Laboratory Techniques in Organic Chemistry
Laboratory Techniques in Organic Chemistry
4th Edition
ISBN: 9781464134227
Author: Jerry R. Mohrig, David Alberg, Gretchen Hofmeister, Paul F. Schatz, Christina Noring Hammond
Publisher: W. H. Freeman
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Chapter 8, Problem 4Q
Interpretation Introduction

Interpretation:

When the same computational chemistry method is performed by two different students, the reason for the different values for conformations needs to be explained and the method of determining the lowest energy value in this case needs to be discussed.

Concept Introduction:

Chair-like conformation for cyclohexane molecule is a three-dimensional way of representing the molecule. This is a non-planar conformation with all the angles approximately equal to 109.5o. This is stable conformation because it has lower strain energy than the flat hexagonal shape. All the carbon centers are equivalent in the chair conformation. In the flat hexagonal shape, the wedge and dashed bonds represent the group attached directed away and towards the plane of paper respectively. In the chair conformation, these wedge and dashed bonds are axial and equatorial respectively.

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When an unknown amine reacts with an unknown acid chloride, an amide with a molecular mass of 163 g/mol (M* = 163 m/z) is formed. In the infrared spectrum, important absorptions appear at 1661, 750 and 690 cm. The 13C NMR and DEPT spectra are provided. Draw the structure of the product as the resonance contributor lacking any formal charges. 13C NMR DEPT 90 200 160 120 80 40 0 200 160 120 80 40 0 DEPT 135 T 200 160 120 80 40 0 Draw the unknown amide. Select Dow Templates More Frage

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Laboratory Techniques in Organic Chemistry

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