An explanation has to be given why the enol form of phenol is more stable than its keto form. Concept Introduction: Keto-Enol Tautomers: Aldehydes and ketones many exist is an equilibrium mixture of two constitutional or structural isomers called tautomers. Tautomers differ from one another in placement of a hydrogen atom and a double bond. One tautomer is the keto form. The keto form has the structural typical of an aldehyde or ketone. The other form is called the enol form. The enol form has a structure containing a carbon-carbon double bond (en) and a hydroxyl group, the functional group of alcohols (ol). The keto form of aldehydes and ketones is most stable.

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Answer 1

Question

Chapter 13, Problem 12MCP

Interpretation Introduction

Interpretation:

An explanation has to be given why the enol form of phenol is more stable than its keto form.

Concept Introduction:

Keto-Enol Tautomers:

Aldehydes and ketones many exist is an equilibrium mixture of two constitutional or structural isomers called tautomers. Tautomers differ from one another in placement of a hydrogen atom and a double bond. One tautomer is the keto form. The keto form has the structural typical of an aldehyde or ketone. The other form is called the enol form.

The enol form has a structure containing a carbon-carbon double bond (en) and a hydroxyl group, the functional group of alcohols (ol). The keto form of aldehydes and ketones is most stable.

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Answer 2

Question

Chapter 13, Problem 12MCP

Interpretation Introduction

Interpretation:

An explanation has to be given why the enol form of phenol is more stable than its keto form.

Concept Introduction:

Keto-Enol Tautomers:

Aldehydes and ketones many exist is an equilibrium mixture of two constitutional or structural isomers called tautomers. Tautomers differ from one another in placement of a hydrogen atom and a double bond. One tautomer is the keto form. The keto form has the structural typical of an aldehyde or ketone. The other form is called the enol form.

The enol form has a structure containing a carbon-carbon double bond (en) and a hydroxyl group, the functional group of alcohols (ol). The keto form of aldehydes and ketones is most stable.

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Answer 3

Question

Chapter 13, Problem 12MCP

Interpretation Introduction

Interpretation:

An explanation has to be given why the enol form of phenol is more stable than its keto form.

Concept Introduction:

Keto-Enol Tautomers:

Aldehydes and ketones many exist is an equilibrium mixture of two constitutional or structural isomers called tautomers. Tautomers differ from one another in placement of a hydrogen atom and a double bond. One tautomer is the keto form. The keto form has the structural typical of an aldehyde or ketone. The other form is called the enol form.

The enol form has a structure containing a carbon-carbon double bond (en) and a hydroxyl group, the functional group of alcohols (ol). The keto form of aldehydes and ketones is most stable.

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Answer 4

Question

Chapter 13, Problem 12MCP

Interpretation Introduction

Interpretation:

An explanation has to be given why the enol form of phenol is more stable than its keto form.

Concept Introduction:

Keto-Enol Tautomers:

Aldehydes and ketones many exist is an equilibrium mixture of two constitutional or structural isomers called tautomers. Tautomers differ from one another in placement of a hydrogen atom and a double bond. One tautomer is the keto form. The keto form has the structural typical of an aldehyde or ketone. The other form is called the enol form.

The enol form has a structure containing a carbon-carbon double bond (en) and a hydroxyl group, the functional group of alcohols (ol). The keto form of aldehydes and ketones is most stable.

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Answer 5

Chapter 13, Problem 12MCP

Interpretation Introduction

Interpretation:

An explanation has to be given why the enol form of phenol is more stable than its keto form.

Concept Introduction:

Keto-Enol Tautomers:

Aldehydes and ketones many exist is an equilibrium mixture of two constitutional or structural isomers called tautomers. Tautomers differ from one another in placement of a hydrogen atom and a double bond. One tautomer is the keto form. The keto form has the structural typical of an aldehyde or ketone. The other form is called the enol form.

The enol form has a structure containing a carbon-carbon double bond (en) and a hydroxyl group, the functional group of alcohols (ol). The keto form of aldehydes and ketones is most stable.

Answer 6

Chapter 13, Problem 12MCP

Interpretation Introduction

Interpretation:

An explanation has to be given why the enol form of phenol is more stable than its keto form.

Concept Introduction:

Keto-Enol Tautomers:

Aldehydes and ketones many exist is an equilibrium mixture of two constitutional or structural isomers called tautomers. Tautomers differ from one another in placement of a hydrogen atom and a double bond. One tautomer is the keto form. The keto form has the structural typical of an aldehyde or ketone. The other form is called the enol form.

The enol form has a structure containing a carbon-carbon double bond (en) and a hydroxyl group, the functional group of alcohols (ol). The keto form of aldehydes and ketones is most stable.

Answer 7

Chapter 13, Problem 12MCP

Interpretation Introduction

Interpretation:

An explanation has to be given why the enol form of phenol is more stable than its keto form.

Concept Introduction:

Keto-Enol Tautomers:

Aldehydes and ketones many exist is an equilibrium mixture of two constitutional or structural isomers called tautomers. Tautomers differ from one another in placement of a hydrogen atom and a double bond. One tautomer is the keto form. The keto form has the structural typical of an aldehyde or ketone. The other form is called the enol form.

The enol form has a structure containing a carbon-carbon double bond (en) and a hydroxyl group, the functional group of alcohols (ol). The keto form of aldehydes and ketones is most stable.

Answer 8

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Answer 10

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Answer 11

Ch. 13.1 - Which member in each of the following pairs will...Ch. 13.1 - Which member in each of the following pairs will...Ch. 13.1 - Prob. 13.3Q Ch. 13.1 - Prob. 13.4Q Ch. 13.2 - Prob. 13.1PP Ch. 13.2 - Prob. 13.2PP Ch. 13.2 - Prob. 13.3PP Ch. 13.2 - Prob. 13.4PP Ch. 13.2 - Prob. 13.5Q Ch. 13.2 - Write the condensed formula for each of the...

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