Reducing sugar property of salicin should be identified. Concept introduction: Reducing sugar: Sugars that contain aldehyde or a free ketone groups that are oxidized to carboxylic acids are classified as reducing sugars.

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Answer 1

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 24, Problem 76PP

(a)

Interpretation Introduction

Interpretation:

Reducing sugar property of salicin should be identified.

Concept introduction:

Reducing sugar: Sugars that contain aldehyde or a free ketone groups that are oxidized to carboxylic acids are classified as reducing sugars.

(b)

Interpretation Introduction

Interpretation:

Products should be identified when salicin is hydrolyzed in the presence of an acid

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

(c)

Interpretation Introduction

Interpretation:

Structure ofsalicin (α-glycoside or β-glycoside) should be identified.

Concept introduction:

The Haworth projection: A Haworth projection is a three-dimensional representation of monosaccharides and the structural formula is inscription as a cyclic structures.

In Haworth projection, oxygen atom is placed in back right corner, CH2OH is arranged up at the C5 carbon atom. Anomeric hydroxyl group is placed down if it is α-anomer which is trans to the CH2OH of C5 carbon. Anomeric hydroxyl group is placed up if it is β-anomer which is cis to the CH2OH of C5 carbon. The remaining hydroxyl group is placed up if the hydroxyl group left side in Fischer projection. Hydroxyl group is placed down if the hydroxyl group right side in Fischer projection

(d)

Interpretation Introduction

Interpretation:

Major product should be identified when salicin is reaction with excess acetic anhydride in the pyridine.

Concept introduction:

Acetylation: carbohydratesacetylatedby using acetic anhydride in pyridine.

(e)

Interpretation Introduction

Interpretation:

Mutarotation property of salicin should be identified when dissolved in neutral water.

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

Mutarotation: Change in the optical rotation because change inequilibrium between the α-anomer and β-anomer when the stereocenters interconvert.

The optical rotation of the solution mainly depends on the optical rotation of the α-anomer and β-anomer and ratio in the solution.

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Answer 2

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 24, Problem 76PP

(a)

Interpretation Introduction

Interpretation:

Reducing sugar property of salicin should be identified.

Concept introduction:

Reducing sugar: Sugars that contain aldehyde or a free ketone groups that are oxidized to carboxylic acids are classified as reducing sugars.

(b)

Interpretation Introduction

Interpretation:

Products should be identified when salicin is hydrolyzed in the presence of an acid

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

(c)

Interpretation Introduction

Interpretation:

Structure ofsalicin (α-glycoside or β-glycoside) should be identified.

Concept introduction:

The Haworth projection: A Haworth projection is a three-dimensional representation of monosaccharides and the structural formula is inscription as a cyclic structures.

In Haworth projection, oxygen atom is placed in back right corner, CH2OH is arranged up at the C5 carbon atom. Anomeric hydroxyl group is placed down if it is α-anomer which is trans to the CH2OH of C5 carbon. Anomeric hydroxyl group is placed up if it is β-anomer which is cis to the CH2OH of C5 carbon. The remaining hydroxyl group is placed up if the hydroxyl group left side in Fischer projection. Hydroxyl group is placed down if the hydroxyl group right side in Fischer projection

(d)

Interpretation Introduction

Interpretation:

Major product should be identified when salicin is reaction with excess acetic anhydride in the pyridine.

Concept introduction:

Acetylation: carbohydratesacetylatedby using acetic anhydride in pyridine.

(e)

Interpretation Introduction

Interpretation:

Mutarotation property of salicin should be identified when dissolved in neutral water.

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

Mutarotation: Change in the optical rotation because change inequilibrium between the α-anomer and β-anomer when the stereocenters interconvert.

The optical rotation of the solution mainly depends on the optical rotation of the α-anomer and β-anomer and ratio in the solution.

Expert Solution & Answer

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Check out a sample textbook solution

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Answer 3

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 24, Problem 76PP

(a)

Interpretation Introduction

Interpretation:

Reducing sugar property of salicin should be identified.

Concept introduction:

Reducing sugar: Sugars that contain aldehyde or a free ketone groups that are oxidized to carboxylic acids are classified as reducing sugars.

(b)

Interpretation Introduction

Interpretation:

Products should be identified when salicin is hydrolyzed in the presence of an acid

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

(c)

Interpretation Introduction

Interpretation:

Structure ofsalicin (α-glycoside or β-glycoside) should be identified.

Concept introduction:

The Haworth projection: A Haworth projection is a three-dimensional representation of monosaccharides and the structural formula is inscription as a cyclic structures.

In Haworth projection, oxygen atom is placed in back right corner, CH2OH is arranged up at the C5 carbon atom. Anomeric hydroxyl group is placed down if it is α-anomer which is trans to the CH2OH of C5 carbon. Anomeric hydroxyl group is placed up if it is β-anomer which is cis to the CH2OH of C5 carbon. The remaining hydroxyl group is placed up if the hydroxyl group left side in Fischer projection. Hydroxyl group is placed down if the hydroxyl group right side in Fischer projection

(d)

Interpretation Introduction

Interpretation:

Major product should be identified when salicin is reaction with excess acetic anhydride in the pyridine.

Concept introduction:

Acetylation: carbohydratesacetylatedby using acetic anhydride in pyridine.

(e)

Interpretation Introduction

Interpretation:

Mutarotation property of salicin should be identified when dissolved in neutral water.

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

Mutarotation: Change in the optical rotation because change inequilibrium between the α-anomer and β-anomer when the stereocenters interconvert.

The optical rotation of the solution mainly depends on the optical rotation of the α-anomer and β-anomer and ratio in the solution.

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Answer 4

Question

Definition Definition Class of organic compounds that contain a carboxyl group ( - COOH ) and has a general formula R - COOH or R - CO 2 H , where R refers to the alkyl, alkenyl, aryl, or other groups. They can undergo different chemical reactions, such as acid-base reactions, esterification, and oxidation. These are essential components of living organisms, playing important roles in metabolic processes, signaling, and as pharmaceuticals.

Chapter 24, Problem 76PP

(a)

Interpretation Introduction

Interpretation:

Reducing sugar property of salicin should be identified.

Concept introduction:

Reducing sugar: Sugars that contain aldehyde or a free ketone groups that are oxidized to carboxylic acids are classified as reducing sugars.

(b)

Interpretation Introduction

Interpretation:

Products should be identified when salicin is hydrolyzed in the presence of an acid

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

(c)

Interpretation Introduction

Interpretation:

Structure ofsalicin (α-glycoside or β-glycoside) should be identified.

Concept introduction:

The Haworth projection: A Haworth projection is a three-dimensional representation of monosaccharides and the structural formula is inscription as a cyclic structures.

In Haworth projection, oxygen atom is placed in back right corner, CH2OH is arranged up at the C5 carbon atom. Anomeric hydroxyl group is placed down if it is α-anomer which is trans to the CH2OH of C5 carbon. Anomeric hydroxyl group is placed up if it is β-anomer which is cis to the CH2OH of C5 carbon. The remaining hydroxyl group is placed up if the hydroxyl group left side in Fischer projection. Hydroxyl group is placed down if the hydroxyl group right side in Fischer projection

(d)

Interpretation Introduction

Interpretation:

Major product should be identified when salicin is reaction with excess acetic anhydride in the pyridine.

Concept introduction:

Acetylation: carbohydratesacetylatedby using acetic anhydride in pyridine.

(e)

Interpretation Introduction

Interpretation:

Mutarotation property of salicin should be identified when dissolved in neutral water.

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

Mutarotation: Change in the optical rotation because change inequilibrium between the α-anomer and β-anomer when the stereocenters interconvert.

The optical rotation of the solution mainly depends on the optical rotation of the α-anomer and β-anomer and ratio in the solution.

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Answer 5

Chapter 24, Problem 76PP

(a)

Interpretation Introduction

Interpretation:

Reducing sugar property of salicin should be identified.

Concept introduction:

Reducing sugar: Sugars that contain aldehyde or a free ketone groups that are oxidized to carboxylic acids are classified as reducing sugars.

(b)

Interpretation Introduction

Interpretation:

Products should be identified when salicin is hydrolyzed in the presence of an acid

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

(c)

Interpretation Introduction

Interpretation:

Structure ofsalicin (α-glycoside or β-glycoside) should be identified.

Concept introduction:

The Haworth projection: A Haworth projection is a three-dimensional representation of monosaccharides and the structural formula is inscription as a cyclic structures.

In Haworth projection, oxygen atom is placed in back right corner, CH2OH is arranged up at the C5 carbon atom. Anomeric hydroxyl group is placed down if it is α-anomer which is trans to the CH2OH of C5 carbon. Anomeric hydroxyl group is placed up if it is β-anomer which is cis to the CH2OH of C5 carbon. The remaining hydroxyl group is placed up if the hydroxyl group left side in Fischer projection. Hydroxyl group is placed down if the hydroxyl group right side in Fischer projection

(d)

Interpretation Introduction

Interpretation:

Major product should be identified when salicin is reaction with excess acetic anhydride in the pyridine.

Concept introduction:

Acetylation: carbohydratesacetylatedby using acetic anhydride in pyridine.

(e)

Interpretation Introduction

Interpretation:

Mutarotation property of salicin should be identified when dissolved in neutral water.

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

Mutarotation: Change in the optical rotation because change inequilibrium between the α-anomer and β-anomer when the stereocenters interconvert.

The optical rotation of the solution mainly depends on the optical rotation of the α-anomer and β-anomer and ratio in the solution.

Answer 6

Chapter 24, Problem 76PP

(a)

Interpretation Introduction

Interpretation:

Reducing sugar property of salicin should be identified.

Concept introduction:

Reducing sugar: Sugars that contain aldehyde or a free ketone groups that are oxidized to carboxylic acids are classified as reducing sugars.

Answer 7

Chapter 24, Problem 76PP

(a)

Interpretation Introduction

Interpretation:

Reducing sugar property of salicin should be identified.

Concept introduction:

Reducing sugar: Sugars that contain aldehyde or a free ketone groups that are oxidized to carboxylic acids are classified as reducing sugars.

Answer 8

(b)

Interpretation Introduction

Interpretation:

Products should be identified when salicin is hydrolyzed in the presence of an acid

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

Answer 9

(b)

Interpretation Introduction

Interpretation:

Products should be identified when salicin is hydrolyzed in the presence of an acid

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

Answer 10

(c)

Interpretation Introduction

Interpretation:

Structure ofsalicin (α-glycoside or β-glycoside) should be identified.

Concept introduction:

The Haworth projection: A Haworth projection is a three-dimensional representation of monosaccharides and the structural formula is inscription as a cyclic structures.

In Haworth projection, oxygen atom is placed in back right corner, CH2OH is arranged up at the C5 carbon atom. Anomeric hydroxyl group is placed down if it is α-anomer which is trans to the CH2OH of C5 carbon. Anomeric hydroxyl group is placed up if it is β-anomer which is cis to the CH2OH of C5 carbon. The remaining hydroxyl group is placed up if the hydroxyl group left side in Fischer projection. Hydroxyl group is placed down if the hydroxyl group right side in Fischer projection

Answer 11

(c)

Interpretation Introduction

Interpretation:

Structure ofsalicin (α-glycoside or β-glycoside) should be identified.

Concept introduction:

The Haworth projection: A Haworth projection is a three-dimensional representation of monosaccharides and the structural formula is inscription as a cyclic structures.

In Haworth projection, oxygen atom is placed in back right corner, CH2OH is arranged up at the C5 carbon atom. Anomeric hydroxyl group is placed down if it is α-anomer which is trans to the CH2OH of C5 carbon. Anomeric hydroxyl group is placed up if it is β-anomer which is cis to the CH2OH of C5 carbon. The remaining hydroxyl group is placed up if the hydroxyl group left side in Fischer projection. Hydroxyl group is placed down if the hydroxyl group right side in Fischer projection

Answer 12

(d)

Interpretation Introduction

Interpretation:

Major product should be identified when salicin is reaction with excess acetic anhydride in the pyridine.

Concept introduction:

Acetylation: carbohydratesacetylatedby using acetic anhydride in pyridine.

Answer 13

(d)

Interpretation Introduction

Interpretation:

Major product should be identified when salicin is reaction with excess acetic anhydride in the pyridine.

Concept introduction:

Acetylation: carbohydratesacetylatedby using acetic anhydride in pyridine.

Answer 14

(e)

Interpretation Introduction

Interpretation:

Mutarotation property of salicin should be identified when dissolved in neutral water.

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

Mutarotation: Change in the optical rotation because change inequilibrium between the α-anomer and β-anomer when the stereocenters interconvert.

The optical rotation of the solution mainly depends on the optical rotation of the α-anomer and β-anomer and ratio in the solution.

Answer 15

(e)

Interpretation Introduction

Interpretation:

Mutarotation property of salicin should be identified when dissolved in neutral water.

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

Mutarotation: Change in the optical rotation because change inequilibrium between the α-anomer and β-anomer when the stereocenters interconvert.

The optical rotation of the solution mainly depends on the optical rotation of the α-anomer and β-anomer and ratio in the solution.

Answer 16

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Answer 17

Expert Solution & Answer

Answer 18

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Answer 19

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

Reducing sugar property of salicin should be identified. Concept introduction: Reducing sugar: Sugars that contain aldehyde or a free ketone groups that are oxidized to carboxylic acids are classified as reducing sugars.

Interpretation: Reducing sugar property of salicin should be identified. Concept introduction: Reducing sugar: Sugars that contain aldehyde or a free ketone groups that are oxidized to carboxylic acids are classified as reducing sugars.

Interpretation: Products should be identified when salicin is hydrolyzed in the presence of an acid Concept introduction: Acid: acid hydrolysis the ethers which produces alcohols.

Interpretation: Major product should be identified when salicin is reaction with excess acetic anhydride in the pyridine. Concept introduction: Acetylation: carbohydratesacetylatedby using acetic anhydride in pyridine.

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Chapter 24 Solutions

Interpretation:

Reducing sugar property of salicin should be identified.

Concept introduction:

Reducing sugar: Sugars that contain aldehyde or a free ketone groups that are oxidized to carboxylic acids are classified as reducing sugars.

Interpretation:

Products should be identified when salicin is hydrolyzed in the presence of an acid

Concept introduction:

Acid: acid hydrolysis the ethers which produces alcohols.

Interpretation:

Major product should be identified when salicin is reaction with excess acetic anhydride in the pyridine.

Concept introduction:

Acetylation: carbohydratesacetylatedby using acetic anhydride in pyridine.