ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
10th Edition
ISBN: 9781260008562
Author: Carey
Publisher: MCG
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Chapter 21, Problem 36P
Interpretation Introduction

Interpretation:

The structure of the product for the given reaction is to be drawn.

Concept introduction:

Aldehydes and ketones contain carbonyl (C=O) functional group in their parent chain. The halogenation of aldehyde or ketone takes place by the replacement of alpha proton to the carbonyl group by halogen.

The compounds that contain two ketone groups are commonly known as β-Diketones. The reaction in which the addition of an alpha carbon of an enolizable aldehyde or ketone to the carbonyl group of the second aldehyde or group takes place to form β-hydroxy carbonyl compounds, such reaction is called as the aldol reaction.

The Organolithium cuprates (R2CuLi) are used for the 1,4- addition or conjugate addition to the α,β- unsaturated carbonyl compounds. The conjugated ketone is attacked by the nucleophilic carbon atom of the cuprate at the electrophilic carbon of alkene through nucleophilic addition reaction.

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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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