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.

Question

Want to see the full answer?

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 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

Students have asked these similar questions

Draw the structure of the pound in the provided CO as a 300-1200 37(2), 11 ( 110, and 2.5 (20

Please help me with # 4 and 5. Thanks in advance!

A small artisanal cheesemaker is testing the acidity of their milk before it coagulates. During fermentation, bacteria produce lactic acid (K₁ = 1.4 x 104), a weak acid that helps to curdle the milk and develop flavor. The cheesemaker has measured that the developing mixture contains lactic acid at an initial concentration of 0.025 M. Your task is to calculate the pH of this mixture and determine whether it meets the required acidity for proper cheese development. To achieve the best flavor, texture and reduce/control microbial growth, the pH range needs to be between pH 4.6 and 5.0. Assumptions: Lactic acid is a monoprotic acid H H :0:0: H-C-C H :0: O-H Figure 1: Lewis Structure for Lactic Acid For simplicity, you can use the generic formula HA to represent the acid You can assume lactic acid dissociation is in water as milk is mostly water. Temperature is 25°C 1. Write the K, expression for the dissociation of lactic acid in the space provided. Do not forget to include state symbols.…

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

Want to see the full answer?

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