We have to explain why the acid-catalyzed hydration of alkenes generally gives a secondary or a tertiary alcohol, with the exception of ethylene (H 2 C=CH 2 ) which upon acid catalyzed hydration gives a primary alcohol, ethanol. Concept introduction: The acid catalyzed hydration of an alkene involves the addition of proton to the double bonded carbon atom resulting in the formation of carbocation, bond formation between carbocation and the nucleophile, H 2 O and the deprotonation to give alcohol.

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Answer 1

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Chapter 13, Problem 67P

Interpretation Introduction

Interpretation:

We have to explain why the acid-catalyzed hydration of alkenes generally gives a secondary or a tertiary alcohol, with the exception of ethylene (H₂ C=CH₂ ) which upon acid catalyzed hydration gives a primary alcohol, ethanol.

Concept introduction:

The acid catalyzed hydration of an alkene involves the addition of proton to the double bonded carbon atom resulting in the formation of carbocation, bond formation between carbocation and the nucleophile, H₂ O and the deprotonation to give alcohol.

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Answer 2

Question

Chapter 13, Problem 67P

Interpretation Introduction

Interpretation:

We have to explain why the acid-catalyzed hydration of alkenes generally gives a secondary or a tertiary alcohol, with the exception of ethylene (H₂ C=CH₂ ) which upon acid catalyzed hydration gives a primary alcohol, ethanol.

Concept introduction:

The acid catalyzed hydration of an alkene involves the addition of proton to the double bonded carbon atom resulting in the formation of carbocation, bond formation between carbocation and the nucleophile, H₂ O and the deprotonation to give alcohol.

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Answer 3

Question

Chapter 13, Problem 67P

Interpretation Introduction

Interpretation:

We have to explain why the acid-catalyzed hydration of alkenes generally gives a secondary or a tertiary alcohol, with the exception of ethylene (H₂ C=CH₂ ) which upon acid catalyzed hydration gives a primary alcohol, ethanol.

Concept introduction:

The acid catalyzed hydration of an alkene involves the addition of proton to the double bonded carbon atom resulting in the formation of carbocation, bond formation between carbocation and the nucleophile, H₂ O and the deprotonation to give alcohol.

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Answer 4

Question

Chapter 13, Problem 67P

Interpretation Introduction

Interpretation:

We have to explain why the acid-catalyzed hydration of alkenes generally gives a secondary or a tertiary alcohol, with the exception of ethylene (H₂ C=CH₂ ) which upon acid catalyzed hydration gives a primary alcohol, ethanol.

Concept introduction:

The acid catalyzed hydration of an alkene involves the addition of proton to the double bonded carbon atom resulting in the formation of carbocation, bond formation between carbocation and the nucleophile, H₂ O and the deprotonation to give alcohol.

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Answer 5

Chapter 13, Problem 67P

Interpretation Introduction

Interpretation:

We have to explain why the acid-catalyzed hydration of alkenes generally gives a secondary or a tertiary alcohol, with the exception of ethylene (H₂ C=CH₂ ) which upon acid catalyzed hydration gives a primary alcohol, ethanol.

Concept introduction:

The acid catalyzed hydration of an alkene involves the addition of proton to the double bonded carbon atom resulting in the formation of carbocation, bond formation between carbocation and the nucleophile, H₂ O and the deprotonation to give alcohol.

Answer 6

Chapter 13, Problem 67P

Interpretation Introduction

Interpretation:

We have to explain why the acid-catalyzed hydration of alkenes generally gives a secondary or a tertiary alcohol, with the exception of ethylene (H₂ C=CH₂ ) which upon acid catalyzed hydration gives a primary alcohol, ethanol.

Concept introduction:

The acid catalyzed hydration of an alkene involves the addition of proton to the double bonded carbon atom resulting in the formation of carbocation, bond formation between carbocation and the nucleophile, H₂ O and the deprotonation to give alcohol.

Answer 7

Chapter 13, Problem 67P

Interpretation Introduction

Interpretation:

We have to explain why the acid-catalyzed hydration of alkenes generally gives a secondary or a tertiary alcohol, with the exception of ethylene (H₂ C=CH₂ ) which upon acid catalyzed hydration gives a primary alcohol, ethanol.

Concept introduction:

The acid catalyzed hydration of an alkene involves the addition of proton to the double bonded carbon atom resulting in the formation of carbocation, bond formation between carbocation and the nucleophile, H₂ O and the deprotonation to give alcohol.

Answer 8

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Answer 9

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Answer 11

Ch. 13.1 - Prob. 13.1QC Ch. 13.1 - Prob. 13.2QC Ch. 13.2 - Problem 14-3 Draw structural formulas for the...Ch. 13.2 - Prob. 13.4QC Ch. 13.2 - Prob. 13.5QC Ch. 13.3 - Problem 14-6 Write the common name for each ether.Ch. 13.4 - Prob. 13.7QC Ch. 13.4 - Prob. 13.8QC Ch. 13 - 14-8 Answer true or false. The functional group of...Ch. 13 - 14-9 What is the difference in structure between a...

Solution Summary: The author explains that acid-catalyzed hydration of alkenes generally gives a secondary or tertiary alcohol, with the exception of ethylene.

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