ORGANIC CHEMISTRY (LL)-PACKAGE
ORGANIC CHEMISTRY (LL)-PACKAGE
8th Edition
ISBN: 9781319316389
Author: VOLLHARDT
Publisher: MAC HIGHER
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Chapter 6.6, Problem 6.17E
Interpretation Introduction

Interpretation: The starting material of each of the two examples in the textbook should be replaced with one of its diastereomers and the product of SN2 displacement with the nucleophile shown should be written.

Concept Introduction:

Diastereomers are stereoisomers which are not mirror images of one another. Stereoisomers with two or more stereocenters can be diastereomers.

SN2 reactions are a type of nucleophilic substitution reactions. In SN2reactions, the addition of the nucleophile and the departure of the leaving group occur simultaneously. So, the nucleophile attacks the molecule from the opposite side of the leaving group. As a result, the geometry of the molecule changes and the stereochemical configuration of the molecule is inverted.

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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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