ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
10th Edition
ISBN: 9781260008562
Author: Carey
Publisher: MCG
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Chapter 21, Problem 31P
Interpretation Introduction

Interpretation:

The structural formula for the enol form of diethyl malonate has to be drawn, the structural formulas for three enols of ethyl acetoacetate have to be drawn, among them, the most and least stable isomer has to be identified and the products of the reaction of bromine with both diethyl malonate and ethyl acetoacetate are to be stated.

Concept introduction:

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

The percentage of enol in keto-enol tautomerism depends upon the stability of enol formed.

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Transmitance 3. Which one of the following compounds corresponds to this IR spectrum? Point out the absorption band(s) that helped you decide. OH H3C OH H₂C CH3 H3C CH3 H3C INFRARED SPECTRUM 0.8- 0.6 0.4- 0.2 3000 2000 1000 Wavenumber (cm-1) 4. Consider this compound: H3C On the structure above, label the different types of H's as A, B, C, etc. In table form, list the labeled signals, and for each one state the number of hydrogens, their shifts, and the splitting you would observe for these hydrogens in the ¹H NMR spectrum. Label # of hydrogens splitting Shift (2)
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Chapter 21 Solutions

ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE

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