The major product of the given reaction should be drawn. Concept introduction: In the presence of acid catalyst, this reaction takes place through partial S N 1 and partial S N 2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product. Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

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Answer 1

Question

Chapter 11.7, Problem 24P

(a)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(b)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial SN1 and partial SN2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(c)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(d)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

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Answer 2

Question

Chapter 11.7, Problem 24P

(a)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(b)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial SN1 and partial SN2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(c)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(d)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

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Answer 3

Question

Chapter 11.7, Problem 24P

(a)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(b)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial SN1 and partial SN2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(c)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(d)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

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Answer 4

Question

Chapter 11.7, Problem 24P

(a)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(b)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial SN1 and partial SN2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(c)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(d)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

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Answer 5

Chapter 11.7, Problem 24P

(a)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(b)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial SN1 and partial SN2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(c)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

(d)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

Answer 6

Chapter 11.7, Problem 24P

(a)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

Answer 7

Chapter 11.7, Problem 24P

(a)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

Answer 8

(b)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial SN1 and partial SN2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

Answer 9

(b)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial SN1 and partial SN2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

Answer 10

(c)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

Answer 11

(c)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

Answer 12

(d)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

Answer 13

(d)

Interpretation Introduction

Interpretation:

The major product of the given reaction should be drawn.

Concept introduction:

In the presence of acid catalyst, this reaction takes place through partial S_N1 and partial S_N2 pathway. Epoxides are reactive, Epoxides get protonated followed by alcohol attacks to the stable carbocation and form the product.

Epoxides are reactive, methoxide ion attacks the Epoxides in a less sterically hindered position which forms the alkoxide ion, and then it gets proton from alcohol which form the product.

Answer 14

Expert Solution & Answer

Answer 15

Expert Solution & Answer

Answer 16

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Answer 17

Ch. 11.1 - Why are NH3 and CH3NH2 no longer nucleophiles when...Ch. 11.1 - Prob. 2P Ch. 11.1 - Prob. 5P Ch. 11.2 - Prob. 7P Ch. 11.3 - Prob. 9P Ch. 11.3 - Show how 1-propanol can be converted into the...Ch. 11.4 - Which of the following alcohols dehydrates the...Ch. 11.4 - Prob. 12P Ch. 11.4 - Prob. 13P Ch. 11.4 - Propose a mechanism for each of the following...

Solution Summary: The author explains that the major product of the given reaction should be drawn in the presence of acid catalyst.

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