Among the two molecules CH 3 CN and CH 3 NC , the stronger acid is to be determined, with explanation. Concept introduction: The acidity of a compound is governed largely by the functional group on which the acidic proton is found. The acid with the lower pKa value is the stronger acid. While comparing two uncharged acids, the stronger acid is the one whose negatively charged conjugate base is more stable. Delocalization of the charge via resonance lowers the concentration of the charge and increases the stability of the charged species.

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Answer 1

Question

Chapter 6, Problem 6.81P

Interpretation Introduction

Interpretation:

Among the two molecules CH3CN and CH3NC, the stronger acid is to be determined, with explanation.

Concept introduction:

The acidity of a compound is governed largely by the functional group on which the acidic proton is found. The acid with the lower pKa value is the stronger acid. While comparing two uncharged acids, the stronger acid is the one whose negatively charged conjugate base is more stable. Delocalization of the charge via resonance lowers the concentration of the charge and increases the stability of the charged species.

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4. Draw and label all possible isomers for [M(py)3(DMSO)2(CI)] (py = pyridine, DMSO dimethylsulfoxide).

Answer 2

Question

Chapter 6, Problem 6.81P

Interpretation Introduction

Interpretation:

Among the two molecules CH3CN and CH3NC, the stronger acid is to be determined, with explanation.

Concept introduction:

The acidity of a compound is governed largely by the functional group on which the acidic proton is found. The acid with the lower pKa value is the stronger acid. While comparing two uncharged acids, the stronger acid is the one whose negatively charged conjugate base is more stable. Delocalization of the charge via resonance lowers the concentration of the charge and increases the stability of the charged species.

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Answer 3

Question

Chapter 6, Problem 6.81P

Interpretation Introduction

Interpretation:

Among the two molecules CH3CN and CH3NC, the stronger acid is to be determined, with explanation.

Concept introduction:

The acidity of a compound is governed largely by the functional group on which the acidic proton is found. The acid with the lower pKa value is the stronger acid. While comparing two uncharged acids, the stronger acid is the one whose negatively charged conjugate base is more stable. Delocalization of the charge via resonance lowers the concentration of the charge and increases the stability of the charged species.

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Answer 4

Question

Chapter 6, Problem 6.81P

Interpretation Introduction

Interpretation:

Among the two molecules CH3CN and CH3NC, the stronger acid is to be determined, with explanation.

Concept introduction:

The acidity of a compound is governed largely by the functional group on which the acidic proton is found. The acid with the lower pKa value is the stronger acid. While comparing two uncharged acids, the stronger acid is the one whose negatively charged conjugate base is more stable. Delocalization of the charge via resonance lowers the concentration of the charge and increases the stability of the charged species.

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Answer 5

Chapter 6, Problem 6.81P

Interpretation Introduction

Interpretation:

Among the two molecules CH3CN and CH3NC, the stronger acid is to be determined, with explanation.

Concept introduction:

The acidity of a compound is governed largely by the functional group on which the acidic proton is found. The acid with the lower pKa value is the stronger acid. While comparing two uncharged acids, the stronger acid is the one whose negatively charged conjugate base is more stable. Delocalization of the charge via resonance lowers the concentration of the charge and increases the stability of the charged species.

Answer 6

Chapter 6, Problem 6.81P

Interpretation Introduction

Interpretation:

Among the two molecules CH3CN and CH3NC, the stronger acid is to be determined, with explanation.

Concept introduction:

The acidity of a compound is governed largely by the functional group on which the acidic proton is found. The acid with the lower pKa value is the stronger acid. While comparing two uncharged acids, the stronger acid is the one whose negatively charged conjugate base is more stable. Delocalization of the charge via resonance lowers the concentration of the charge and increases the stability of the charged species.

Answer 7

Chapter 6, Problem 6.81P

Interpretation Introduction

Interpretation:

Among the two molecules CH3CN and CH3NC, the stronger acid is to be determined, with explanation.

Concept introduction:

The acidity of a compound is governed largely by the functional group on which the acidic proton is found. The acid with the lower pKa value is the stronger acid. While comparing two uncharged acids, the stronger acid is the one whose negatively charged conjugate base is more stable. Delocalization of the charge via resonance lowers the concentration of the charge and increases the stability of the charged species.

Answer 8

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Answer 11

Ch. 6 - Prob. 6.1P Ch. 6 - Prob. 6.2P Ch. 6 - Prob. 6.3P Ch. 6 - Prob. 6.4P Ch. 6 - Prob. 6.5P Ch. 6 - Prob. 6.6P Ch. 6 - Prob. 6.7P Ch. 6 - Prob. 6.8P Ch. 6 - Prob. 6.9P Ch. 6 - Prob. 6.10P

Solution Summary: The author explains that the stronger acid is governed by the functional group on which the acidic proton is found.

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