Organic Chemistry
Organic Chemistry
8th Edition
ISBN: 9781305580350
Author: William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher: Cengage Learning
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Chapter 25.3, Problem 25.4P
Interpretation Introduction

Interpretation:

To methyl α-D-mannopyranoside (methyl α-D-mannoside), Haworth projection and chair conformations has to be given and the anomeric carbon and the glycosidic bond has to be labelled.

Concept Introduction:

The aldehydes or ketones reacts with alcohol to form cyclic hemiacetal.  If hemiacetal reacts with another alcohol molecule it forms acetal.  Acetal is also known as glycoside.

The bond formed between the anomeric carbon and the alcohol molecule is said to be glycosidic bond.

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Draw the structure of:  a polysaccharide formed by joining D-mannose units in 1→4-β- glycosidic linkages;
Consider the following Haworth structure of a disaccharide and identify the type of glycosidic bond in it. a-1,6-glycosidic bond a-1,4-glycosidic bond a,ß-1,2-glycosidic bond O B-1,4-glycosidic bond H HO HOCH2 H CH₂OH H OH H H OH H OH OH H H CH₂OH
Draw the structures (using chair conformations of pyranoses) of the following disaccharides.  a-d-fructofuranosyl-b-d-mannopyranoside(
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