The trends in the increasing acidity of phenol and monofluoro derivatives of phenol have to be explained. Concept Introduction: Acidity of phenol with fluoro substitution: Halogens show inductive effect. Among the halogens, the most electronegative fluorine atom show effective inductive effect on its attachment with phenol due to which the acidity of phenol increases. If the fluorine atom is at closer position to the hydroxide group of phenol, then the inductive will be stronger due to the smaller distance which ultimately increases the acidity.

Question

The reaction Q(g) + R(g) → Z(l) is shown to be exothermic. Which of the following is true concerning the reaction

Answer 1

Question

Chapter 21, Problem 21.36P

Interpretation Introduction

Interpretation: The trends in the increasing acidity of phenol and monofluoro derivatives of phenol have to be explained.

Concept Introduction:

Acidity of phenol with fluoro substitution:

Halogens show inductive effect. Among the halogens, the most electronegative fluorine atom show effective inductive effect on its attachment with phenol due to which the acidity of phenol increases. If the fluorine atom is at closer position to the hydroxide group of phenol, then the inductive will be stronger due to the smaller distance which ultimately increases the acidity.

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Answer 2

Question

Chapter 21, Problem 21.36P

Interpretation Introduction

Interpretation: The trends in the increasing acidity of phenol and monofluoro derivatives of phenol have to be explained.

Concept Introduction:

Acidity of phenol with fluoro substitution:

Halogens show inductive effect. Among the halogens, the most electronegative fluorine atom show effective inductive effect on its attachment with phenol due to which the acidity of phenol increases. If the fluorine atom is at closer position to the hydroxide group of phenol, then the inductive will be stronger due to the smaller distance which ultimately increases the acidity.

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Answer 3

Question

Chapter 21, Problem 21.36P

Interpretation Introduction

Interpretation: The trends in the increasing acidity of phenol and monofluoro derivatives of phenol have to be explained.

Concept Introduction:

Acidity of phenol with fluoro substitution:

Halogens show inductive effect. Among the halogens, the most electronegative fluorine atom show effective inductive effect on its attachment with phenol due to which the acidity of phenol increases. If the fluorine atom is at closer position to the hydroxide group of phenol, then the inductive will be stronger due to the smaller distance which ultimately increases the acidity.

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Answer 4

Question

Chapter 21, Problem 21.36P

Interpretation Introduction

Interpretation: The trends in the increasing acidity of phenol and monofluoro derivatives of phenol have to be explained.

Concept Introduction:

Acidity of phenol with fluoro substitution:

Halogens show inductive effect. Among the halogens, the most electronegative fluorine atom show effective inductive effect on its attachment with phenol due to which the acidity of phenol increases. If the fluorine atom is at closer position to the hydroxide group of phenol, then the inductive will be stronger due to the smaller distance which ultimately increases the acidity.

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Answer 5

Chapter 21, Problem 21.36P

Interpretation Introduction

Interpretation: The trends in the increasing acidity of phenol and monofluoro derivatives of phenol have to be explained.

Concept Introduction:

Acidity of phenol with fluoro substitution:

Halogens show inductive effect. Among the halogens, the most electronegative fluorine atom show effective inductive effect on its attachment with phenol due to which the acidity of phenol increases. If the fluorine atom is at closer position to the hydroxide group of phenol, then the inductive will be stronger due to the smaller distance which ultimately increases the acidity.

Answer 6

Chapter 21, Problem 21.36P

Interpretation Introduction

Interpretation: The trends in the increasing acidity of phenol and monofluoro derivatives of phenol have to be explained.

Concept Introduction:

Acidity of phenol with fluoro substitution:

Halogens show inductive effect. Among the halogens, the most electronegative fluorine atom show effective inductive effect on its attachment with phenol due to which the acidity of phenol increases. If the fluorine atom is at closer position to the hydroxide group of phenol, then the inductive will be stronger due to the smaller distance which ultimately increases the acidity.

Answer 7

Chapter 21, Problem 21.36P

Interpretation Introduction

Interpretation: The trends in the increasing acidity of phenol and monofluoro derivatives of phenol have to be explained.

Concept Introduction:

Acidity of phenol with fluoro substitution:

Halogens show inductive effect. Among the halogens, the most electronegative fluorine atom show effective inductive effect on its attachment with phenol due to which the acidity of phenol increases. If the fluorine atom is at closer position to the hydroxide group of phenol, then the inductive will be stronger due to the smaller distance which ultimately increases the acidity.

Answer 8

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Answer 19

Ch. 21.2 - Construct a Frost circle for a planar...Ch. 21.2 - Which compound gives a signal in the 1H-NMR...Ch. 21.2 - Prob. 21.3P Ch. 21.2 - Prob. 21.4P Ch. 21.3 - Prob. 21.5P Ch. 21.4 - Arrange these compounds in order of increasing...Ch. 21.4 - Prob. AQ Ch. 21.4 - Prob. BQ Ch. 21.4 - Prob. CQ Ch. 21.5 - Prob. 21.7P

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Chapter 21 Solutions