A compound X with the molecular formula C 11 H 24 O 3 and no O − H stretching absorption in its IR spectrum is to be identified on the basis of given information. Concept introduction: NMR spectroscopy is a technique used to determine a unique structure of the compounds. It identifies the carbon-hydrogen bonding of an organic compound. A hydrogen atom is called as a proton in the NMR spectroscopy. The number of NMR signal in a compound is equal to the number of chemically non-equivalent protons present in that compound. The more the shielded proton lesser will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region or vice versa.

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Answer 1

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Chapter 13, Problem 13.17P

Interpretation Introduction

Interpretation:

A compound X with the molecular formula C11H24O3 and no O−H stretching absorption in its IR spectrum is to be identified on the basis of given information.

Concept introduction:

NMR spectroscopy is a technique used to determine a unique structure of the compounds. It identifies the carbon-hydrogen bonding of an organic compound. A hydrogen atom is called as a proton in the NMR spectroscopy.

The number of NMR signal in a compound is equal to the number of chemically non-equivalent protons present in that compound. The more the shielded proton lesser will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region or vice versa.

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please provide the structure for this problem, thank you

Answer 2

Question

Chapter 13, Problem 13.17P

Interpretation Introduction

Interpretation:

A compound X with the molecular formula C11H24O3 and no O−H stretching absorption in its IR spectrum is to be identified on the basis of given information.

Concept introduction:

NMR spectroscopy is a technique used to determine a unique structure of the compounds. It identifies the carbon-hydrogen bonding of an organic compound. A hydrogen atom is called as a proton in the NMR spectroscopy.

The number of NMR signal in a compound is equal to the number of chemically non-equivalent protons present in that compound. The more the shielded proton lesser will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region or vice versa.

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Answer 3

Question

Chapter 13, Problem 13.17P

Interpretation Introduction

Interpretation:

A compound X with the molecular formula C11H24O3 and no O−H stretching absorption in its IR spectrum is to be identified on the basis of given information.

Concept introduction:

NMR spectroscopy is a technique used to determine a unique structure of the compounds. It identifies the carbon-hydrogen bonding of an organic compound. A hydrogen atom is called as a proton in the NMR spectroscopy.

The number of NMR signal in a compound is equal to the number of chemically non-equivalent protons present in that compound. The more the shielded proton lesser will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region or vice versa.

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Answer 4

Question

Chapter 13, Problem 13.17P

Interpretation Introduction

Interpretation:

A compound X with the molecular formula C11H24O3 and no O−H stretching absorption in its IR spectrum is to be identified on the basis of given information.

Concept introduction:

NMR spectroscopy is a technique used to determine a unique structure of the compounds. It identifies the carbon-hydrogen bonding of an organic compound. A hydrogen atom is called as a proton in the NMR spectroscopy.

The number of NMR signal in a compound is equal to the number of chemically non-equivalent protons present in that compound. The more the shielded proton lesser will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region or vice versa.

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Answer 5

Chapter 13, Problem 13.17P

Interpretation Introduction

Interpretation:

A compound X with the molecular formula C11H24O3 and no O−H stretching absorption in its IR spectrum is to be identified on the basis of given information.

Concept introduction:

NMR spectroscopy is a technique used to determine a unique structure of the compounds. It identifies the carbon-hydrogen bonding of an organic compound. A hydrogen atom is called as a proton in the NMR spectroscopy.

The number of NMR signal in a compound is equal to the number of chemically non-equivalent protons present in that compound. The more the shielded proton lesser will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region or vice versa.

Answer 6

Chapter 13, Problem 13.17P

Interpretation Introduction

Interpretation:

A compound X with the molecular formula C11H24O3 and no O−H stretching absorption in its IR spectrum is to be identified on the basis of given information.

Concept introduction:

NMR spectroscopy is a technique used to determine a unique structure of the compounds. It identifies the carbon-hydrogen bonding of an organic compound. A hydrogen atom is called as a proton in the NMR spectroscopy.

The number of NMR signal in a compound is equal to the number of chemically non-equivalent protons present in that compound. The more the shielded proton lesser will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region or vice versa.

Answer 7

Chapter 13, Problem 13.17P

Interpretation Introduction

Interpretation:

A compound X with the molecular formula C11H24O3 and no O−H stretching absorption in its IR spectrum is to be identified on the basis of given information.

Concept introduction:

NMR spectroscopy is a technique used to determine a unique structure of the compounds. It identifies the carbon-hydrogen bonding of an organic compound. A hydrogen atom is called as a proton in the NMR spectroscopy.

The number of NMR signal in a compound is equal to the number of chemically non-equivalent protons present in that compound. The more the shielded proton lesser will be its chemical shift value and the corresponding signal will be produced at the right-hand side or lower frequency region or vice versa.

Answer 8

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Answer 10

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Answer 11

Ch. 13 - Prob. 13.1P Ch. 13 - Prob. 13.2P Ch. 13 - Prob. 13.3P Ch. 13 - Prob. 13.4P Ch. 13 - Prob. 13.5P Ch. 13 - Prob. 13.6P Ch. 13 - Prob. 13.7P Ch. 13 - Prob. 13.8P Ch. 13 - Prob. 13.9P Ch. 13 - Prob. 13.10P

Solution Summary: The author explains how NMR spectroscopy identifies the carbon-hydrogen bonding of an organic compound.

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