in the following transformation is: Question structure 1 of 4, ABC26OR0240 Question structure 2 of 4, ABC26OR0240 Question structure 3 of 4, ABC26OR0240 Question structure 4 of 4, ABC26OR0240
(a)Option (a) structure, ABC26OR0240
(b)Option (b) structure, ABC26OR0240
(c)Option (c) structure, ABC26OR0240
(d)Option (d) structure, ABC26OR0240
Answer
Answer: A ✓ checked by 4AB · confidence medium
Explanation
Bu₂BOTf/i-Pr₂NEt forms the Z-boron enolate, which undergoes an Evans syn-aldol through a Zimmerman–Traxler chair. The (4R,5S)-norephedrine-derived auxiliary sets the absolute configuration of the syn product (a).

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