(a) Interpretation: The synthesis of ether, ClCH 2 CH 2 OCH 2 CH 2 Cl , using either alcohol dehydration or alkene addition is to be stated. Concept introduction: The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Question

Want to see the full answer?

Answer 1

Question

Chapter 11, Problem 11.11P

Interpretation Introduction

(a)

Interpretation:

The synthesis of ether, ClCH2CH2OCH2CH2Cl, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(b)

Interpretation:

The synthesis of ether, 2−methoxy−2−methylbutane, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(c)

Interpretation:

The synthesis of ether, tert−butyl isopropyl ether, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(d)

Interpretation:

The synthesis of dibutyl ether using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms an ether.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

These are in the wrong boxes. Why does the one on the left have a lower molar mass than the one on the right?

SYNTHESIS REACTIONS. For the following reactions, synthesize the given products from the given reactants. Multiple reactions/steps will be needed. For the one of the steps (ie reactions) in each synthesis, write out the mechanism for that reaction and draw an energy diagram showing the correct number of hills and valleys for that step's mechanism. CI b. a. Use acetylene (ethyne) and any alkyl halide as your starting materials Br C. d. "OH OH III. OH

Calculate the pH and the pOH of each of the following solutions at 25 °C for which the substances ionize completely: (a) 0.200 M HCl

Answer 2

Question

Chapter 11, Problem 11.11P

Interpretation Introduction

(a)

Interpretation:

The synthesis of ether, ClCH2CH2OCH2CH2Cl, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(b)

Interpretation:

The synthesis of ether, 2−methoxy−2−methylbutane, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(c)

Interpretation:

The synthesis of ether, tert−butyl isopropyl ether, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(d)

Interpretation:

The synthesis of dibutyl ether using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms an ether.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 11, Problem 11.11P

Interpretation Introduction

(a)

Interpretation:

The synthesis of ether, ClCH2CH2OCH2CH2Cl, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(b)

Interpretation:

The synthesis of ether, 2−methoxy−2−methylbutane, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(c)

Interpretation:

The synthesis of ether, tert−butyl isopropyl ether, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(d)

Interpretation:

The synthesis of dibutyl ether using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms an ether.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 11, Problem 11.11P

Interpretation Introduction

(a)

Interpretation:

The synthesis of ether, ClCH2CH2OCH2CH2Cl, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(b)

Interpretation:

The synthesis of ether, 2−methoxy−2−methylbutane, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(c)

Interpretation:

The synthesis of ether, tert−butyl isopropyl ether, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(d)

Interpretation:

The synthesis of dibutyl ether using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms an ether.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 11, Problem 11.11P

Interpretation Introduction

(a)

Interpretation:

The synthesis of ether, ClCH2CH2OCH2CH2Cl, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(b)

Interpretation:

The synthesis of ether, 2−methoxy−2−methylbutane, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(c)

Interpretation:

The synthesis of ether, tert−butyl isopropyl ether, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Interpretation Introduction

(d)

Interpretation:

The synthesis of dibutyl ether using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms an ether.

Answer 6

Chapter 11, Problem 11.11P

Interpretation Introduction

(a)

Interpretation:

The synthesis of ether, ClCH2CH2OCH2CH2Cl, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Answer 7

Chapter 11, Problem 11.11P

Interpretation Introduction

(a)

Interpretation:

The synthesis of ether, ClCH2CH2OCH2CH2Cl, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The synthesis of ether, 2−methoxy−2−methylbutane, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The synthesis of ether, 2−methoxy−2−methylbutane, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Answer 10

Interpretation Introduction

(c)

Interpretation:

The synthesis of ether, tert−butyl isopropyl ether, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Answer 11

Interpretation Introduction

(c)

Interpretation:

The synthesis of ether, tert−butyl isopropyl ether, using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms ether.

Answer 12

Interpretation Introduction

(d)

Interpretation:

The synthesis of dibutyl ether using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms an ether.

Answer 13

Interpretation Introduction

(d)

Interpretation:

The synthesis of dibutyl ether using either alcohol dehydration or alkene addition is to be stated.

Concept introduction:

The treatment of alcohols with dilute sulfuric acid in the presence of excess ethanol leads to the formation of ether as a product. In this reaction, a stable carbocation is formed as an intermediate after the removal of a water molecule. Therefore, the carbocation attacked by the ethanol group forms an ether.

Answer 14

Expert Solution & Answer

Answer 15

Expert Solution & Answer

Answer 16

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 17

Ch. 11 - Prob. 11.1P Ch. 11 - Prob. 11.2P Ch. 11 - Prob. 11.3P Ch. 11 - Prob. 11.4P Ch. 11 - Prob. 11.5P Ch. 11 - Prob. 11.6P Ch. 11 - Prob. 11.7P Ch. 11 - Prob. 11.8P Ch. 11 - Prob. 11.9P Ch. 11 - Prob. 11.10P

Solution Summary: The author explains the synthesis of ether using either alcohol dehydration or alkene addition.

Concept explainers

Want to see the full answer?

Chapter 11 Solutions