(a) Interpretation: All resonance structures for the radical that result from the homolysis of OH bond are to be drawn. Concept introduction: The general steps followed by free-radical reaction are stated below: 1. First step is initiation that involves formation of radical. 2. Second step is propagation. 3. Third step is the termination that involves the formation of stable bond.

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Answer 1

Question

Chapter 15, Problem 15.69P

Interpretation Introduction

(a)

Interpretation: All resonance structures for the radical that result from the homolysis of OH bond are to be drawn.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

Interpretation Introduction

(b)

Interpretation: An explanation for the given statement that the homolysis of this OH bond is preferred to the homolysis of either OH bond in the other benzene ring is to be stated.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

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JON Determine the bund energy for UCI (in kJ/mol Hcl) using me balanced chemical equation and bund energies listed? का (My (9) +36/2(g)-(((3(g) + 3(g) A Hryn = -330. KJ bond energy и-н 432 bond bond C-1413 C=C 839 N-H 391 C=O 1010 S-H 363 б-н 467 02 498 N-N 160 N=N 243 418 C-C 341 C-0 358 C=C C-C 339 N-Br 243 Br-Br C-Br 274 193 614 (-1 214||(=olin (02) 799 C=N 615 AAL

Determine the bond energy for HCI ( in kJ/mol HCI) using he balanced cremiculequecticnand bund energles listed? also c double bond to N is 615, read numbets carefully please!!!! Determine the bund energy for UCI (in kJ/mol cl) using me balanced chemical equation and bund energies listed? 51 (My (9) +312(g)-73(g) + 3(g) =-330. KJ спод bond energy Hryn H-H bond band 432 C-1 413 C=C 839 NH 391 C=O 1010 S-1 343 6-H 02 498 N-N 160 467 N=N C-C 341 CL- 243 418 339 N-Br 243 C-O 358 Br-Br C=C C-Br 274 193 614 (-1 216 (=olin (02) 799 C=N 618

Please correct answer and don't used hand raiting

Answer 2

Question

Chapter 15, Problem 15.69P

Interpretation Introduction

(a)

Interpretation: All resonance structures for the radical that result from the homolysis of OH bond are to be drawn.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

Interpretation Introduction

(b)

Interpretation: An explanation for the given statement that the homolysis of this OH bond is preferred to the homolysis of either OH bond in the other benzene ring is to be stated.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

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Answer 3

Question

Chapter 15, Problem 15.69P

Interpretation Introduction

(a)

Interpretation: All resonance structures for the radical that result from the homolysis of OH bond are to be drawn.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

Interpretation Introduction

(b)

Interpretation: An explanation for the given statement that the homolysis of this OH bond is preferred to the homolysis of either OH bond in the other benzene ring is to be stated.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

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Answer 4

Question

Chapter 15, Problem 15.69P

Interpretation Introduction

(a)

Interpretation: All resonance structures for the radical that result from the homolysis of OH bond are to be drawn.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

Interpretation Introduction

(b)

Interpretation: An explanation for the given statement that the homolysis of this OH bond is preferred to the homolysis of either OH bond in the other benzene ring is to be stated.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

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Answer 5

Chapter 15, Problem 15.69P

Interpretation Introduction

(a)

Interpretation: All resonance structures for the radical that result from the homolysis of OH bond are to be drawn.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

Interpretation Introduction

(b)

Interpretation: An explanation for the given statement that the homolysis of this OH bond is preferred to the homolysis of either OH bond in the other benzene ring is to be stated.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

Answer 6

Chapter 15, Problem 15.69P

Interpretation Introduction

(a)

Interpretation: All resonance structures for the radical that result from the homolysis of OH bond are to be drawn.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

Answer 7

Chapter 15, Problem 15.69P

Interpretation Introduction

(a)

Interpretation: All resonance structures for the radical that result from the homolysis of OH bond are to be drawn.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

Answer 8

Interpretation Introduction

(b)

Interpretation: An explanation for the given statement that the homolysis of this OH bond is preferred to the homolysis of either OH bond in the other benzene ring is to be stated.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

Answer 9

Interpretation Introduction

(b)

Interpretation: An explanation for the given statement that the homolysis of this OH bond is preferred to the homolysis of either OH bond in the other benzene ring is to be stated.

Concept introduction: The general steps followed by free-radical reaction are stated below:

1. First step is initiation that involves formation of radical.

2. Second step is propagation.

3. Third step is the termination that involves the formation of stable bond.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 15 - Prob. 15.1P Ch. 15 - Prob. 15.2P Ch. 15 - Draw the product formed when a chlorine atom (Cl)...Ch. 15 - Prob. 15.4P Ch. 15 - Prob. 15.5P Ch. 15 - Problem 15.6 Using mechanism 15.1 as guide, write...Ch. 15 - Calculate m0 for the two propagation steps in the...Ch. 15 - Prob. 15.8P Ch. 15 - Problem 15.8 Which bond in the each compound is...Ch. 15 - Prob. 15.10P

Solution Summary: The author explains that the radical formed by the homolysis of OH bond is shown in Figure 1.

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