(a) Interpretation: The compound among the thiophene and divinyl sulfide that shows NMR absorptions with greater chemical shifts is to be stated. Concept introduction: Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

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Answer 1

Question

Chapter 16, Problem 16.4P

Interpretation Introduction

(a)

Interpretation:

The compound among the thiophene and divinyl sulfide that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

Interpretation Introduction

(b)

Interpretation:

The compound among the cyclohex-1, 4-diene and benzene that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

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Answer 2

Question

Chapter 16, Problem 16.4P

Interpretation Introduction

(a)

Interpretation:

The compound among the thiophene and divinyl sulfide that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

Interpretation Introduction

(b)

Interpretation:

The compound among the cyclohex-1, 4-diene and benzene that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

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Answer 3

Question

Chapter 16, Problem 16.4P

Interpretation Introduction

(a)

Interpretation:

The compound among the thiophene and divinyl sulfide that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

Interpretation Introduction

(b)

Interpretation:

The compound among the cyclohex-1, 4-diene and benzene that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

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Answer 4

Question

Chapter 16, Problem 16.4P

Interpretation Introduction

(a)

Interpretation:

The compound among the thiophene and divinyl sulfide that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

Interpretation Introduction

(b)

Interpretation:

The compound among the cyclohex-1, 4-diene and benzene that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

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Answer 5

Chapter 16, Problem 16.4P

Interpretation Introduction

(a)

Interpretation:

The compound among the thiophene and divinyl sulfide that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

Interpretation Introduction

(b)

Interpretation:

The compound among the cyclohex-1, 4-diene and benzene that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

Answer 6

Chapter 16, Problem 16.4P

Interpretation Introduction

(a)

Interpretation:

The compound among the thiophene and divinyl sulfide that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

Answer 7

Chapter 16, Problem 16.4P

Interpretation Introduction

(a)

Interpretation:

The compound among the thiophene and divinyl sulfide that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

Answer 8

Interpretation Introduction

(b)

Interpretation:

The compound among the cyclohex-1, 4-diene and benzene that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

Answer 9

Interpretation Introduction

(b)

Interpretation:

The compound among the cyclohex-1, 4-diene and benzene that shows NMR absorptions with greater chemical shifts is to be stated.

Concept introduction:

Many nuclei and electrons have spin. Due to this, spin magnetic moment arises. The energy of this magnetic moment depends on the orientation of the applied magnetic field. In NMR spectroscopy, every nucleus has a spin. There is an angular momentum related to the spin. The difference between its resonance frequency and that of the reference standard is known as the chemical shift of a nucleus. Tetramethylsilane (TMS) is taken as reference.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 16 - Prob. 16.1P Ch. 16 - Prob. 16.2P Ch. 16 - Prob. 16.3P Ch. 16 - Prob. 16.4P Ch. 16 - Prob. 16.5P Ch. 16 - Prob. 16.6P Ch. 16 - Prob. 16.7P Ch. 16 - Prob. 16.8P Ch. 16 - Prob. 16.9P Ch. 16 - Prob. 16.10P

Solution Summary: The author states that thiophene shows NMR absorptions with greater chemical shifts than divinyl sulfide.

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