The alkyl halide given is prepared by addition of HBr to two different alkenes . The structures of both alkenes are to be drawn. Concept introduction: In electrophilic addition reactions the first step involves the attack of the π electrons of the double bond on the positively polarized hydrogen atom of the hydrogen halide to give a carbocation as the product with the elimination of a halide ion. In the second step the carbocation reacts with the halide ion to give the product. To draw: The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr.

Question

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Answer 1

Question

Chapter 6.SE, Problem 14VC

Interpretation Introduction

Interpretation:

The alkyl halide given is prepared by addition of HBr to two different alkenes. The structures of both alkenes are to be drawn.

Concept introduction:

In electrophilic addition reactions the first step involves the attack of the π electrons of the double bond on the positively polarized hydrogen atom of the hydrogen halide to give a carbocation as the product with the elimination of a halide ion. In the second step the carbocation reacts with the halide ion to give the product.

To draw:

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr.

Expert Solution & Answer

Answer to Problem 14VC

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

Organic Chemistry, Chapter 6.SE, Problem 14VC , additional homework tip 1

Explanation of Solution

Both 1-pentene and 2-pentene have double bonds in a position to yield the alkyl bromide when treated with HBr.

Conclusion

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

Organic Chemistry, Chapter 6.SE, Problem 14VC , additional homework tip 2

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2. The following carbocation is generated as an intermediate in the addition of H-Br to an alkene. Draw the structure of all possible alkenes that could have formed this intermediate.

Bent (D) Trigonal pyramidal 5. A student wishes to prepare ethyl acetate from the reaction of ethanol and acetic acid. To be successful, this reaction requires (A) an acidic catalyst. (C) an oxidizing agent. (B) a basic catalyst. (D) a reducing agent. 6. Which alkyl halide reacts most rapidly with aqueous sodium hydroxide solution? (A) CH₂Cl (B) CH₂I (C) (CH3)3CCH₂Cl (D) (CH3)3CCH₂I 57. How many isomers are there with the formula C6H₁4?

please answer both questions

Answer 2

Question

Chapter 6.SE, Problem 14VC

Interpretation Introduction

Interpretation:

The alkyl halide given is prepared by addition of HBr to two different alkenes. The structures of both alkenes are to be drawn.

Concept introduction:

In electrophilic addition reactions the first step involves the attack of the π electrons of the double bond on the positively polarized hydrogen atom of the hydrogen halide to give a carbocation as the product with the elimination of a halide ion. In the second step the carbocation reacts with the halide ion to give the product.

To draw:

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr.

Expert Solution & Answer

Answer to Problem 14VC

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

Explanation of Solution

Both 1-pentene and 2-pentene have double bonds in a position to yield the alkyl bromide when treated with HBr.

Conclusion

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

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Answer 3

Question

Chapter 6.SE, Problem 14VC

Interpretation Introduction

Interpretation:

The alkyl halide given is prepared by addition of HBr to two different alkenes. The structures of both alkenes are to be drawn.

Concept introduction:

In electrophilic addition reactions the first step involves the attack of the π electrons of the double bond on the positively polarized hydrogen atom of the hydrogen halide to give a carbocation as the product with the elimination of a halide ion. In the second step the carbocation reacts with the halide ion to give the product.

To draw:

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr.

Expert Solution & Answer

Answer to Problem 14VC

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

Explanation of Solution

Both 1-pentene and 2-pentene have double bonds in a position to yield the alkyl bromide when treated with HBr.

Conclusion

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

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Answer 4

Question

Chapter 6.SE, Problem 14VC

Interpretation Introduction

Interpretation:

The alkyl halide given is prepared by addition of HBr to two different alkenes. The structures of both alkenes are to be drawn.

Concept introduction:

In electrophilic addition reactions the first step involves the attack of the π electrons of the double bond on the positively polarized hydrogen atom of the hydrogen halide to give a carbocation as the product with the elimination of a halide ion. In the second step the carbocation reacts with the halide ion to give the product.

To draw:

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr.

Expert Solution & Answer

Answer to Problem 14VC

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

Explanation of Solution

Both 1-pentene and 2-pentene have double bonds in a position to yield the alkyl bromide when treated with HBr.

Conclusion

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

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Answer 5

Chapter 6.SE, Problem 14VC

Interpretation Introduction

Interpretation:

The alkyl halide given is prepared by addition of HBr to two different alkenes. The structures of both alkenes are to be drawn.

Concept introduction:

In electrophilic addition reactions the first step involves the attack of the π electrons of the double bond on the positively polarized hydrogen atom of the hydrogen halide to give a carbocation as the product with the elimination of a halide ion. In the second step the carbocation reacts with the halide ion to give the product.

To draw:

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr.

Expert Solution & Answer

Answer to Problem 14VC

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

Explanation of Solution

Both 1-pentene and 2-pentene have double bonds in a position to yield the alkyl bromide when treated with HBr.

Conclusion

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

Answer 6

Chapter 6.SE, Problem 14VC

Interpretation Introduction

Interpretation:

The alkyl halide given is prepared by addition of HBr to two different alkenes. The structures of both alkenes are to be drawn.

Concept introduction:

In electrophilic addition reactions the first step involves the attack of the π electrons of the double bond on the positively polarized hydrogen atom of the hydrogen halide to give a carbocation as the product with the elimination of a halide ion. In the second step the carbocation reacts with the halide ion to give the product.

To draw:

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr.

Expert Solution & Answer

Answer to Problem 14VC

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

Explanation of Solution

Both 1-pentene and 2-pentene have double bonds in a position to yield the alkyl bromide when treated with HBr.

Conclusion

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

Answer 7

Chapter 6.SE, Problem 14VC

Interpretation Introduction

Interpretation:

The alkyl halide given is prepared by addition of HBr to two different alkenes. The structures of both alkenes are to be drawn.

Concept introduction:

In electrophilic addition reactions the first step involves the attack of the π electrons of the double bond on the positively polarized hydrogen atom of the hydrogen halide to give a carbocation as the product with the elimination of a halide ion. In the second step the carbocation reacts with the halide ion to give the product.

To draw:

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr.

Answer 8

Expert Solution & Answer

Answer to Problem 14VC

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

Answer 9

Expert Solution & Answer

Answer 10

Expert Solution & Answer

Answer 11

Explanation of Solution

Both 1-pentene and 2-pentene have double bonds in a position to yield the alkyl bromide when treated with HBr.

Answer 12

Conclusion

The structures of two alkenes which will yield the alkyl halide given as product in an addition reaction with HBr are given below.

Answer 13

Ch. 6.1 - Prob. 1P Ch. 6.3 - Prob. 2P Ch. 6.3 - Using curved fishhook arrows, propose a mechanism...Ch. 6.4 - Prob. 4P Ch. 6.4 - An electrostatic potential map of boron...Ch. 6.5 - What product would you expect from reaction of...Ch. 6.5 - Reaction of HBr with 2-methylpropene yields...Ch. 6.6 - Prob. 8P Ch. 6.6 - Predict the products of the following polar...Ch. 6.7 - Which reaction is more energetically favored, one...

Concept explainers

Answer to Problem 14VC

Explanation of Solution

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Chapter 6 Solutions