ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
10th Edition
ISBN: 9781260008562
Author: Carey
Publisher: MCG
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Chapter 21.8, Problem 28P
Interpretation Introduction

Interpretation:

The two ways for the preparation of 4-methyl-2-octanone through conjugate addition of an organocuprate to an α,β- unsaturated ketone is to be determined.

Concept Introduction:

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Retrosynthesis is used to identify the reactants. It involves the breaking of the target molecule into starting materials.

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The Organolithium cuprates (R2CuLi) are used in the reaction that involves the 1,4- addition or conjugate addition to the α,β- unsaturated carbonyl compounds.

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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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