(a) Interpretation: How the given compound can be synthesized from two different alkenes is to be shown. Concept introduction: Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Question

=Naming benzene derivatives Name these organic compounds: structure C1 CH3 name ☐ CH3 ப C1 × ☐

Answer 1

Question

Chapter 11, Problem 11.5P

Interpretation Introduction

(a)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Interpretation Introduction

(b)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Interpretation Introduction

(c)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

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=Naming benzene derivatives Name these organic compounds: structure C1 CH3 name ☐ CH3 ப C1 × ☐

Blocking Group are use to put 2 large sterically repulsive group ortho. Show the correct sequence toconnect the reagent to product with the highest yield possible. * see image **NOTE: The compound on the left is the starting point, and the compound on the right is the final product. Please show the steps in between to get from start to final, please. These are not two different compounds that need to be worked.

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Answer 2

Question

Chapter 11, Problem 11.5P

Interpretation Introduction

(a)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Interpretation Introduction

(b)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Interpretation Introduction

(c)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

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Answer 3

Question

Chapter 11, Problem 11.5P

Interpretation Introduction

(a)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Interpretation Introduction

(b)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Interpretation Introduction

(c)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

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Answer 4

Question

Chapter 11, Problem 11.5P

Interpretation Introduction

(a)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Interpretation Introduction

(b)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Interpretation Introduction

(c)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

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Answer 5

Chapter 11, Problem 11.5P

Interpretation Introduction

(a)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Interpretation Introduction

(b)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Interpretation Introduction

(c)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Answer 6

Chapter 11, Problem 11.5P

Interpretation Introduction

(a)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Answer 7

Chapter 11, Problem 11.5P

Interpretation Introduction

(a)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Answer 8

Interpretation Introduction

(b)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Answer 9

Interpretation Introduction

(b)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Answer 10

Interpretation Introduction

(c)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Answer 11

Interpretation Introduction

(c)

Interpretation:

How the given compound can be synthesized from two different alkenes is to be shown.

Concept introduction:

Bronsted acids add across a C - C double bond. The mechanism involves the electrophilic addition of the acid’s proton to the electron-rich π bond in step one. The proton adds to the less substituted carbon of the initial double bond so that the most substituted, and hence, the most stable carbocation forms. Step two is a coordination step in which the conjugate base forms a bond to the carbocation. The major product of an electrophilic addition of a Bronsted acid to an alkene is the one that proceeds through the more stable carbocation intermediate.

Answer 12

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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 how Bronsted acids add across a C - C double bond. The proton adds to the less substituted carbon of the initial bond so that the most stable carboc

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