The chirality centers in aldotetrose and ketopentose are to be calculated and the stereoisomers for each general case are to be determined. Concept Introduction: Carbohydrates are categorized mainly as monosaccharides, disaccharides, and polysaccharides. Monosaccharides are single sugar units, mainly glucose and fructose, disaccharides are two sugar units, such as sucrose, and polysaccharides are more than two sugar units, such as starch and cellulose. Monosaccharides containing 3-carbon atoms are called triose , 4-carbon atoms called tetrose, 5-carbon atoms called pentose, and so on. In chiral molecules, carbon atom having four nonidentical substituent groups is called the chirality center of that molecule. Chirality center may also be called stereocenter, which signifies any point in the molecule where the interchanging of any two groups may lead to stereoisomers. The carbon of a carbohydrate can be considered as chiral when the carbon has all four different substituents attached to it. The stereoisomers are calculated as follows: Number of stereoisomers = 2 n Here, n is the number of chiral centers.

Question

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Answer 1

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 22, Problem 1PP

Interpretation Introduction

Interpretation:

The chirality centers in aldotetrose and ketopentose are to be calculated and the stereoisomers for each general case are to be determined.

Concept Introduction:

Carbohydrates are categorized mainly as monosaccharides, disaccharides, and polysaccharides. Monosaccharides are single sugar units, mainly glucose and fructose, disaccharides are two sugar units, such as sucrose, and polysaccharides are more than two sugar units, such as starch and cellulose.

Monosaccharides containing 3-carbon atoms are called triose, 4-carbon atoms called tetrose, 5-carbon atoms called pentose, and so on.

In chiral molecules, carbon atom having four nonidentical substituent groups is called the chirality center of that molecule. Chirality center may also be called stereocenter, which signifies any point in the molecule where the interchanging of any two groups may lead to stereoisomers. The carbon of a carbohydrate can be considered as chiral when the carbon has all four different substituents attached to it.

The stereoisomers are calculated as follows:

Number of stereoisomers=2n

Here, n is the number of chiral centers.

Expert Solution & Answer

Answer to Problem 1PP

Solution:

a) Two

b) Two

c) Four

Explanation of Solution

a) The aldotetrose

A monosaccharide containing four carbon atoms is called a tetrose. An aldotetrose is a monosaccharide that contains aldehyde group.

The structure of aldotetrose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 1

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 2

Hence, an aldotetrose has two chirality centers.

b) The ketopentose

A monosaccharide containing five carbon atoms is called a pentose. A pentose containing a keto group is called a ketopentose.

The structure of ketopentose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 3

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 4

Hence, a ketopentose has two chirality centers.

c) The number of stereoisomers that will be expected from each general structure

Stereoisomers of a molecule have the same molecular formula, but different arrangement of atoms in space. Stereoisomers are different from enantiomers as they are not mirror images of each other, while enantiomers are mirror images of one another.

The compounds aldotetrose and ketopentose have two sets of enantiomers. The number of stereoisomers is calculated as:

Number of stereoisomers=2n

Substitute 2 for n in the above expression as follows:

Number of stereoisomers =22=4

Hence, they will have four stereoisomers for each general structure.

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Answer 2

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 22, Problem 1PP

Interpretation Introduction

Interpretation:

The chirality centers in aldotetrose and ketopentose are to be calculated and the stereoisomers for each general case are to be determined.

Concept Introduction:

Carbohydrates are categorized mainly as monosaccharides, disaccharides, and polysaccharides. Monosaccharides are single sugar units, mainly glucose and fructose, disaccharides are two sugar units, such as sucrose, and polysaccharides are more than two sugar units, such as starch and cellulose.

Monosaccharides containing 3-carbon atoms are called triose, 4-carbon atoms called tetrose, 5-carbon atoms called pentose, and so on.

In chiral molecules, carbon atom having four nonidentical substituent groups is called the chirality center of that molecule. Chirality center may also be called stereocenter, which signifies any point in the molecule where the interchanging of any two groups may lead to stereoisomers. The carbon of a carbohydrate can be considered as chiral when the carbon has all four different substituents attached to it.

The stereoisomers are calculated as follows:

Number of stereoisomers=2n

Here, n is the number of chiral centers.

Expert Solution & Answer

Answer to Problem 1PP

Solution:

a) Two

b) Two

c) Four

Explanation of Solution

a) The aldotetrose

A monosaccharide containing four carbon atoms is called a tetrose. An aldotetrose is a monosaccharide that contains aldehyde group.

The structure of aldotetrose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 1

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 2

Hence, an aldotetrose has two chirality centers.

b) The ketopentose

A monosaccharide containing five carbon atoms is called a pentose. A pentose containing a keto group is called a ketopentose.

The structure of ketopentose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 3

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 4

Hence, a ketopentose has two chirality centers.

c) The number of stereoisomers that will be expected from each general structure

Stereoisomers of a molecule have the same molecular formula, but different arrangement of atoms in space. Stereoisomers are different from enantiomers as they are not mirror images of each other, while enantiomers are mirror images of one another.

The compounds aldotetrose and ketopentose have two sets of enantiomers. The number of stereoisomers is calculated as:

Number of stereoisomers=2n

Substitute 2 for n in the above expression as follows:

Number of stereoisomers =22=4

Hence, they will have four stereoisomers for each general structure.

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Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 22, Problem 1PP

Interpretation Introduction

Interpretation:

The chirality centers in aldotetrose and ketopentose are to be calculated and the stereoisomers for each general case are to be determined.

Concept Introduction:

Carbohydrates are categorized mainly as monosaccharides, disaccharides, and polysaccharides. Monosaccharides are single sugar units, mainly glucose and fructose, disaccharides are two sugar units, such as sucrose, and polysaccharides are more than two sugar units, such as starch and cellulose.

Monosaccharides containing 3-carbon atoms are called triose, 4-carbon atoms called tetrose, 5-carbon atoms called pentose, and so on.

In chiral molecules, carbon atom having four nonidentical substituent groups is called the chirality center of that molecule. Chirality center may also be called stereocenter, which signifies any point in the molecule where the interchanging of any two groups may lead to stereoisomers. The carbon of a carbohydrate can be considered as chiral when the carbon has all four different substituents attached to it.

The stereoisomers are calculated as follows:

Number of stereoisomers=2n

Here, n is the number of chiral centers.

Expert Solution & Answer

Answer to Problem 1PP

Solution:

a) Two

b) Two

c) Four

Explanation of Solution

a) The aldotetrose

A monosaccharide containing four carbon atoms is called a tetrose. An aldotetrose is a monosaccharide that contains aldehyde group.

The structure of aldotetrose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 1

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 2

Hence, an aldotetrose has two chirality centers.

b) The ketopentose

A monosaccharide containing five carbon atoms is called a pentose. A pentose containing a keto group is called a ketopentose.

The structure of ketopentose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 3

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 4

Hence, a ketopentose has two chirality centers.

c) The number of stereoisomers that will be expected from each general structure

Stereoisomers of a molecule have the same molecular formula, but different arrangement of atoms in space. Stereoisomers are different from enantiomers as they are not mirror images of each other, while enantiomers are mirror images of one another.

The compounds aldotetrose and ketopentose have two sets of enantiomers. The number of stereoisomers is calculated as:

Number of stereoisomers=2n

Substitute 2 for n in the above expression as follows:

Number of stereoisomers =22=4

Hence, they will have four stereoisomers for each general structure.

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Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 22, Problem 1PP

Interpretation Introduction

Interpretation:

The chirality centers in aldotetrose and ketopentose are to be calculated and the stereoisomers for each general case are to be determined.

Concept Introduction:

Carbohydrates are categorized mainly as monosaccharides, disaccharides, and polysaccharides. Monosaccharides are single sugar units, mainly glucose and fructose, disaccharides are two sugar units, such as sucrose, and polysaccharides are more than two sugar units, such as starch and cellulose.

Monosaccharides containing 3-carbon atoms are called triose, 4-carbon atoms called tetrose, 5-carbon atoms called pentose, and so on.

In chiral molecules, carbon atom having four nonidentical substituent groups is called the chirality center of that molecule. Chirality center may also be called stereocenter, which signifies any point in the molecule where the interchanging of any two groups may lead to stereoisomers. The carbon of a carbohydrate can be considered as chiral when the carbon has all four different substituents attached to it.

The stereoisomers are calculated as follows:

Number of stereoisomers=2n

Here, n is the number of chiral centers.

Expert Solution & Answer

Answer to Problem 1PP

Solution:

a) Two

b) Two

c) Four

Explanation of Solution

a) The aldotetrose

A monosaccharide containing four carbon atoms is called a tetrose. An aldotetrose is a monosaccharide that contains aldehyde group.

The structure of aldotetrose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 1

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 2

Hence, an aldotetrose has two chirality centers.

b) The ketopentose

A monosaccharide containing five carbon atoms is called a pentose. A pentose containing a keto group is called a ketopentose.

The structure of ketopentose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 3

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 4

Hence, a ketopentose has two chirality centers.

c) The number of stereoisomers that will be expected from each general structure

Stereoisomers of a molecule have the same molecular formula, but different arrangement of atoms in space. Stereoisomers are different from enantiomers as they are not mirror images of each other, while enantiomers are mirror images of one another.

The compounds aldotetrose and ketopentose have two sets of enantiomers. The number of stereoisomers is calculated as:

Number of stereoisomers=2n

Substitute 2 for n in the above expression as follows:

Number of stereoisomers =22=4

Hence, they will have four stereoisomers for each general structure.

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Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!

Answer 5

Chapter 22, Problem 1PP

Interpretation Introduction

Interpretation:

The chirality centers in aldotetrose and ketopentose are to be calculated and the stereoisomers for each general case are to be determined.

Concept Introduction:

Carbohydrates are categorized mainly as monosaccharides, disaccharides, and polysaccharides. Monosaccharides are single sugar units, mainly glucose and fructose, disaccharides are two sugar units, such as sucrose, and polysaccharides are more than two sugar units, such as starch and cellulose.

Monosaccharides containing 3-carbon atoms are called triose, 4-carbon atoms called tetrose, 5-carbon atoms called pentose, and so on.

In chiral molecules, carbon atom having four nonidentical substituent groups is called the chirality center of that molecule. Chirality center may also be called stereocenter, which signifies any point in the molecule where the interchanging of any two groups may lead to stereoisomers. The carbon of a carbohydrate can be considered as chiral when the carbon has all four different substituents attached to it.

The stereoisomers are calculated as follows:

Number of stereoisomers=2n

Here, n is the number of chiral centers.

Expert Solution & Answer

Answer to Problem 1PP

Solution:

a) Two

b) Two

c) Four

Explanation of Solution

a) The aldotetrose

A monosaccharide containing four carbon atoms is called a tetrose. An aldotetrose is a monosaccharide that contains aldehyde group.

The structure of aldotetrose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 1

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 2

Hence, an aldotetrose has two chirality centers.

b) The ketopentose

A monosaccharide containing five carbon atoms is called a pentose. A pentose containing a keto group is called a ketopentose.

The structure of ketopentose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 3

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 4

Hence, a ketopentose has two chirality centers.

c) The number of stereoisomers that will be expected from each general structure

Stereoisomers of a molecule have the same molecular formula, but different arrangement of atoms in space. Stereoisomers are different from enantiomers as they are not mirror images of each other, while enantiomers are mirror images of one another.

The compounds aldotetrose and ketopentose have two sets of enantiomers. The number of stereoisomers is calculated as:

Number of stereoisomers=2n

Substitute 2 for n in the above expression as follows:

Number of stereoisomers =22=4

Hence, they will have four stereoisomers for each general structure.

Answer 6

Chapter 22, Problem 1PP

Interpretation Introduction

Interpretation:

The chirality centers in aldotetrose and ketopentose are to be calculated and the stereoisomers for each general case are to be determined.

Concept Introduction:

Carbohydrates are categorized mainly as monosaccharides, disaccharides, and polysaccharides. Monosaccharides are single sugar units, mainly glucose and fructose, disaccharides are two sugar units, such as sucrose, and polysaccharides are more than two sugar units, such as starch and cellulose.

Monosaccharides containing 3-carbon atoms are called triose, 4-carbon atoms called tetrose, 5-carbon atoms called pentose, and so on.

In chiral molecules, carbon atom having four nonidentical substituent groups is called the chirality center of that molecule. Chirality center may also be called stereocenter, which signifies any point in the molecule where the interchanging of any two groups may lead to stereoisomers. The carbon of a carbohydrate can be considered as chiral when the carbon has all four different substituents attached to it.

The stereoisomers are calculated as follows:

Number of stereoisomers=2n

Here, n is the number of chiral centers.

Expert Solution & Answer

Answer to Problem 1PP

Solution:

a) Two

b) Two

c) Four

Explanation of Solution

a) The aldotetrose

A monosaccharide containing four carbon atoms is called a tetrose. An aldotetrose is a monosaccharide that contains aldehyde group.

The structure of aldotetrose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 1

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 2

Hence, an aldotetrose has two chirality centers.

b) The ketopentose

A monosaccharide containing five carbon atoms is called a pentose. A pentose containing a keto group is called a ketopentose.

The structure of ketopentose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 3

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 4

Hence, a ketopentose has two chirality centers.

c) The number of stereoisomers that will be expected from each general structure

Stereoisomers of a molecule have the same molecular formula, but different arrangement of atoms in space. Stereoisomers are different from enantiomers as they are not mirror images of each other, while enantiomers are mirror images of one another.

The compounds aldotetrose and ketopentose have two sets of enantiomers. The number of stereoisomers is calculated as:

Number of stereoisomers=2n

Substitute 2 for n in the above expression as follows:

Number of stereoisomers =22=4

Hence, they will have four stereoisomers for each general structure.

Answer 7

Chapter 22, Problem 1PP

Interpretation Introduction

Interpretation:

The chirality centers in aldotetrose and ketopentose are to be calculated and the stereoisomers for each general case are to be determined.

Concept Introduction:

Carbohydrates are categorized mainly as monosaccharides, disaccharides, and polysaccharides. Monosaccharides are single sugar units, mainly glucose and fructose, disaccharides are two sugar units, such as sucrose, and polysaccharides are more than two sugar units, such as starch and cellulose.

Monosaccharides containing 3-carbon atoms are called triose, 4-carbon atoms called tetrose, 5-carbon atoms called pentose, and so on.

In chiral molecules, carbon atom having four nonidentical substituent groups is called the chirality center of that molecule. Chirality center may also be called stereocenter, which signifies any point in the molecule where the interchanging of any two groups may lead to stereoisomers. The carbon of a carbohydrate can be considered as chiral when the carbon has all four different substituents attached to it.

The stereoisomers are calculated as follows:

Number of stereoisomers=2n

Here, n is the number of chiral centers.

Answer 8

Expert Solution & Answer

Answer to Problem 1PP

Solution:

a) Two

b) Two

c) Four

Answer 9

Expert Solution & Answer

Answer 10

Expert Solution & Answer

Answer 11

Explanation of Solution

a) The aldotetrose

A monosaccharide containing four carbon atoms is called a tetrose. An aldotetrose is a monosaccharide that contains aldehyde group.

The structure of aldotetrose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 1

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 2

Hence, an aldotetrose has two chirality centers.

b) The ketopentose

A monosaccharide containing five carbon atoms is called a pentose. A pentose containing a keto group is called a ketopentose.

The structure of ketopentose is as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 3

The carbon atom attached to four different groups is chiral carbon. The chiral center in ketopentose is marked by * as follows:

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS, Chapter 22, Problem 1PP , additional homework tip 4

Hence, a ketopentose has two chirality centers.

c) The number of stereoisomers that will be expected from each general structure

Stereoisomers of a molecule have the same molecular formula, but different arrangement of atoms in space. Stereoisomers are different from enantiomers as they are not mirror images of each other, while enantiomers are mirror images of one another.

The compounds aldotetrose and ketopentose have two sets of enantiomers. The number of stereoisomers is calculated as:

Number of stereoisomers=2n

Substitute 2 for n in the above expression as follows:

Number of stereoisomers =22=4

Hence, they will have four stereoisomers for each general structure.

Answer 12

Ch. 22 - Prob. 1PP Ch. 22 - Prob. 2PP Ch. 22 - Prob. 3PP Ch. 22 - Prob. 4PP Ch. 22 - Prob. 5PP Ch. 22 - Prob. 6PP Ch. 22 - Prob. 7PP Ch. 22 - Prob. 8PP Ch. 22 - Practice Problem 22.9 What products would you...Ch. 22 - Prob. 10PP

Concept explainers

Answer to Problem 1PP

Explanation of Solution

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Chapter 22 Solutions