Essential Organic Chemistry, Global Edition
Essential Organic Chemistry, Global Edition
3rd Edition
ISBN: 9781292089034
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 16, Problem 41P
Interpretation Introduction

Interpretation:

The explanation corresponding to the given statement that 80% of Didose exists in the anhydrous form in an aqueous solution at 100°C, but only 0.1% of Didose exists in the anhydro form under the same condition has to be given.

Concept Introduction:

The chair conformers are stable forms of cyclic compounds.  In chair conformation, substituent’s prefers to place at equatorial positions.  This is due to unwanted interactions between those substituent’s that are placed at axial positions.  These interactions cause repulsion and that leads to the un-stability in molecule.  The general interactions that occur between axial substituents are 1,3 diaxial interactions.

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The most stable conformation of the pyranose ring of most D-aldohexoses places the largest group, CH2OH, in the equatorial position. An exception to this is the aldohexose D-idose. Draw the two possible chair conformations of either the a or B anomer of D-idose. Explain why the more stable conformation has the CH2OH group in the axial position.
The most stable conformation of the pyranose ring of most Daldohexosesplaces the largest group, CH2OH, in the equatorial position.An exception to this is the aldohexose D-idose. Draw the two possiblechair conformations of either the α or β anomer of D-idose. Explain whythe more stable conformation has the CH2OH group in the axial position .
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