The two enol tautomer of the given compound has to be drawn and more stable structure has to be identified. Concept Introduction: Keto-Enol tautomerization: The enol and keto are said to be tautomer, are constitutional isomers that rapidly interconvert via the migration of a proton. The interconversion between an enol and a ketone is called keto-enol tautomerization. Tautomerization is an equilibrium process, that the equilibrium will establish specific concentrations for both the enol and the ketone. Once the equilibrium is reached, the concentrations of ketone and enol can be measured. The tautomerization is catalyzed by even trace amounts of acid (or base). Tautomerism is the ability of a molecule to exist in more than one chemical form. Tautomers are formed by the migration of a hydrogen atom, accompanied by the switching of a single and neighboring double bond. The only difference in keto-enol tautomers is the location of hydrogen and double bond. Enol tautomer is much less stable than the keto tautomer. Enol tautomer is more stable when enol tautomer is aromatic or when the double bonds are conjugated. Resonance: The delocalization of electrons which is characterized as several structural changes.

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Answer 1

Question

Chapter 13.2, Problem 7P

Interpretation Introduction

Interpretation:

The two enol tautomer of the given compound has to be drawn and more stable structure has to be identified.

Concept Introduction:

Keto-Enol tautomerization: The enol and keto are said to be tautomer, are constitutional isomers that rapidly interconvert via the migration of a proton. The interconversion between an enol and a ketone is called keto-enol tautomerization. Tautomerization is an equilibrium process, that the equilibrium will establish specific concentrations for both the enol and the ketone. Once the equilibrium is reached, the concentrations of ketone and enol can be measured.

The tautomerization is catalyzed by even trace amounts of acid (or base).

Tautomerism is the ability of a molecule to exist in more than one chemical form.

Tautomers are formed by the migration of a hydrogen atom, accompanied by the switching of a single and neighboring double bond.

The only difference in keto-enol tautomers is the location of hydrogen and double bond.

Enol tautomer is much less stable than the keto tautomer.

Enol tautomer is more stable when enol tautomer is aromatic or when the double bonds are conjugated.

Resonance: The delocalization of electrons which is characterized as several structural changes.

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Answer 2

Question

Chapter 13.2, Problem 7P

Interpretation Introduction

Interpretation:

The two enol tautomer of the given compound has to be drawn and more stable structure has to be identified.

Concept Introduction:

Keto-Enol tautomerization: The enol and keto are said to be tautomer, are constitutional isomers that rapidly interconvert via the migration of a proton. The interconversion between an enol and a ketone is called keto-enol tautomerization. Tautomerization is an equilibrium process, that the equilibrium will establish specific concentrations for both the enol and the ketone. Once the equilibrium is reached, the concentrations of ketone and enol can be measured.

The tautomerization is catalyzed by even trace amounts of acid (or base).

Tautomerism is the ability of a molecule to exist in more than one chemical form.

Tautomers are formed by the migration of a hydrogen atom, accompanied by the switching of a single and neighboring double bond.

The only difference in keto-enol tautomers is the location of hydrogen and double bond.

Enol tautomer is much less stable than the keto tautomer.

Enol tautomer is more stable when enol tautomer is aromatic or when the double bonds are conjugated.

Resonance: The delocalization of electrons which is characterized as several structural changes.

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Answer 3

Question

Chapter 13.2, Problem 7P

Interpretation Introduction

Interpretation:

The two enol tautomer of the given compound has to be drawn and more stable structure has to be identified.

Concept Introduction:

Keto-Enol tautomerization: The enol and keto are said to be tautomer, are constitutional isomers that rapidly interconvert via the migration of a proton. The interconversion between an enol and a ketone is called keto-enol tautomerization. Tautomerization is an equilibrium process, that the equilibrium will establish specific concentrations for both the enol and the ketone. Once the equilibrium is reached, the concentrations of ketone and enol can be measured.

The tautomerization is catalyzed by even trace amounts of acid (or base).

Tautomerism is the ability of a molecule to exist in more than one chemical form.

Tautomers are formed by the migration of a hydrogen atom, accompanied by the switching of a single and neighboring double bond.

The only difference in keto-enol tautomers is the location of hydrogen and double bond.

Enol tautomer is much less stable than the keto tautomer.

Enol tautomer is more stable when enol tautomer is aromatic or when the double bonds are conjugated.

Resonance: The delocalization of electrons which is characterized as several structural changes.

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Answer 4

Question

Chapter 13.2, Problem 7P

Interpretation Introduction

Interpretation:

The two enol tautomer of the given compound has to be drawn and more stable structure has to be identified.

Concept Introduction:

Keto-Enol tautomerization: The enol and keto are said to be tautomer, are constitutional isomers that rapidly interconvert via the migration of a proton. The interconversion between an enol and a ketone is called keto-enol tautomerization. Tautomerization is an equilibrium process, that the equilibrium will establish specific concentrations for both the enol and the ketone. Once the equilibrium is reached, the concentrations of ketone and enol can be measured.

The tautomerization is catalyzed by even trace amounts of acid (or base).

Tautomerism is the ability of a molecule to exist in more than one chemical form.

Tautomers are formed by the migration of a hydrogen atom, accompanied by the switching of a single and neighboring double bond.

The only difference in keto-enol tautomers is the location of hydrogen and double bond.

Enol tautomer is much less stable than the keto tautomer.

Enol tautomer is more stable when enol tautomer is aromatic or when the double bonds are conjugated.

Resonance: The delocalization of electrons which is characterized as several structural changes.

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Answer 5

Chapter 13.2, Problem 7P

Interpretation Introduction

Interpretation:

The two enol tautomer of the given compound has to be drawn and more stable structure has to be identified.

Concept Introduction:

Keto-Enol tautomerization: The enol and keto are said to be tautomer, are constitutional isomers that rapidly interconvert via the migration of a proton. The interconversion between an enol and a ketone is called keto-enol tautomerization. Tautomerization is an equilibrium process, that the equilibrium will establish specific concentrations for both the enol and the ketone. Once the equilibrium is reached, the concentrations of ketone and enol can be measured.

The tautomerization is catalyzed by even trace amounts of acid (or base).

Tautomerism is the ability of a molecule to exist in more than one chemical form.

Tautomers are formed by the migration of a hydrogen atom, accompanied by the switching of a single and neighboring double bond.

The only difference in keto-enol tautomers is the location of hydrogen and double bond.

Enol tautomer is much less stable than the keto tautomer.

Enol tautomer is more stable when enol tautomer is aromatic or when the double bonds are conjugated.

Resonance: The delocalization of electrons which is characterized as several structural changes.

Answer 6

Chapter 13.2, Problem 7P

Interpretation Introduction

Interpretation:

The two enol tautomer of the given compound has to be drawn and more stable structure has to be identified.

Concept Introduction:

Keto-Enol tautomerization: The enol and keto are said to be tautomer, are constitutional isomers that rapidly interconvert via the migration of a proton. The interconversion between an enol and a ketone is called keto-enol tautomerization. Tautomerization is an equilibrium process, that the equilibrium will establish specific concentrations for both the enol and the ketone. Once the equilibrium is reached, the concentrations of ketone and enol can be measured.

The tautomerization is catalyzed by even trace amounts of acid (or base).

Tautomerism is the ability of a molecule to exist in more than one chemical form.

Tautomers are formed by the migration of a hydrogen atom, accompanied by the switching of a single and neighboring double bond.

The only difference in keto-enol tautomers is the location of hydrogen and double bond.

Enol tautomer is much less stable than the keto tautomer.

Enol tautomer is more stable when enol tautomer is aromatic or when the double bonds are conjugated.

Resonance: The delocalization of electrons which is characterized as several structural changes.

Answer 7

Chapter 13.2, Problem 7P

Interpretation Introduction

Interpretation:

The two enol tautomer of the given compound has to be drawn and more stable structure has to be identified.

Concept Introduction:

Keto-Enol tautomerization: The enol and keto are said to be tautomer, are constitutional isomers that rapidly interconvert via the migration of a proton. The interconversion between an enol and a ketone is called keto-enol tautomerization. Tautomerization is an equilibrium process, that the equilibrium will establish specific concentrations for both the enol and the ketone. Once the equilibrium is reached, the concentrations of ketone and enol can be measured.

The tautomerization is catalyzed by even trace amounts of acid (or base).

Tautomerism is the ability of a molecule to exist in more than one chemical form.

Tautomers are formed by the migration of a hydrogen atom, accompanied by the switching of a single and neighboring double bond.

The only difference in keto-enol tautomers is the location of hydrogen and double bond.

Enol tautomer is much less stable than the keto tautomer.

Enol tautomer is more stable when enol tautomer is aromatic or when the double bonds are conjugated.

Resonance: The delocalization of electrons which is characterized as several structural changes.

Answer 8

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Answer 9

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Answer 11

Ch. 13.1 - Identify the most acidic hydrogen in each...Ch. 13.1 - Prob. 2P Ch. 13.1 - Prob. 3P Ch. 13.1 - Prob. 4P Ch. 13.1 - Explain why HO cannot remove a proton from the...Ch. 13.2 - Prob. 6P Ch. 13.2 - Prob. 7P Ch. 13.3 - Prob. 8P Ch. 13.3 - Prob. 9P Ch. 13.3 - Prob. 10P

Solution Summary: The author explains that enol and keto are constitutional isomers that rapidly interconvert via the migration of a proton.

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