Organic Chemistry
Organic Chemistry
8th Edition
ISBN: 9781305580350
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
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Chapter 29.6, Problem DQ
Interpretation Introduction

Interpretation:

The reaction involved in the synthesis of cyanoacrylates has to be given from the given set of options.

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What explains why many aldehydes and ketones can undergo self- condensation reactions in basic conditions? A. The alpha carbon can lose a proton and act like a nucleophile and the carbonyl carbon a an electrophile B. The alpha carbon can gain a proton and act like an electrophile and the carbonyl carbon is a nucleophile C. The oxygen of the carbonyl group can attack the carbon of the carbonyl group D. Only esters can undergo self-condensation reactions
Draw the major product of this reaction. Ignore inorganic byproducts. 1. Hg(OAc)2, H2O 2. NaBH4, NaOH
Give the product for each step in the reaction
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