(a) Interpretation: The Fischer projection formula of L-lyxose is to be drawn. Concept introduction: Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

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Answer 1

Question

Chapter 5, Problem 5.66P

Interpretation Introduction

(a)

Interpretation:

The Fischer projection formula of L-lyxose is to be drawn.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

Interpretation Introduction

(b)

Interpretation:

To be drawing the Fischer projection of l-talose.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

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Students have asked these similar questions

Draw the Fischer projection of (a) L-lyxose and (b) L-talose.

Draw a chair conformation for a β anomer of a disaccharide in which the two units ofD-glucopyranose are joined by an α-1,6-glycosidic bond.

Draw a chair conformation for the b-anomer of a disaccharide in which two units of d-glucopyranose are joined by an a-1,6-glycosidic bond.

Answer 2

Question

Chapter 5, Problem 5.66P

Interpretation Introduction

(a)

Interpretation:

The Fischer projection formula of L-lyxose is to be drawn.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

Interpretation Introduction

(b)

Interpretation:

To be drawing the Fischer projection of l-talose.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

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Answer 3

Question

Chapter 5, Problem 5.66P

Interpretation Introduction

(a)

Interpretation:

The Fischer projection formula of L-lyxose is to be drawn.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

Interpretation Introduction

(b)

Interpretation:

To be drawing the Fischer projection of l-talose.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

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Answer 4

Question

Chapter 5, Problem 5.66P

Interpretation Introduction

(a)

Interpretation:

The Fischer projection formula of L-lyxose is to be drawn.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

Interpretation Introduction

(b)

Interpretation:

To be drawing the Fischer projection of l-talose.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

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Answer 5

Chapter 5, Problem 5.66P

Interpretation Introduction

(a)

Interpretation:

The Fischer projection formula of L-lyxose is to be drawn.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

Interpretation Introduction

(b)

Interpretation:

To be drawing the Fischer projection of l-talose.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

Answer 6

Chapter 5, Problem 5.66P

Interpretation Introduction

(a)

Interpretation:

The Fischer projection formula of L-lyxose is to be drawn.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

Answer 7

Chapter 5, Problem 5.66P

Interpretation Introduction

(a)

Interpretation:

The Fischer projection formula of L-lyxose is to be drawn.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

Answer 8

Interpretation Introduction

(b)

Interpretation:

To be drawing the Fischer projection of l-talose.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

Answer 9

Interpretation Introduction

(b)

Interpretation:

To be drawing the Fischer projection of l-talose.

Concept introduction:

Fischer projections are shorthand notations used to represent the configurations about asymmetric carbons in a molecule, particularly sugars. The molecule is drawn with the carbonyl functional group at the top. Perpendicular intersecting lines represent a carbon atom typically a chiral center. Horizontal bonds point toward the viewer, whereas vertical bonds point away from the viewer. In Fischer projection of L form, the OH group of the highest numbered asymmetric carbon is on the left side of the projection.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 5 - Prob. 5.1P Ch. 5 - Prob. 5.2P Ch. 5 - Prob. 5.3P Ch. 5 - Prob. 5.4P Ch. 5 - Prob. 5.5P Ch. 5 - Prob. 5.6P Ch. 5 - Prob. 5.7P Ch. 5 - Prob. 5.8P Ch. 5 - Prob. 5.9P Ch. 5 - Prob. 5.10P

Solution Summary: The author explains the Fischer projection formula of L-lyxose. The molecule is drawn with the carbonyl functional group at the top.

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Chapter 5 Solutions