The structure of the given NMR spectrum and an explanation as to why the peaks around δ 1.65 and δ 3.75 show complex splitting even when these are not clean multiplets. Interpretation: The structure of the given NMR spectrum and an explanation as to why the peaks around δ 1.65 and δ 3.75 show complex splitting even when these are not clean multiplets is to be stated. 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.

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Answer 1

Question

Chapter 13.11B, Problem 13.21P

(a)

Interpretation Introduction

To determine: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets.

Interpretation: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets is to be stated.

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.

(b)

Interpretation Introduction

To determine: The reason that some of the protons are likely to be missed.

Interpretation: The reason that some of the protons are likely to be missed is to be stated.

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.

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Answer 2

Question

Chapter 13.11B, Problem 13.21P

(a)

Interpretation Introduction

To determine: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets.

Interpretation: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets is to be stated.

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.

(b)

Interpretation Introduction

To determine: The reason that some of the protons are likely to be missed.

Interpretation: The reason that some of the protons are likely to be missed is to be stated.

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.

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Answer 3

Question

Chapter 13.11B, Problem 13.21P

(a)

Interpretation Introduction

To determine: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets.

Interpretation: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets is to be stated.

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.

(b)

Interpretation Introduction

To determine: The reason that some of the protons are likely to be missed.

Interpretation: The reason that some of the protons are likely to be missed is to be stated.

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.

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Answer 4

Question

Chapter 13.11B, Problem 13.21P

(a)

Interpretation Introduction

To determine: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets.

Interpretation: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets is to be stated.

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.

(b)

Interpretation Introduction

To determine: The reason that some of the protons are likely to be missed.

Interpretation: The reason that some of the protons are likely to be missed is to be stated.

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.

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Answer 5

Chapter 13.11B, Problem 13.21P

(a)

Interpretation Introduction

To determine: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets.

Interpretation: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets is to be stated.

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.

(b)

Interpretation Introduction

To determine: The reason that some of the protons are likely to be missed.

Interpretation: The reason that some of the protons are likely to be missed is to be stated.

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.

Answer 6

Chapter 13.11B, Problem 13.21P

(a)

Interpretation Introduction

To determine: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets.

Interpretation: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets is to be stated.

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.

Answer 7

Chapter 13.11B, Problem 13.21P

(a)

Interpretation Introduction

To determine: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets.

Interpretation: The structure of the given NMR spectrum and an explanation as to why the peaks around $δ 1.65$ and $δ 3.75$ show complex splitting even when these are not clean multiplets is to be stated.

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.

Answer 8

(b)

Interpretation Introduction

To determine: The reason that some of the protons are likely to be missed.

Interpretation: The reason that some of the protons are likely to be missed is to be stated.

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.

Answer 9

(b)

Interpretation Introduction

To determine: The reason that some of the protons are likely to be missed.

Interpretation: The reason that some of the protons are likely to be missed is to be stated.

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.

Answer 10

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Answer 11

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Answer 12

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Answer 13

Ch. 13.5A - In a 300-MHz spectrometer, the protons in...Ch. 13.5B - Prob. 13.2P Ch. 13.6 - Determine the number of different kinds of protons...Ch. 13.6 - Prob. 13.4P Ch. 13.7 - Draw the integral trace expected for the NMR...Ch. 13.7 - Prob. 13.6P Ch. 13.8C - Draw the NMR spectra you would expect for the...Ch. 13.8D - Draw the NMR spectra you expect for the following...Ch. 13.8D - a. Assign protons to the peaks in the NMR spectrum...Ch. 13.8D - Prob. 13.10P

Solution Summary: The author explains NMR spectroscopy as a technique used to determine the carbon-hydrogen bonding of an organic compound.

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