(a) Interpretation: The diene that would react with ethene to produce the given compound is to be drawn. Concept introduction: The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

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Answer 1

Question

Chapter 24, Problem 24.29P

Interpretation Introduction

(a)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(b)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(c)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(d)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

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2. 200 LOD For an unknown compound with a molecular ion of 101 m/z: a. Use the molecular ion to propose at least two molecular formulas. (show your work) b. What is the DU for each of your possible formulas? (show your work) C. Solve the structure and assign each of the following spectra. 8 6 4 2 (ppm) 150 100 50 ō (ppm) 4000 3000 2000 1500 1000 500 HAVENUMBERI-11

Complete the spectroscopy with structure

Answer 2

Question

Chapter 24, Problem 24.29P

Interpretation Introduction

(a)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(b)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(c)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(d)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

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Answer 3

Question

Chapter 24, Problem 24.29P

Interpretation Introduction

(a)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(b)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(c)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(d)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

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Answer 4

Question

Chapter 24, Problem 24.29P

Interpretation Introduction

(a)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(b)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(c)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(d)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

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Answer 5

Chapter 24, Problem 24.29P

Interpretation Introduction

(a)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(b)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(c)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Interpretation Introduction

(d)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Answer 6

Chapter 24, Problem 24.29P

Interpretation Introduction

(a)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Answer 7

Chapter 24, Problem 24.29P

Interpretation Introduction

(a)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Answer 10

Interpretation Introduction

(c)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Answer 11

Interpretation Introduction

(c)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Answer 12

Interpretation Introduction

(d)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Answer 13

Interpretation Introduction

(d)

Interpretation:

The diene that would react with ethene to produce the given compound is to be drawn.

Concept introduction:

The Diels-Alder reaction is the cycloaddition of diene and dienophile. The diene has a pair of conjugate double and contributes its 4π electrons. The dienophile has single double bond and contributes its 2π electrons. These six electrons must flow in a cyclic fashion. Thus, the reaction proceeds through a cyclic transition state, which makes it a pericyclic reaction. Therefore, the Diels-Alder reaction is called [4+2] cycloaddition. The carbons from the diene have C=C bond in the six membered ring product.

Answer 14

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Answer 15

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Answer 16

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Answer 17

Ch. 24 - Prob. 24.1P Ch. 24 - Prob. 24.2P Ch. 24 - Prob. 24.3P Ch. 24 - Prob. 24.4P Ch. 24 - Prob. 24.5P Ch. 24 - Prob. 24.6P Ch. 24 - Prob. 24.7P Ch. 24 - Prob. 24.8P Ch. 24 - Prob. 24.9P Ch. 24 - Prob. 24.10P

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Chapter 24 Solutions