Furanose forms of D-Erythrose and D-Threose are needed to be drawn. Concept introduction: Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom. The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring. α-indicates the –OH group of anomeric carbon C1 is directed to down side. β-indicates the –OH group of anomeric carbon C1 is directed to upward side. The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively. To draw: the Furanose form of α-D-Erythrofuranose.

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Answer 1

Question

Chapter 24.5, Problem 19CC

(a)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Erythrofuranose.

(b)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Erythrofuranose.

(c)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Threofuranose.

(d)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Threofuranose.

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What I Have Learned Directions: Given the following reaction and the stress applied in each reaction, answer the question below. A. H2(g) + Cl2(g) 2 HCl(g) Stress applied: Decreasing the pressure 1. What is the Keq expression? 2. What will be the effect in the number of moles of HCl(g)? 3. What will be the Equilibrium Shift or the reaction? B. Fe3O4(s) + 4 H2(g) + heat 53 Fe(s) + 4 H₂O(g) Stress applied: Increasing the temperature 1. What is the Keq expression?. 2. What will be the effect in the volume of water vapor collected? 3. What will be the Equilibrium Shift or the reaction? C. 4 NH3(g) + 5 O2(g) 4 NO(g) + 6 H2O(g) + heat Stress applied: Increasing the volume of the container 1. What is the Keq expression?. 2. What will be the effect in the amount of H₂O? 3. What will be the Equilibrium Shift or the reaction?

Consider the solubility products (Ksp values) for the following compounds:SrSO4 (Ksp = 7.6 x 10−7), BaSO4 (Ksp = 1.5 x 10−9), SrCO3 (Ksp = 7.0 x 10−10), BaCO3 (Ksp = 1.6 x 10−9)Which anion is the harder base, CO32− or SO42−? Justify your answer.

Answer 2

Question

Chapter 24.5, Problem 19CC

(a)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Erythrofuranose.

(b)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Erythrofuranose.

(c)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Threofuranose.

(d)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Threofuranose.

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Answer 3

Question

Chapter 24.5, Problem 19CC

(a)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Erythrofuranose.

(b)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Erythrofuranose.

(c)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Threofuranose.

(d)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Threofuranose.

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Answer 4

Question

Chapter 24.5, Problem 19CC

(a)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Erythrofuranose.

(b)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Erythrofuranose.

(c)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Threofuranose.

(d)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Threofuranose.

Expert Solution & Answer

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Check out a sample textbook solution

See solution

Answer 5

Chapter 24.5, Problem 19CC

(a)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Erythrofuranose.

(b)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Erythrofuranose.

(c)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Threofuranose.

(d)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Threofuranose.

Answer 6

Chapter 24.5, Problem 19CC

(a)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Erythrofuranose.

Answer 7

Chapter 24.5, Problem 19CC

(a)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Erythrofuranose.

Answer 8

(b)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Erythrofuranose.

Answer 9

(b)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Erythrofuranose.

Answer 10

(c)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Threofuranose.

Answer 11

(c)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of α-D-Threofuranose.

Answer 12

(d)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Threofuranose.

Answer 13

(d)

Interpretation Introduction

Interpretation:

Furanose forms of D-Erythrose and D-Threose are needed to be drawn.

Concept introduction:

Furanose is used to represent sugars in their cyclic forms. In which five-membered ring consisting of four carbon atoms and one oxygen atom.

The –OH group of C4 carbon attacks the carbonyl group of the D-aldotetroses, thereby a Furanose ring is formed by the four carbon atoms and oxygen atom of –OH group in the C4 carbon with incorporating into the ring.

α-indicates the –OH group of anomeric carbon C1 is directed to down side.

β-indicates the –OH group of anomeric carbon C1 is directed to upward side.

The right side and left side –OH groups of chiral carbons in fisher projection are drawn as down side and upward side respectively.

To draw: the Furanose form of β-D-Threofuranose.

Answer 14

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Answer 15

Expert Solution & Answer

Answer 16

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Answer 17

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

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Chapter 24 Solutions