Haworth projection of α -pyranose form of the D-aldohexose should be drawn. 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, C H 2 O H is arranged up at the C5 carbon atom. Anomeric hydroxyl group is placed down if it is α-anomer which is trans to the C H 2 O H 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. Epimer: Epimer is one of a pair of stereoisomers. The two isomers differ in configuration at only one stereogenic center. To find : Haworth projection for α -pyranose form of the D-aldohexose

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Answer 1

Question

Chapter 24, Problem 54PP

Interpretation Introduction

Interpretation:

Haworth projection of α -pyranose form of the D-aldohexose should be drawn.

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.

Epimer: Epimer is one of a pair of stereoisomers. The two isomers differ in configuration at only one stereogenic center.

To find: Haworth projection for α -pyranose form of the D-aldohexose

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Answer 2

Question

Chapter 24, Problem 54PP

Interpretation Introduction

Interpretation:

Haworth projection of α -pyranose form of the D-aldohexose should be drawn.

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.

Epimer: Epimer is one of a pair of stereoisomers. The two isomers differ in configuration at only one stereogenic center.

To find: Haworth projection for α -pyranose form of the D-aldohexose

Expert Solution & Answer

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Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 24, Problem 54PP

Interpretation Introduction

Interpretation:

Haworth projection of α -pyranose form of the D-aldohexose should be drawn.

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.

Epimer: Epimer is one of a pair of stereoisomers. The two isomers differ in configuration at only one stereogenic center.

To find: Haworth projection for α -pyranose form of the D-aldohexose

Expert Solution & Answer

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Answer 4

Question

Chapter 24, Problem 54PP

Interpretation Introduction

Interpretation:

Haworth projection of α -pyranose form of the D-aldohexose should be drawn.

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.

Epimer: Epimer is one of a pair of stereoisomers. The two isomers differ in configuration at only one stereogenic center.

To find: Haworth projection for α -pyranose form of the D-aldohexose

Expert Solution & Answer

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Check out a sample textbook solution

See solution

Answer 5

Chapter 24, Problem 54PP

Interpretation Introduction

Interpretation:

Haworth projection of α -pyranose form of the D-aldohexose should be drawn.

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.

Epimer: Epimer is one of a pair of stereoisomers. The two isomers differ in configuration at only one stereogenic center.

To find: Haworth projection for α -pyranose form of the D-aldohexose

Answer 6

Chapter 24, Problem 54PP

Interpretation Introduction

Interpretation:

Haworth projection of α -pyranose form of the D-aldohexose should be drawn.

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.

Epimer: Epimer is one of a pair of stereoisomers. The two isomers differ in configuration at only one stereogenic center.

To find: Haworth projection for α -pyranose form of the D-aldohexose

Answer 7

Chapter 24, Problem 54PP

Interpretation Introduction

Interpretation:

Haworth projection of α -pyranose form of the D-aldohexose should be drawn.

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.

Epimer: Epimer is one of a pair of stereoisomers. The two isomers differ in configuration at only one stereogenic center.

To find: Haworth projection for α -pyranose form of the D-aldohexose

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 24.2 - Prob. 1CC Ch. 24.2 - Prob. 2CC Ch. 24.2 - Prob. 3CC Ch. 24.2 - Prob. 4CC Ch. 24.2 - Prob. 5CC Ch. 24.2 - Prob. 6CC Ch. 24.4 - Prob. 7CC Ch. 24.4 - Prob. 8CC Ch. 24.5 - Prob. 1LTS Ch. 24.5 - Prob. 9PTS

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Chapter 24 Solutions