Connect Online Access 1-Semester for Organic Chemistry
Connect Online Access 1-Semester for Organic Chemistry
6th Edition
ISBN: 9781260475609
Author: SMITH, Janice
Publisher: Mcgraw-hill Higher Education (us)
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Chapter 22, Problem 54P
Interpretation Introduction

Interpretation: The stepwise mechanism for the given reaction is to be drawn.

Concept introduction: In crossed claisen condensation reaction, the base abstracts the acidic proton from α carbon atom of an ester to form enolate. This enolate reacts with carbonyl compound of other ester that leads to the formation of β-ketoester.

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For this question, if the product is racemic, input both enantiomers in the same Marvin editor. A) Input the number that corresponds to the reagent which when added to (E)-but-2-ene will result in a racemic product. Input 1 for Cl, in the cold and dark Input 2 for Oy followed by H₂O, Zn Input 3 for D₂ with metal catalyst Input 4 for H₂ with metal catalyst B) Draw the skeletal structure of the major organic product made from the reagent in part A Marvin JS Help Edit drawing C) Draw the skeletal structure of the major organic product formed when (2)-but-2-ene is treated with peroxyacetic acid. Marvin 35 Help
Michael Reactions 19.52 Draw the products from the following Michael addition reactions. 1. H&C CH (a) i 2. H₂O* (b) OEt (c) EtO H₂NEt (d) ΕΙΟ + 1. NaOEt 2. H₂O' H H 1. NaOEt 2. H₂O*

Chapter 22 Solutions

Connect Online Access 1-Semester for Organic Chemistry

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