The trend of reactivity for Cyclopentadiene, 1,3-cyclohexadiene and 1,3-cycloheptadiene are rapidly reactive, mild reactive and unreactive respectively in Diels-Alder reaction should be explained. Concept introduction: Cycloaddition reaction is a concerted addition reaction of two reactants to form a ring; in which two π-bonds are converted to two σ-bonds . Diels-Alder reaction is a [ 4+2 ] cycloaddition reaction, in which a π-system having four atoms (diene) and a π-system having two atoms (dienophile) are undergoing in cycloaddition reaction and producing a substituted cyclohexene . The mechanism of the ring formation in the Diels-Alder reaction is drawn by using three arrows representing the shifting of π-bonds in the two π-systems in a clockwise or counter clockwise fashion, so that the ring formation will take place. The more steric hindrance in the dienes will be less reactive for the Diels-Alder reaction.

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Answer 1

Question

Chapter 17, Problem 48PP

Interpretation Introduction

Interpretation:

The trend of reactivity for Cyclopentadiene, 1,3-cyclohexadiene and 1,3-cycloheptadiene are rapidly reactive, mild reactive and unreactive respectively in Diels-Alder reaction should be explained.

Concept introduction:

Cycloaddition reaction is a concerted addition reaction of two reactants to form a ring; in which two π-bonds are converted to two σ-bonds.

Diels-Alder reaction is a [4+2] cycloaddition reaction, in which a π-system having four atoms (diene) and a π-system having two atoms (dienophile) are undergoing in cycloaddition reaction and producing a substituted cyclohexene.

The mechanism of the ring formation in the Diels-Alder reaction is drawn by using three arrows representing the shifting of π-bonds in the two π-systems in a clockwise or counter clockwise fashion, so that the ring formation will take place.

The more steric hindrance in the dienes will be less reactive for the Diels-Alder reaction.

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Answer 2

Question

Chapter 17, Problem 48PP

Interpretation Introduction

Interpretation:

The trend of reactivity for Cyclopentadiene, 1,3-cyclohexadiene and 1,3-cycloheptadiene are rapidly reactive, mild reactive and unreactive respectively in Diels-Alder reaction should be explained.

Concept introduction:

Cycloaddition reaction is a concerted addition reaction of two reactants to form a ring; in which two π-bonds are converted to two σ-bonds.

Diels-Alder reaction is a [4+2] cycloaddition reaction, in which a π-system having four atoms (diene) and a π-system having two atoms (dienophile) are undergoing in cycloaddition reaction and producing a substituted cyclohexene.

The mechanism of the ring formation in the Diels-Alder reaction is drawn by using three arrows representing the shifting of π-bonds in the two π-systems in a clockwise or counter clockwise fashion, so that the ring formation will take place.

The more steric hindrance in the dienes will be less reactive for the Diels-Alder reaction.

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Answer 3

Question

Chapter 17, Problem 48PP

Interpretation Introduction

Interpretation:

The trend of reactivity for Cyclopentadiene, 1,3-cyclohexadiene and 1,3-cycloheptadiene are rapidly reactive, mild reactive and unreactive respectively in Diels-Alder reaction should be explained.

Concept introduction:

Cycloaddition reaction is a concerted addition reaction of two reactants to form a ring; in which two π-bonds are converted to two σ-bonds.

Diels-Alder reaction is a [4+2] cycloaddition reaction, in which a π-system having four atoms (diene) and a π-system having two atoms (dienophile) are undergoing in cycloaddition reaction and producing a substituted cyclohexene.

The mechanism of the ring formation in the Diels-Alder reaction is drawn by using three arrows representing the shifting of π-bonds in the two π-systems in a clockwise or counter clockwise fashion, so that the ring formation will take place.

The more steric hindrance in the dienes will be less reactive for the Diels-Alder reaction.

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Answer 4

Question

Chapter 17, Problem 48PP

Interpretation Introduction

Interpretation:

The trend of reactivity for Cyclopentadiene, 1,3-cyclohexadiene and 1,3-cycloheptadiene are rapidly reactive, mild reactive and unreactive respectively in Diels-Alder reaction should be explained.

Concept introduction:

Cycloaddition reaction is a concerted addition reaction of two reactants to form a ring; in which two π-bonds are converted to two σ-bonds.

Diels-Alder reaction is a [4+2] cycloaddition reaction, in which a π-system having four atoms (diene) and a π-system having two atoms (dienophile) are undergoing in cycloaddition reaction and producing a substituted cyclohexene.

The mechanism of the ring formation in the Diels-Alder reaction is drawn by using three arrows representing the shifting of π-bonds in the two π-systems in a clockwise or counter clockwise fashion, so that the ring formation will take place.

The more steric hindrance in the dienes will be less reactive for the Diels-Alder reaction.

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Answer 5

Chapter 17, Problem 48PP

Interpretation Introduction

Interpretation:

The trend of reactivity for Cyclopentadiene, 1,3-cyclohexadiene and 1,3-cycloheptadiene are rapidly reactive, mild reactive and unreactive respectively in Diels-Alder reaction should be explained.

Concept introduction:

Cycloaddition reaction is a concerted addition reaction of two reactants to form a ring; in which two π-bonds are converted to two σ-bonds.

Diels-Alder reaction is a [4+2] cycloaddition reaction, in which a π-system having four atoms (diene) and a π-system having two atoms (dienophile) are undergoing in cycloaddition reaction and producing a substituted cyclohexene.

The mechanism of the ring formation in the Diels-Alder reaction is drawn by using three arrows representing the shifting of π-bonds in the two π-systems in a clockwise or counter clockwise fashion, so that the ring formation will take place.

The more steric hindrance in the dienes will be less reactive for the Diels-Alder reaction.

Answer 6

Chapter 17, Problem 48PP

Interpretation Introduction

Interpretation:

The trend of reactivity for Cyclopentadiene, 1,3-cyclohexadiene and 1,3-cycloheptadiene are rapidly reactive, mild reactive and unreactive respectively in Diels-Alder reaction should be explained.

Concept introduction:

Cycloaddition reaction is a concerted addition reaction of two reactants to form a ring; in which two π-bonds are converted to two σ-bonds.

Diels-Alder reaction is a [4+2] cycloaddition reaction, in which a π-system having four atoms (diene) and a π-system having two atoms (dienophile) are undergoing in cycloaddition reaction and producing a substituted cyclohexene.

The mechanism of the ring formation in the Diels-Alder reaction is drawn by using three arrows representing the shifting of π-bonds in the two π-systems in a clockwise or counter clockwise fashion, so that the ring formation will take place.

The more steric hindrance in the dienes will be less reactive for the Diels-Alder reaction.

Answer 7

Chapter 17, Problem 48PP

Interpretation Introduction

Interpretation:

The trend of reactivity for Cyclopentadiene, 1,3-cyclohexadiene and 1,3-cycloheptadiene are rapidly reactive, mild reactive and unreactive respectively in Diels-Alder reaction should be explained.

Concept introduction:

Cycloaddition reaction is a concerted addition reaction of two reactants to form a ring; in which two π-bonds are converted to two σ-bonds.

Diels-Alder reaction is a [4+2] cycloaddition reaction, in which a π-system having four atoms (diene) and a π-system having two atoms (dienophile) are undergoing in cycloaddition reaction and producing a substituted cyclohexene.

The mechanism of the ring formation in the Diels-Alder reaction is drawn by using three arrows representing the shifting of π-bonds in the two π-systems in a clockwise or counter clockwise fashion, so that the ring formation will take place.

The more steric hindrance in the dienes will be less reactive for the Diels-Alder reaction.

Answer 8

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Answer 9

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Answer 10

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Answer 11

Ch. 17.1 - Prob. 1CC Ch. 17.2 - Prob. 2CC Ch. 17.2 - Prob. 3CC Ch. 17.2 - Prob. 4CC Ch. 17.2 - Prob. 5CC Ch. 17.3 - Prob. 6CC Ch. 17.4 - Prob. 1LTS Ch. 17.4 - Prob. 7PTS Ch. 17.4 - Prob. 8ATS Ch. 17.4 - Prob. 9ATS

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