ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS
ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS
6th Edition
ISBN: 9781264382545
Author: SMITH
Publisher: MCG CUSTOM
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Chapter 21.3, Problem 9P
Interpretation Introduction

Interpretation: The reason corresponding to the fact that organolithium reagents are not used to generate enolates is to be stated.

Concept Introduction: The substitution reaction involves the replacement of one functional group by other functional group. In nucleophilic substitution an electron rich species attack the species that is deficient in electrons. The electrophile and the leaving group together form a substrate. The nucleophile attacks over the substrate and there occurs the removal of leaving group from the substrate.

The nucleophilic reaction that consists of bimolecular as well as bond-making and bond-breaking steps is termed as SN2 reactions. This is a one-step reaction in which both nucleophile and substrate participate in the rate determining step.

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2) a) n-Butyllithium is used to deprotonate the following compounds. Draw the structures of the resulting organolithium compounds (assume they are monomeric). Me₂N SO₂ b) Explain the selectivity of deprotonation. c) Each organolithium is reacted with ethyltosylate. Draw the structures of the resulting products.
Why is it not advisable to use aqueous hydrochloric acid in a Grignard reaction of a ketone? A) The Grignard reagent will react with the acid and cannot react with the ketone. B) The ketone will be protonated and will become unreactive. C) The ketone will form an unreactive enol. D) The Grignard reagent won't dissolve in aqueous solutions
Modify the given structure and the product formed.

Chapter 21 Solutions

ORGANIC CHEM W/BIOLOGICAL TOP. ACCESS

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