ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
10th Edition
ISBN: 9781259972348
Author: Carey
Publisher: MCG CUSTOM
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Chapter 21.1, Problem 1P
Interpretation Introduction

Interpretation:

The structural formulas for the enol isomers of each of the given compounds are to be stated.

Concept introduction:

Enol refers to an intermediate structure that consists of an alkene group connected with a hydroxyl group at one end of its double bond.

The formation of enol occurs when a molecule contains protons on its alpha carbon atom. The extraction of protons takes place from the alpha carbon atom of the molecule to form an enol.

If the higher priority group are present on the opposite side then it is termed as an E isomer, While if the higher priority group are present on the same side then it is termed as Z isomer.

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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 21 Solutions

ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<

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