Organic Chemistry, Binder Ready Version
Organic Chemistry, Binder Ready Version
2nd Edition
ISBN: 9781118454312
Author: David R. Klein
Publisher: WILEY
Question
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Chapter 24, Problem 42PP

(a)

Interpretation Introduction

Interpretation:

The given molecule is D or L should be identified.

Concept introduction:

Monosaccharides: (single sugar unit) simple sugars units are the most basic units of carbohydrates.

Structure and nomenclature: Monosaccharide has this chemical formula: Cx(H2O)y

Monosaccharides can be classified by the number x of carbon atoms. If they contain three carbon atom and is called triose. If they contain four carbon and is called tetrose, if they contain five carbon and is called pentose, if they contain six carbon and is called hexose and so on.

Aldose:  A monosaccharide in which carbon serves as a backbone and contains an aldehyde group at the beginning.

Ketose: A ketose is a simple sugar unit (monosaccharide) containing one ketone group per molecule.

D and L enantiomers: L isomers have the hydroxyl group attached to the left side of the asymmetric carbon furthest from the carbonyl.

R isomers have the hydroxyl group attached to the right side of the asymmetric carbon furthest from the carbonyl.

To find: Type of enantiomers.

(a)

Expert Solution
Check Mark

Answer to Problem 42PP

Answer

The given compound is D-aldotetrose (a).

Organic Chemistry, Binder Ready Version, Chapter 24, Problem 42PP , additional homework tip  1

Explanation of Solution

The OH group connected to C3 is pointing to the right side, so it is called as D-sugar. The functional group at Cl atom is an aldehyde group, so the compound is an aldose. Finally, the compound has four carbon atoms in a molecule, so it is a tetrose. The given compound is a D-aldotetrose.

(b)

Interpretation Introduction

Interpretation:

The given molecule is D or L should be identified.

Concept introduction:

Monosaccharides: (single sugar unit) simple sugars units are the most basic units of carbohydrates.

Structure and nomenclature: Monosaccharide has this chemical formula: Cx(H2O)y

Monosaccharides can be classified by the number x of carbon atoms. If they contain three carbon atom and is called triose. If they contain four carbon and is called tetrose, if they contain five carbon and is called pentose, if they contain six carbon and is called hexose and so on.

Aldose:  A monosaccharide in which carbon serves as a backbone and contains an aldehyde group at the beginning.

Ketose: A ketose is a simple sugar unit (monosaccharide) containing one ketone group per molecule.

D and L enantiomers: L isomers have the hydroxyl group attached to the left side of the asymmetric carbon furthest from the carbonyl.

R isomers have the hydroxyl group attached to the right side of the asymmetric carbon furthest from the carbonyl.

To find: Type of enantiomers.

(b)

Expert Solution
Check Mark

Answer to Problem 42PP

Answer

The given compound is L-aldopentose (b).

Organic Chemistry, Binder Ready Version, Chapter 24, Problem 42PP , additional homework tip  2

Explanation of Solution

The given compound is L-aldopentose.

Organic Chemistry, Binder Ready Version, Chapter 24, Problem 42PP , additional homework tip  3

The OH group connected to C4 is pointing to the left side, so it is called as L-sugar. The functional group at Cl is an aldehyde group, so the compound is an aldose. Finally, the compound has five carbon atoms, so it is a pentose. The given compound is an L-aldopentose

(c)

Interpretation Introduction

Interpretation:

The given molecule is D or L should be identified.

Concept introduction:

Monosaccharides: (single sugar unit) simple sugars units are the most basic units of carbohydrates.

Structure and nomenclature: Monosaccharide has this chemical formula: Cx(H2O)y

Monosaccharides can be classified by the number x of carbon atoms. If they contain three carbon atom and is called triose. If they contain four carbon and is called tetrose, if they contain five carbon and is called pentose, if they contain six carbon and is called hexose and so on.

Aldose:  A monosaccharide in which carbon serves as a backbone and contains an aldehyde group at the beginning.

Ketose: A ketose is a simple sugar unit (monosaccharide) containing one ketone group per molecule.

D and L enantiomers: L isomers have the hydroxyl group attached to the left side of the asymmetric carbon furthest from the carbonyl.

R isomers have the hydroxyl group attached to the right side of the asymmetric carbon furthest from the carbonyl.

To find: Type of enantiomers.

(c)

Expert Solution
Check Mark

Answer to Problem 42PP

Answer

The given compound is D-aldopentose (c).

Organic Chemistry, Binder Ready Version, Chapter 24, Problem 42PP , additional homework tip  4

Explanation of Solution

The given compound is D-aldopentose.

Organic Chemistry, Binder Ready Version, Chapter 24, Problem 42PP , additional homework tip  5

The OH group connected to C4 is pointing to the right side, so this is a D-sugar. The functional group at Cl is an aldehyde group, so the compound is an aldose. Finally, the compound has five carbon atoms, so it is a pentose. The given compound is a D-aldopentose.

(d)

Interpretation Introduction

Interpretation:

The given molecule is D or L should be identified.

Concept introduction:

Monosaccharides: (single sugar unit) simple sugars units are the most basic units of carbohydrates.

Structure and nomenclature: Monosaccharide has this chemical formula: Cx(H2O)y

Monosaccharides can be classified by the number x of carbon atoms. If they contain three carbon atom and is called triose. If they contain four carbon and is called tetrose, if they contain five carbon and is called pentose, if they contain six carbon and is called hexose and so on.

Aldose:  A monosaccharide in which carbon serves as a backbone and contains an aldehyde group at the beginning.

Ketose: A ketose is a simple sugar unit (monosaccharide) containing one ketone group per molecule.

D and L enantiomers: L isomers have the hydroxyl group attached to the left side of the asymmetric carbon furthest from the carbonyl.

R isomers have the hydroxyl group attached to the right side of the asymmetric carbon furthest from the carbonyl.

To find: Type of enantiomers.

(d)

Expert Solution
Check Mark

Answer to Problem 42PP

Answer

The given compound is D-aldohexose (d).

Organic Chemistry, Binder Ready Version, Chapter 24, Problem 42PP , additional homework tip  6

Explanation of Solution

The given compound is D-aldohexose.

Organic Chemistry, Binder Ready Version, Chapter 24, Problem 42PP , additional homework tip  7

The OH group connected to C5 is pointing to the right side, so this is a D-sugar. The functional group at Cl is an aldehyde group, so the compound is an aldose. Finally, the compound has six carbon atoms, so it is called as a hexose. The given compound is a D-aldohexose

(e)

Interpretation Introduction

Interpretation:

The given molecule is D or L should be identified.

Concept introduction:

Monosaccharides: (single sugar unit) simple sugars units are the most basic units of carbohydrates.

Structure and nomenclature: Monosaccharide has this chemical formula: Cx(H2O)y

Monosaccharides can be classified by the number x of carbon atoms. If they contain three carbon atom and is called triose. If they contain four carbon and is called tetrose, if they contain five carbon and is called pentose, if they contain six carbon and is called hexose and so on.

Aldose:  A monosaccharide in which carbon serves as a backbone and contains an aldehyde group at the beginning.

Ketose: A ketose is a simple sugar unit (monosaccharide) containing one ketone group per molecule.

D and L enantiomers: L isomers have the hydroxyl group attached to the left side of the asymmetric carbon furthest from the carbonyl.

R isomers have the hydroxyl group attached to the right side of the asymmetric carbon furthest from the carbonyl.

To find: Type of enantiomers.

(e)

Expert Solution
Check Mark

Answer to Problem 42PP

Answer

The given compound is D-ketopentose (e).

Organic Chemistry, Binder Ready Version, Chapter 24, Problem 42PP , additional homework tip  8

Explanation of Solution

The given compound is D-ketopentose.

Organic Chemistry, Binder Ready Version, Chapter 24, Problem 42PP , additional homework tip  9

The OH group connected to C4 is pointing to the right side, so this is a D-sugar. The functional group at C2 is a ketone group, so the compound is a ketose. Finally, the compound has five carbon atoms, so it is a pentose. The given compound is a D-ketopentose.

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Chapter 24 Solutions

Organic Chemistry, Binder Ready Version

Ch. 24.5 - Prob. 10ATSCh. 24.5 - Prob. 11ATSCh. 24.5 - Prob. 2LTSCh. 24.5 - Prob. 12LTSCh. 24.5 - Prob. 13ATSCh. 24.5 - Prob. 14ATSCh. 24.5 - Prob. 15ATSCh. 24.5 - Prob. 3LTSCh. 24.5 - Prob. 16PTSCh. 24.5 - Prob. 17ATSCh. 24.5 - Prob. 18ATSCh. 24.5 - Prob. 19CCCh. 24.5 - Prob. 20CCCh. 24.5 - Prob. 21CCCh. 24.5 - Prob. 22CCCh. 24.6 - Prob. 23CCCh. 24.6 - Prob. 24CCCh. 24.6 - Prob. 25CCCh. 24.6 - Prob. 26CCCh. 24.6 - Prob. 27CCCh. 24.6 - Prob. 28CCCh. 24.6 - Prob. 29CCCh. 24.6 - Prob. 30CCCh. 24.6 - Prob. 4LTSCh. 24.6 - Prob. 31PTSCh. 24.6 - Prob. 32ATSCh. 24.6 - Prob. 33ATSCh. 24.6 - Prob. 34CCCh. 24.6 - Prob. 35CCCh. 24.6 - Prob. 36CCCh. 24.6 - Prob. 37CCCh. 24.6 - Prob. 38CCCh. 24.7 - Prob. 5LTSCh. 24.7 - Prob. 39PTSCh. 24.7 - Prob. 40ATSCh. 24.7 - Prob. 41CCCh. 24 - Prob. 42PPCh. 24 - Prob. 43PPCh. 24 - Prob. 44PPCh. 24 - Prob. 45PPCh. 24 - Prob. 46PPCh. 24 - Prob. 47PPCh. 24 - Prob. 48PPCh. 24 - Prob. 49PPCh. 24 - Prob. 50PPCh. 24 - Prob. 51PPCh. 24 - Prob. 52PPCh. 24 - Prob. 53PPCh. 24 - Prob. 54PPCh. 24 - Prob. 55PPCh. 24 - Prob. 56PPCh. 24 - Prob. 57PPCh. 24 - Prob. 58PPCh. 24 - Prob. 59PPCh. 24 - Prob. 60PPCh. 24 - Prob. 61PPCh. 24 - Prob. 62PPCh. 24 - Prob. 63PPCh. 24 - Prob. 64PPCh. 24 - Prob. 65PPCh. 24 - Prob. 66PPCh. 24 - Prob. 67PPCh. 24 - Prob. 68PPCh. 24 - Prob. 69PPCh. 24 - Prob. 70PPCh. 24 - Prob. 71PPCh. 24 - Prob. 72PPCh. 24 - Prob. 73PPCh. 24 - Prob. 74PPCh. 24 - Prob. 75PPCh. 24 - Prob. 76PPCh. 24 - Prob. 77PPCh. 24 - Prob. 78PPCh. 24 - Prob. 79PPCh. 24 - Prob. 80PPCh. 24 - Prob. 81IPCh. 24 - Prob. 82IPCh. 24 - Prob. 83IPCh. 24 - Prob. 84IP
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