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 16.6, Problem 10P

a)

Interpretation Introduction

Interpretation:

The structure of the given sugar β-D-galactopyranose is to be drawn by using Haworth projections.

Concept Introduction:

Concept introduction:

The Haworth projection: A Haworth projection is a three-dimensional representation of monosaccharides and the structural formula is inscription as a cyclic structures.

In Haworth projection, oxygen atom is placed in back right corner, CH2OH is arranged up at the C5 carbon atom. Anomeric hydroxyl group is placed down if it is α-anomer which is trans to the CH2OH of C5 carbon. The remaining hydroxyl group is placed up if the hydroxyl group left side in Fischer projection. Hydroxyl group is placed down if the hydroxyl group right side in Fischer projection

Furanose: A five-member closed chain form of a monosaccharide.

Pyranose: A six-member cyclic form of a monosaccharide.

b)

Interpretation Introduction

Interpretation:

The structure of the given sugar α-D-tagatopyranose is to be drawn by using Haworth projections.

Concept Introduction:

The Haworth projection: A Haworth projection is a three-dimensional representation of monosaccharides and the structural formula is inscription as a cyclic structures.

In Haworth projection, oxygen atom is placed in back right corner, CH2OH is arranged up at the C5 carbon atom. Anomeric hydroxyl group is placed down if it is α-anomer which is trans to the CH2OH of C5 carbon. The remaining hydroxyl group is placed up if the hydroxyl group left side in Fischer projection. Hydroxyl group is placed down if the hydroxyl group right side in Fischer projection

Furanose: A five-member closed chain form of a monosaccharide.

Pyranose: A six-member cyclic form of a monosaccharide.

c)

Interpretation Introduction

Interpretation: The structure of the given sugar α-D-Glucopyranose is to be drawn by using Haworth projections.

Concept Introduction:

The Haworth projection: A Haworth projection is a three-dimensional representation of monosaccharides and the structural formula is inscription as a cyclic structures.

In Haworth projection, oxygen atom is placed in back right corner, CH2OH is arranged up at the C5 carbon atom. Anomeric hydroxyl group is placed down if it is α-anomer which is trans to the CH2OH of C5 carbon. The remaining hydroxyl group is placed up if the hydroxyl group left side in Fischer projection. Hydroxyl group is placed down if the hydroxyl group right side in Fischer projection

Furanose: A five-member closed chain form of a monosaccharide.

Pyranose: A six-member cyclic form of a monosaccharide.

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Students have asked these similar questions
Draw the following sugars using Haworth projections: b. a-D-tagatopyranose a. c. B-D-galactopyranose c. a-L-glucopyranose
Answer the following questions about monosaccharide A.a. Draw the α anomer of A in a Haworth projection.b. Draw the β anomer of A in a three-dimensional representation using a chair conformation.c. What two aldoses yield A in a Wohl degradation?d. What product is formed when A undergoes a Wohl degradation?e. What product is formed when A reacts with Ag2O in NH4OH?
D-Arabinose can exist in both pyranose and furanose forms. a. Draw the α and β anomers of D-arabinofuranose. b. Draw the α and β anomers of D-arabinopyranose.
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