The benzophenone n-Π* triplet T1 without having benzophenone pass through its first singlet stateneeds to be determined. Concept Introduction: In the singlet state; the orientation of electrons has the same spin while in the triplet state; the orientation of electrons has the opposite spin.

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Answer 1

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Chapter 54, Problem 1Q

Interpretation Introduction

Interpretation:

The benzophenone n-Π* triplet T1 without having benzophenone pass through its first singlet stateneeds to be determined.

Concept Introduction:

In the singlet state; the orientation of electrons has the same spin while in the triplet state; the orientation of electrons has the opposite spin.

Expert Solution & Answer

Explanation of Solution

The reaction between benzophenone and isopropyl alcohol is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 1

The quantum yield for the given reaction is a unity which states that each molecule of excited benzophenone gives one molecule of benzo pinacol. In the given reaction; fluorescence is not observed, a triplet excited state is involved. n-Π* triplet excited state takes a hydrogen atom from isopropanol.

The mechanism of the given reaction is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 2

Where,

S0 = singlet ground state

S1 = first singlet excited state

T1 = first triplet excited state

ISC = intersystem crossing

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 3

According to the mechanism; it shows that the singlet excited state of benzophenone gores through intersystem crossing to triplet state very readily. Therefore, it is the triplet state that is involved.

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b) Certain cyclic compounds are known to be conformationally similar to carbohydrates, although they are not themselves carbohydrates. One example is Compound C shown below, which could be imagined as adopting four possible conformations. In reality, however, only one of these is particularly stable. Circle the conformation you expect to be the most stable, and provide an explanation to justify your choice. For your explanation to be both convincing and correct, it must contain not only words, but also "cartoon" orbital drawings contrasting the four structures. Compound C Possible conformations (circle one): Дет

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Answer 2

Question

Chapter 54, Problem 1Q

Interpretation Introduction

Interpretation:

The benzophenone n-Π* triplet T1 without having benzophenone pass through its first singlet stateneeds to be determined.

Concept Introduction:

In the singlet state; the orientation of electrons has the same spin while in the triplet state; the orientation of electrons has the opposite spin.

Expert Solution & Answer

Explanation of Solution

The reaction between benzophenone and isopropyl alcohol is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 1

The quantum yield for the given reaction is a unity which states that each molecule of excited benzophenone gives one molecule of benzo pinacol. In the given reaction; fluorescence is not observed, a triplet excited state is involved. n-Π* triplet excited state takes a hydrogen atom from isopropanol.

The mechanism of the given reaction is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 2

Where,

S0 = singlet ground state

S1 = first singlet excited state

T1 = first triplet excited state

ISC = intersystem crossing

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 3

According to the mechanism; it shows that the singlet excited state of benzophenone gores through intersystem crossing to triplet state very readily. Therefore, it is the triplet state that is involved.

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Answer 3

Question

Chapter 54, Problem 1Q

Interpretation Introduction

Interpretation:

The benzophenone n-Π* triplet T1 without having benzophenone pass through its first singlet stateneeds to be determined.

Concept Introduction:

In the singlet state; the orientation of electrons has the same spin while in the triplet state; the orientation of electrons has the opposite spin.

Expert Solution & Answer

Explanation of Solution

The reaction between benzophenone and isopropyl alcohol is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 1

The quantum yield for the given reaction is a unity which states that each molecule of excited benzophenone gives one molecule of benzo pinacol. In the given reaction; fluorescence is not observed, a triplet excited state is involved. n-Π* triplet excited state takes a hydrogen atom from isopropanol.

The mechanism of the given reaction is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 2

Where,

S0 = singlet ground state

S1 = first singlet excited state

T1 = first triplet excited state

ISC = intersystem crossing

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 3

According to the mechanism; it shows that the singlet excited state of benzophenone gores through intersystem crossing to triplet state very readily. Therefore, it is the triplet state that is involved.

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Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!

Answer 4

Question

Chapter 54, Problem 1Q

Interpretation Introduction

Interpretation:

The benzophenone n-Π* triplet T1 without having benzophenone pass through its first singlet stateneeds to be determined.

Concept Introduction:

In the singlet state; the orientation of electrons has the same spin while in the triplet state; the orientation of electrons has the opposite spin.

Expert Solution & Answer

Explanation of Solution

The reaction between benzophenone and isopropyl alcohol is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 1

The quantum yield for the given reaction is a unity which states that each molecule of excited benzophenone gives one molecule of benzo pinacol. In the given reaction; fluorescence is not observed, a triplet excited state is involved. n-Π* triplet excited state takes a hydrogen atom from isopropanol.

The mechanism of the given reaction is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 2

Where,

S0 = singlet ground state

S1 = first singlet excited state

T1 = first triplet excited state

ISC = intersystem crossing

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 3

According to the mechanism; it shows that the singlet excited state of benzophenone gores through intersystem crossing to triplet state very readily. Therefore, it is the triplet state that is involved.

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Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!

Answer 5

Chapter 54, Problem 1Q

Interpretation Introduction

Interpretation:

The benzophenone n-Π* triplet T1 without having benzophenone pass through its first singlet stateneeds to be determined.

Concept Introduction:

In the singlet state; the orientation of electrons has the same spin while in the triplet state; the orientation of electrons has the opposite spin.

Expert Solution & Answer

Explanation of Solution

The reaction between benzophenone and isopropyl alcohol is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 1

The quantum yield for the given reaction is a unity which states that each molecule of excited benzophenone gives one molecule of benzo pinacol. In the given reaction; fluorescence is not observed, a triplet excited state is involved. n-Π* triplet excited state takes a hydrogen atom from isopropanol.

The mechanism of the given reaction is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 2

Where,

S0 = singlet ground state

S1 = first singlet excited state

T1 = first triplet excited state

ISC = intersystem crossing

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 3

According to the mechanism; it shows that the singlet excited state of benzophenone gores through intersystem crossing to triplet state very readily. Therefore, it is the triplet state that is involved.

Answer 6

Chapter 54, Problem 1Q

Interpretation Introduction

Interpretation:

The benzophenone n-Π* triplet T1 without having benzophenone pass through its first singlet stateneeds to be determined.

Concept Introduction:

In the singlet state; the orientation of electrons has the same spin while in the triplet state; the orientation of electrons has the opposite spin.

Expert Solution & Answer

Explanation of Solution

The reaction between benzophenone and isopropyl alcohol is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 1

The quantum yield for the given reaction is a unity which states that each molecule of excited benzophenone gives one molecule of benzo pinacol. In the given reaction; fluorescence is not observed, a triplet excited state is involved. n-Π* triplet excited state takes a hydrogen atom from isopropanol.

The mechanism of the given reaction is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 2

Where,

S0 = singlet ground state

S1 = first singlet excited state

T1 = first triplet excited state

ISC = intersystem crossing

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 3

According to the mechanism; it shows that the singlet excited state of benzophenone gores through intersystem crossing to triplet state very readily. Therefore, it is the triplet state that is involved.

Answer 7

Chapter 54, Problem 1Q

Interpretation Introduction

Interpretation:

The benzophenone n-Π* triplet T1 without having benzophenone pass through its first singlet stateneeds to be determined.

Concept Introduction:

In the singlet state; the orientation of electrons has the same spin while in the triplet state; the orientation of electrons has the opposite spin.

Answer 8

Expert Solution & Answer

Explanation of Solution

The reaction between benzophenone and isopropyl alcohol is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 1

The quantum yield for the given reaction is a unity which states that each molecule of excited benzophenone gives one molecule of benzo pinacol. In the given reaction; fluorescence is not observed, a triplet excited state is involved. n-Π* triplet excited state takes a hydrogen atom from isopropanol.

The mechanism of the given reaction is shown below:

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 2

Where,

S0 = singlet ground state

S1 = first singlet excited state

T1 = first triplet excited state

ISC = intersystem crossing

EBK A SMALL SCALE APPROACH TO ORGANIC L, Chapter 54, Problem 1Q , additional homework tip 3

According to the mechanism; it shows that the singlet excited state of benzophenone gores through intersystem crossing to triplet state very readily. Therefore, it is the triplet state that is involved.

Answer 9

Expert Solution & Answer

Answer 10

Expert Solution & Answer

Answer 11

Ch. 54 - Prob. 1Q

The benzophenone n-Π* triplet T1 without having benzophenone pass through its first singlet stateneeds to be determined. Concept Introduction: In the singlet state; the orientation of electrons has the same spin while in the triplet state; the orientation of electrons has the opposite spin.

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