The product of light-initiated reaction of cyclopentene with NBS in CCl 4 is to be predicted. Concept introduction: NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Question

Want to see the full answer?

Answer 1

Question

Chapter 15.7, Problem 15.11P

(a)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of cyclopentene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

(b)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of 2,3-dimethylbut-2-ene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

(c)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of toluene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

I have some reactions here for which I need to predict the products. Can you help me solve them and rewrite the equations, as well as identify the type of reaction? Please explain it to me.I have some reactions here for which I need to predict the products. Can you help me solve them and rewrite the equations, as well as identify the type of reaction? Please explain it to m

Draw the major product of this reaction. Ignore inorganic byproducts. Problem 17 of 35 1. CH3CH2Li O H 2. Neutralizing work-up @ Atoms, Bonds and Rings Draw or tap a new bo

Will this convert the C=O to an alcohol? Or does its participation in the carboxy group prevent that from happening?

Answer 2

Question

Chapter 15.7, Problem 15.11P

(a)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of cyclopentene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

(b)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of 2,3-dimethylbut-2-ene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

(c)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of toluene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Chapter 15.7, Problem 15.11P

(a)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of cyclopentene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

(b)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of 2,3-dimethylbut-2-ene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

(c)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of toluene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Chapter 15.7, Problem 15.11P

(a)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of cyclopentene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

(b)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of 2,3-dimethylbut-2-ene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

(c)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of toluene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 5

Chapter 15.7, Problem 15.11P

(a)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of cyclopentene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

(b)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of 2,3-dimethylbut-2-ene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

(c)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of toluene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Answer 6

Chapter 15.7, Problem 15.11P

(a)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of cyclopentene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Answer 7

Chapter 15.7, Problem 15.11P

(a)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of cyclopentene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Answer 8

(b)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of 2,3-dimethylbut-2-ene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Answer 9

(b)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of 2,3-dimethylbut-2-ene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Answer 10

(c)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of toluene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Answer 11

(c)

Interpretation Introduction

Interpretation:

The product of light-initiated reaction of toluene with NBS in CCl4 is to be predicted.

Concept introduction:

NBS is a source of bromine atom which abstract hydrogen atom from alkene at allylic position and occupy that position when it is exposed to light. The mechanism of the reaction involves the formation of allylic radical which shows resonating structures due to presence of adjacent double bond.

Answer 12

Expert Solution & Answer

Answer 13

Expert Solution & Answer

Answer 14

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 15

Ch. 15.2 - Prob. 15.1P Ch. 15.2 - Prob. 15.2P Ch. 15.2 - Prob. 15.3P Ch. 15.4 - Prob. 15.4P Ch. 15.4 - Prob. 15.5P Ch. 15.5 - Treatment of an alkyl halide with AgNO3 in alcohol...Ch. 15.5 - Propose a mechanism for each reaction, showing...Ch. 15.6 - When Br2 is added to buta-1,3-diene at 15 C, the...Ch. 15.7 - Prob. 15.9P Ch. 15.7 - When N-bromosuccinimide is added to hex-1-ene in...

Want to see the full answer?

Chapter 15 Solutions