(a) Interpretation: The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed. Concept Introduction: A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions. The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left. All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

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Answer 1

Question

Chapter 20, Problem 20.27P

Interpretation Introduction

(a)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

Interpretation Introduction

(b)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

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Choose the Lewis structure for the compound below: H2CCHOCH2CH(CH3)2 HH H :d H H H C. Η H H HH H H H H. H H H HH H H H H H- H H H C-H H H HHHH

Each of the highlighted carbon atoms is connected to hydrogen atoms.

く Complete the reaction in the drawing area below by adding the major products to the right-hand side. If there won't be any products, because nothing will happen under these reaction conditions, check the box under the drawing area instead. Note: if the products contain one or more pairs of enantiomers, don't worry about drawing each enantiomer with dash and wedge bonds. Just draw one molecule to represent each pair of enantiomers, using line bonds at the chiral center. More... No reaction. Explanation Check O + G 1. Na O Me Click and drag to start drawing a structure. 2. H + 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility 000 Ar P

Answer 2

Question

Chapter 20, Problem 20.27P

Interpretation Introduction

(a)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

Interpretation Introduction

(b)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

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Answer 3

Question

Chapter 20, Problem 20.27P

Interpretation Introduction

(a)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

Interpretation Introduction

(b)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

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Answer 4

Question

Chapter 20, Problem 20.27P

Interpretation Introduction

(a)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

Interpretation Introduction

(b)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

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Answer 5

Chapter 20, Problem 20.27P

Interpretation Introduction

(a)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

Interpretation Introduction

(b)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

Answer 6

Chapter 20, Problem 20.27P

Interpretation Introduction

(a)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

Answer 7

Chapter 20, Problem 20.27P

Interpretation Introduction

(a)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The given chair forms should be converted into an open-chain form and to Fischer projections. Also, name the monosaccharide so formed.

Concept Introduction:

A chair form is most stable conformation of cyclic hydrocarbon.Here, hydrogens are at axial positions and hydroxyl groups are at equilitorial positions.

The Fischer projection is two dimensional representation of the three-dimensional projection. It is used to differentiate between D and L molecules. In the D configuration, the carbon next to the last has hydrogen on the left and hydroxyl group on the right whereas in L configuration, the hydrogen is on the right a hydroxyl group on the left.

All the horizontal bonds in the Fischer projection are directed towards the viewer and vertical bonds are directed away from the viewer.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 20.1 - Prob. 20.1P Ch. 20.2 - Prob. 20.2P Ch. 20.2 - Prob. 20.3P Ch. 20.3 - Prob. 20.4P Ch. 20.4 - Prob. 20.5P Ch. 20 - Prob. 20.6P Ch. 20 - Prob. 20.7P Ch. 20 - Prob. 20.8P Ch. 20 - Prob. 20.9P Ch. 20 - Prob. 20.10P

Solution Summary: The author explains that a chair form is most stable conformation of cyclic hydrocarbon. The Fischer projection is two dimensional representation of the three-dimensional projection.

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