The mechanism for reaction between benzene and given electrophile should be identified. Concept Introduction: Mechanism for electrophilic aromatic substitution is as follows, 1. First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate. 2. The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

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Answer 1

Question

Chapter 7.17, Problem 29P

(a)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1. First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2. The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

(b)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

(c)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

(d)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

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For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. ? Will the first MgBr product that forms in this reaction create a new CC bond? olo ? OH جمله O Yes Ⓒ No MgCl ? Will the first product that forms in this reaction create a new CC bond? Click and drag to start drawing a structure. Yes No X ☐ : ☐ टे PH

Assign all the protons

PROPOSE REACTION MECHANISM FOR ACID-CATALYZED REACTION OF 3-PENTANONE WITH DIMETHYLAMINE

Answer 2

Question

Chapter 7.17, Problem 29P

(a)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1. First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2. The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

(b)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

(c)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

(d)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

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Answer 3

Question

Chapter 7.17, Problem 29P

(a)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1. First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2. The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

(b)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

(c)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

(d)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

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Answer 4

Question

Chapter 7.17, Problem 29P

(a)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1. First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2. The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

(b)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

(c)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

(d)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

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Answer 5

Chapter 7.17, Problem 29P

(a)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1. First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2. The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

(b)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

(c)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

(d)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

Answer 6

Chapter 7.17, Problem 29P

(a)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1. First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2. The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

Answer 7

Chapter 7.17, Problem 29P

(a)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1. First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2. The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

Answer 8

(b)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

Answer 9

(b)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate which then electrons again move into the ring regaining its aromaticity.

Answer 10

(c)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

Answer 11

(c)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

Answer 12

(d)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

Answer 13

(d)

Interpretation Introduction

Interpretation:

The mechanism for reaction between benzene and given electrophile should be identified.

Concept Introduction:

Mechanism for electrophilic aromatic substitution is as follows,

1 First, electrophile gets added to the carbon–carbon double bond in benzene which then results to form carbocation intermediate.

2 The base removes the proton present in carbocation intermediate in which electrons present in C-H bond again moves into the ring regaining its aromaticity results in the formation of product.

Answer 14

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Answer 15

Expert Solution & Answer

Answer 16

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Answer 17

Ch. 7.4 - Prob. 1P Ch. 7.5 - Prob. 3P Ch. 7.6 - a. Predict the relative bond lengths of the three...Ch. 7.6 - Prob. 5P Ch. 7.6 - Prob. 6P Ch. 7.7 - Prob. 7P Ch. 7.7 - Prob. 8P Ch. 7.7 - Prob. 9P Ch. 7.7 - Prob. 10P Ch. 7.8 - Which member of each pair is the stronger acid? a....

Solution Summary: The author explains the mechanism for reaction between benzene and given electrophile.

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