Q20 · CSIR-NET Chemistry, December 2012

Paper: CSIR-NET December 2012 · Subject: Organic Chemistry · Chapter: Reagents, Reaction Mechanisms & Named Reactions · Topic: Reagents, Reaction Mechanisms & Named Reactions – General · Marks: 2 · Difficulty: Medium

Under review — part of this question (a structure or an option) is not clear in the source scan. 4AB is checking it against the original book; the answer shown may change.
In the following reaction A and B are Question structure 1 of 3, ABC26OR0210 Question structure 2 of 3, ABC26OR0210 Question structure 3 of 3, ABC26OR0210
(a)Option (a) structure 1 of 4, ABC26OR0210 Option (a) structure 2 of 4, ABC26OR0210 Option (a) structure 3 of 4, ABC26OR0210 Option (a) structure 4 of 4, ABC26OR0210
(b)Option (b) structure, ABC26OR0210
(c)Option (c) structure, ABC26OR0210
(d)Option (d) structure, ABC26OR0210
Answer
Under review — not yet confirmed.
Answer: A
Explanation
i-PrMgCl deprotonates oxazole at its most acidic C-2 to give 2-oxazolylmagnesium chloride (A); the Weinreb amide then gives the 2-butanoyl oxazole (B) — (a).

Study loop for Reagents, Reaction Mechanisms & Named Reactions

1. Practise the PYQsPrevious-year questions, with answers

· Browse this chapter in the app