For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained. Concept introduction: The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center). The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group . Such as, If the –OH group is located in right side then, the carbohydrate is a D-sugar . If the –OH group is located in left side then, the carbohydrate is a L-sugar . Chiral carbon : Chiral carbon is the one which is bonded to four different molecules or groups. Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows. Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity. If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration . If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration. If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa. The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side. To identify: the given carbohydrate (a) is D or L sugar and the configuration of each chiral center.

Question

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Answer 1

Question

Chapter 24.2, Problem 3CC

(a)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (a) is D or L sugar and the configuration of each chiral center.

(b)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (b) is D or L sugar and the configuration of each chiral center.

(c)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (c) is D or L sugar and the configuration of each chiral center.

(d)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (d) is D or L sugar and the configuration of each chiral center.

(e)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (e) is D or L sugar and the configuration of each chiral center.

(f)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To explain: the trend on the configuration of each chiral center in each given carbohydrates.

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Answer 2

Question

Chapter 24.2, Problem 3CC

(a)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (a) is D or L sugar and the configuration of each chiral center.

(b)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (b) is D or L sugar and the configuration of each chiral center.

(c)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (c) is D or L sugar and the configuration of each chiral center.

(d)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (d) is D or L sugar and the configuration of each chiral center.

(e)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (e) is D or L sugar and the configuration of each chiral center.

(f)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To explain: the trend on the configuration of each chiral center in each given carbohydrates.

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Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 24.2, Problem 3CC

(a)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (a) is D or L sugar and the configuration of each chiral center.

(b)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (b) is D or L sugar and the configuration of each chiral center.

(c)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (c) is D or L sugar and the configuration of each chiral center.

(d)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (d) is D or L sugar and the configuration of each chiral center.

(e)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (e) is D or L sugar and the configuration of each chiral center.

(f)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To explain: the trend on the configuration of each chiral center in each given carbohydrates.

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Answer 4

Question

Chapter 24.2, Problem 3CC

(a)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (a) is D or L sugar and the configuration of each chiral center.

(b)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (b) is D or L sugar and the configuration of each chiral center.

(c)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (c) is D or L sugar and the configuration of each chiral center.

(d)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (d) is D or L sugar and the configuration of each chiral center.

(e)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (e) is D or L sugar and the configuration of each chiral center.

(f)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To explain: the trend on the configuration of each chiral center in each given carbohydrates.

Expert Solution & Answer

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Check out a sample textbook solution

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Answer 5

Chapter 24.2, Problem 3CC

(a)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (a) is D or L sugar and the configuration of each chiral center.

(b)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (b) is D or L sugar and the configuration of each chiral center.

(c)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (c) is D or L sugar and the configuration of each chiral center.

(d)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (d) is D or L sugar and the configuration of each chiral center.

(e)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (e) is D or L sugar and the configuration of each chiral center.

(f)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To explain: the trend on the configuration of each chiral center in each given carbohydrates.

Answer 6

Chapter 24.2, Problem 3CC

(a)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (a) is D or L sugar and the configuration of each chiral center.

Answer 7

Chapter 24.2, Problem 3CC

(a)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (a) is D or L sugar and the configuration of each chiral center.

Answer 8

(b)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (b) is D or L sugar and the configuration of each chiral center.

Answer 9

(b)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (b) is D or L sugar and the configuration of each chiral center.

Answer 10

(c)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (c) is D or L sugar and the configuration of each chiral center.

Answer 11

(c)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (c) is D or L sugar and the configuration of each chiral center.

Answer 12

(d)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (d) is D or L sugar and the configuration of each chiral center.

Answer 13

(d)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (d) is D or L sugar and the configuration of each chiral center.

Answer 14

(e)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (e) is D or L sugar and the configuration of each chiral center.

Answer 15

(e)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To identify: the given carbohydrate (e) is D or L sugar and the configuration of each chiral center.

Answer 16

(f)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To explain: the trend on the configuration of each chiral center in each given carbohydrates.

Answer 17

(f)

Interpretation Introduction

Interpretation:

For each of the given compounds, whether it is D or L sugar should be determined, the configuration of each chiral center should be assigned and the trend on the configuration of each chiral center should be explained.

Concept introduction:

The stereo-descriptor used for carbohydrates is D or L. it is based on the dextrorotatory or levorotatory of smallest carbohydrate glyceraldehyde (1 chiral center).

The stereo-descriptor for other carbohydrates of having more than one chiral center will be evaluated by the location of –OH group (right or left) of farthest chiral carbon from the carbonyl group. Such as,

If the –OH group is located in right side then, the carbohydrate is a D-sugar.

If the –OH group is located in left side then, the carbohydrate is a L-sugar.

Chiral carbon: Chiral carbon is the one which is bonded to four different molecules or groups.

Configuration of a molecule: The configurations of a molecule arise due to the spatial arrangement of atoms. The configuration can be assigned by following CIP rules as follows.

Assign numbering to the groups which are bonded to the chiral carbon based on the molecular weight and electronegativity.

If the sequence of the numbering follows clockwise direction the chiral atom is assigned as R configuration.

If the sequence of the numbering follows anticlockwise direction the chiral atom is assigned as S configuration.

If the least priority group is on horizontal line in the fisher projection, then configuration is inverted to the obtained configuration from the above CIP rule which means R configuration becomes S and vice versa.

The D-configuration is needed not to be dextrorotatory; rather it means the chirality center of farthest from aldo-group is having R-configuration or the –OH group is on right side.

To explain: the trend on the configuration of each chiral center in each given carbohydrates.

Answer 18

Expert Solution & Answer

Answer 19

Expert Solution & Answer

Answer 20

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Answer 21

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