For the four stereo isomeric aldotetroses, the pair of enantiomers and stereo descriptors is needed to be drawn. Concept introduction: Aldoses are monosaccharides, which contains Aldehyde group . The naming of monosaccharides, Prefix : aldo or keto indicates whether the monosaccharide is containing aldehyde or ketone group. Suffix: ose indicates the carbohydrates Root word: indicate the number of carbons. The stereo-descriptor used for monosaccharides is D or L. it is based on the dextrorotatory glyceraldehyde or levorotatory glyceraldehyde. 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 . Enantiomers are non-super imposable mirror images of each other. To determine: the structures of pair of enantiomers of stereo isomeric aldotetroses.

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Answer 1

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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 24.2, Problem 6CC

(a)

Interpretation Introduction

Interpretation:

For the four stereo isomeric aldotetroses, the pair of enantiomers and stereo descriptors is needed to be drawn.

Concept introduction:

Aldoses are monosaccharides, which contains Aldehyde group.

The naming of monosaccharides,

Prefix: aldo or keto indicates whether the monosaccharide is containing aldehyde or ketone group.

Suffix: ose indicates the carbohydrates

Root word: indicate the number of carbons.

The stereo-descriptor used for monosaccharides is D or L. it is based on the dextrorotatory glyceraldehyde or levorotatory glyceraldehyde.

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.

Enantiomers are non-super imposable mirror images of each other.

To determine: the structures of pair of enantiomers of stereo isomeric aldotetroses.

(b)

Interpretation Introduction

Interpretation:

For the four stereo isomeric aldotetroses, the pair of enantiomers and stereo descriptors is needed to be drawn.

Concept introduction:

Aldoses are monosaccharides, which contains Aldehyde group.

The naming of monosaccharides,

Prefix: aldo or keto indicates whether the monosaccharide is containing aldehyde or ketone group.

Suffix: ose indicates the carbohydrates

Root word: indicate the number of carbons.

The stereo-descriptor used for monosaccharides is D or L. it is based on the dextrorotatory glyceraldehyde or levorotatory glyceraldehyde.

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.

Enantiomers are non-super imposable mirror images of each other.

To identify: the D sugar and L sugar from the four structures of stereo isomeric aldotetroses.

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Students have asked these similar questions

A. B. b. Now consider the two bicyclic molecules A. and B. Note that A. is a dianion and B. is a neutral molecule. One of these molecules is a highly reactive compound first characterized in frozen noble gas matrices, that self-reacts rapidly at temperatures above liquid nitrogen temperature. The other compound was isolated at room temperature in the early 1960s, and is a stable ligand used in organometallic chemistry. Which molecule is the more stable molecule, and why?

Where are the chiral centers in this molecule? Also is this compound meso yes or no?

PLEASE HELP! URGENT!

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 24.2, Problem 6CC

(a)

Interpretation Introduction

Interpretation:

For the four stereo isomeric aldotetroses, the pair of enantiomers and stereo descriptors is needed to be drawn.

Concept introduction:

Aldoses are monosaccharides, which contains Aldehyde group.

The naming of monosaccharides,

Prefix: aldo or keto indicates whether the monosaccharide is containing aldehyde or ketone group.

Suffix: ose indicates the carbohydrates

Root word: indicate the number of carbons.

The stereo-descriptor used for monosaccharides is D or L. it is based on the dextrorotatory glyceraldehyde or levorotatory glyceraldehyde.

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.

Enantiomers are non-super imposable mirror images of each other.

To determine: the structures of pair of enantiomers of stereo isomeric aldotetroses.

(b)

Interpretation Introduction

Interpretation:

For the four stereo isomeric aldotetroses, the pair of enantiomers and stereo descriptors is needed to be drawn.

Concept introduction:

Aldoses are monosaccharides, which contains Aldehyde group.

The naming of monosaccharides,

Prefix: aldo or keto indicates whether the monosaccharide is containing aldehyde or ketone group.

Suffix: ose indicates the carbohydrates

Root word: indicate the number of carbons.

The stereo-descriptor used for monosaccharides is D or L. it is based on the dextrorotatory glyceraldehyde or levorotatory glyceraldehyde.

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.

Enantiomers are non-super imposable mirror images of each other.

To identify: the D sugar and L sugar from the four structures of stereo isomeric aldotetroses.

Expert Solution & Answer

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Check out a sample textbook solution

See solution

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 24.2, Problem 6CC

(a)

Interpretation Introduction

Interpretation:

For the four stereo isomeric aldotetroses, the pair of enantiomers and stereo descriptors is needed to be drawn.

Concept introduction:

Aldoses are monosaccharides, which contains Aldehyde group.

The naming of monosaccharides,

Prefix: aldo or keto indicates whether the monosaccharide is containing aldehyde or ketone group.

Suffix: ose indicates the carbohydrates

Root word: indicate the number of carbons.

The stereo-descriptor used for monosaccharides is D or L. it is based on the dextrorotatory glyceraldehyde or levorotatory glyceraldehyde.

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.

Enantiomers are non-super imposable mirror images of each other.

To determine: the structures of pair of enantiomers of stereo isomeric aldotetroses.

(b)

Interpretation Introduction

Interpretation:

For the four stereo isomeric aldotetroses, the pair of enantiomers and stereo descriptors is needed to be drawn.

Concept introduction:

Aldoses are monosaccharides, which contains Aldehyde group.

The naming of monosaccharides,

Prefix: aldo or keto indicates whether the monosaccharide is containing aldehyde or ketone group.

Suffix: ose indicates the carbohydrates

Root word: indicate the number of carbons.

The stereo-descriptor used for monosaccharides is D or L. it is based on the dextrorotatory glyceraldehyde or levorotatory glyceraldehyde.

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.

Enantiomers are non-super imposable mirror images of each other.

To identify: the D sugar and L sugar from the four structures of stereo isomeric aldotetroses.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

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 24.2, Problem 6CC

(a)

Interpretation Introduction