(a) Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified. Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO 3 . The oxidation of aldoses leads to the formation of aldaric acid.

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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 28, Problem 28.24P

Interpretation Introduction

(a)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Interpretation Introduction

(b)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Interpretation Introduction

(c)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

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22.7 Predict the monoalkylated products of the following reactions with benzene. (a) AlCl3 Ya (b) AlCl3 (c) H3PO4 (d) 22.8 Think-Pair-Share AICI3 The reaction below is a common electrophilic aromatic substitution. SO3 H₂SO4 SO₂H (a) Draw the reaction mechanism for this reaction using HSO,+ as the electrophile. (b) Sketch the reaction coordinate diagram, where the product is lower in energy than the starting reactant. (c) Which step in the reaction mechanism is highest in energy? Explain. (d) Which of the following reaction conditions could be used in an electrophilic aro- matic substitution with benzene to provide substituted phenyl derivatives? (i) AICI3 HNO3 H₂SO4 K2Cr2O7 (iii) H₂SO4 (iv) H₂PO₁

Is an acid-base reaction the only type of reaction that would cause leavening products to rise?

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 28, Problem 28.24P

Interpretation Introduction

(a)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Interpretation Introduction

(b)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Interpretation Introduction

(c)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Expert Solution & Answer

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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 28, Problem 28.24P

Interpretation Introduction

(a)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Interpretation Introduction

(b)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Interpretation Introduction

(c)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

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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 28, Problem 28.24P

Interpretation Introduction

(a)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Interpretation Introduction

(b)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Interpretation Introduction

(c)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

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Answer 5

Chapter 28, Problem 28.24P

Interpretation Introduction

(a)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Interpretation Introduction

(b)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Interpretation Introduction

(c)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Answer 6

Chapter 28, Problem 28.24P

Interpretation Introduction

(a)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Answer 7

Chapter 28, Problem 28.24P

Interpretation Introduction

(a)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Answer 8

Interpretation Introduction

(b)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Answer 9

Interpretation Introduction

(b)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Answer 10

Interpretation Introduction

(c)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Answer 11

Interpretation Introduction

(c)

Interpretation: The given aldose is oxidized to optically inactive aldaric acid or not is to be identified.

Concept introduction: The aldehyde group and primary alcohol of aldoses oxidizes to carboxyl groups on treatment with warm HNO3. The oxidation of aldoses leads to the formation of aldaric acid.

Answer 12

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Answer 13

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Answer 14

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Answer 15

Ch. 28 - Prob. 28.1P Ch. 28 - Prob. 28.2P Ch. 28 - Label each stereogenic center as R or S. a. b. c....Ch. 28 - Convert the ball-and-stick model to a Fischer...Ch. 28 - Prob. 28.5P Ch. 28 - Prob. 28.6P Ch. 28 - Prob. 28.7P Ch. 28 - Prob. 28.8P Ch. 28 - Prob. 28.9P Ch. 28 - Prob. 28.10P

Solution Summary: The author explains that D-erythrose is oxidized to optically inactive aldaric acid.

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Chapter 28 Solutions