The structure of compound of given molecular formula C 7 H 12 O 2 to be predicted using 13 CNMR spectra. Concept introduction: The 13 CNMR spectrum gives information on the different electronic environments of carbon. As like 1 HNMR, the number of signals generated in 13 CNMR are predicted by performing symmetry operations (rotation or reflection symmetry). Only chemical shift values are reported in the spectrum but not the multiplicity and integration values because the coupling between two neighboring 13 C- 13 C nuclei are weakly involved due to the low abundance of 13 C isotopes of carbon atom. To Identify: The structure of given molecular formula C 7 H 12 O 2 . Broadband-decoupled 13 CNMR spectrum: The spectra provide information regarding the total number of carbon environments. DEPT (Distortionless enhancement by polarization transfer): a) DEPT-90: The spectrum exhibits signal only from CH group and no signals from CH 3 , CH 2 , CH and quaternary carbon (carbon with no protons). b) DEPT-135: The spectrum exhibits CH 3 groups and CH groups as positive signals (pointing up); CH 2 groups appear as negative signals (pointing down) and quaternary carbon does not appear. The signals appear in each type of spectrum:

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Answer 1

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Chapter 13.12, Problem 21P

Interpretation Introduction

Interpretation:

The structure of compound of given molecular formula C₇H₁₂O₂ to be predicted using ¹³CNMR spectra.

Concept introduction:

The ¹³CNMR spectrum gives information on the different electronic environments of carbon. As like ¹HNMR, the number of signals generated in ¹³CNMR are predicted by performing symmetry operations (rotation or reflection symmetry). Only chemical shift values are reported in the spectrum but not the multiplicity and integration values because the coupling between two neighboring ¹³C-¹³ C nuclei are weakly involved due to the low abundance of ¹³C isotopes of carbon atom.

To Identify:

The structure of given molecular formula C₇H₁₂O₂.

Broadband-decoupled ¹³CNMR spectrum:

The spectra provide information regarding the total number of carbon environments.

DEPT (Distortionless enhancement by polarization transfer):

a) DEPT-90: The spectrum exhibits signal only from CH group and no signals from CH₃, CH₂, CH and quaternary carbon (carbon with no protons).

b) DEPT-135: The spectrum exhibits CH₃ groups and CH groups as positive signals (pointing up); CH₂ groups appear as negative signals (pointing down) and quaternary carbon does not appear.

The signals appear in each type of spectrum:

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Answer 2

Question

Chapter 13.12, Problem 21P

Interpretation Introduction

Interpretation:

The structure of compound of given molecular formula C₇H₁₂O₂ to be predicted using ¹³CNMR spectra.

Concept introduction:

The ¹³CNMR spectrum gives information on the different electronic environments of carbon. As like ¹HNMR, the number of signals generated in ¹³CNMR are predicted by performing symmetry operations (rotation or reflection symmetry). Only chemical shift values are reported in the spectrum but not the multiplicity and integration values because the coupling between two neighboring ¹³C-¹³ C nuclei are weakly involved due to the low abundance of ¹³C isotopes of carbon atom.

To Identify:

The structure of given molecular formula C₇H₁₂O₂.

Broadband-decoupled ¹³CNMR spectrum:

The spectra provide information regarding the total number of carbon environments.

DEPT (Distortionless enhancement by polarization transfer):

a) DEPT-90: The spectrum exhibits signal only from CH group and no signals from CH₃, CH₂, CH and quaternary carbon (carbon with no protons).

b) DEPT-135: The spectrum exhibits CH₃ groups and CH groups as positive signals (pointing up); CH₂ groups appear as negative signals (pointing down) and quaternary carbon does not appear.

The signals appear in each type of spectrum:

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Answer 3

Question

Chapter 13.12, Problem 21P

Interpretation Introduction

Interpretation:

The structure of compound of given molecular formula C₇H₁₂O₂ to be predicted using ¹³CNMR spectra.

Concept introduction:

The ¹³CNMR spectrum gives information on the different electronic environments of carbon. As like ¹HNMR, the number of signals generated in ¹³CNMR are predicted by performing symmetry operations (rotation or reflection symmetry). Only chemical shift values are reported in the spectrum but not the multiplicity and integration values because the coupling between two neighboring ¹³C-¹³ C nuclei are weakly involved due to the low abundance of ¹³C isotopes of carbon atom.

To Identify:

The structure of given molecular formula C₇H₁₂O₂.

Broadband-decoupled ¹³CNMR spectrum:

The spectra provide information regarding the total number of carbon environments.

DEPT (Distortionless enhancement by polarization transfer):

a) DEPT-90: The spectrum exhibits signal only from CH group and no signals from CH₃, CH₂, CH and quaternary carbon (carbon with no protons).

b) DEPT-135: The spectrum exhibits CH₃ groups and CH groups as positive signals (pointing up); CH₂ groups appear as negative signals (pointing down) and quaternary carbon does not appear.

The signals appear in each type of spectrum:

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Answer 4

Question

Chapter 13.12, Problem 21P

Interpretation Introduction

Interpretation:

The structure of compound of given molecular formula C₇H₁₂O₂ to be predicted using ¹³CNMR spectra.

Concept introduction:

The ¹³CNMR spectrum gives information on the different electronic environments of carbon. As like ¹HNMR, the number of signals generated in ¹³CNMR are predicted by performing symmetry operations (rotation or reflection symmetry). Only chemical shift values are reported in the spectrum but not the multiplicity and integration values because the coupling between two neighboring ¹³C-¹³ C nuclei are weakly involved due to the low abundance of ¹³C isotopes of carbon atom.

To Identify:

The structure of given molecular formula C₇H₁₂O₂.

Broadband-decoupled ¹³CNMR spectrum:

The spectra provide information regarding the total number of carbon environments.

DEPT (Distortionless enhancement by polarization transfer):

a) DEPT-90: The spectrum exhibits signal only from CH group and no signals from CH₃, CH₂, CH and quaternary carbon (carbon with no protons).

b) DEPT-135: The spectrum exhibits CH₃ groups and CH groups as positive signals (pointing up); CH₂ groups appear as negative signals (pointing down) and quaternary carbon does not appear.

The signals appear in each type of spectrum:

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Answer 5

Chapter 13.12, Problem 21P

Interpretation Introduction

Interpretation:

The structure of compound of given molecular formula C₇H₁₂O₂ to be predicted using ¹³CNMR spectra.

Concept introduction:

The ¹³CNMR spectrum gives information on the different electronic environments of carbon. As like ¹HNMR, the number of signals generated in ¹³CNMR are predicted by performing symmetry operations (rotation or reflection symmetry). Only chemical shift values are reported in the spectrum but not the multiplicity and integration values because the coupling between two neighboring ¹³C-¹³ C nuclei are weakly involved due to the low abundance of ¹³C isotopes of carbon atom.

To Identify:

The structure of given molecular formula C₇H₁₂O₂.

Broadband-decoupled ¹³CNMR spectrum:

The spectra provide information regarding the total number of carbon environments.

DEPT (Distortionless enhancement by polarization transfer):

a) DEPT-90: The spectrum exhibits signal only from CH group and no signals from CH₃, CH₂, CH and quaternary carbon (carbon with no protons).

b) DEPT-135: The spectrum exhibits CH₃ groups and CH groups as positive signals (pointing up); CH₂ groups appear as negative signals (pointing down) and quaternary carbon does not appear.

The signals appear in each type of spectrum:

Answer 6

Chapter 13.12, Problem 21P

Interpretation Introduction

Interpretation:

The structure of compound of given molecular formula C₇H₁₂O₂ to be predicted using ¹³CNMR spectra.

Concept introduction:

The ¹³CNMR spectrum gives information on the different electronic environments of carbon. As like ¹HNMR, the number of signals generated in ¹³CNMR are predicted by performing symmetry operations (rotation or reflection symmetry). Only chemical shift values are reported in the spectrum but not the multiplicity and integration values because the coupling between two neighboring ¹³C-¹³ C nuclei are weakly involved due to the low abundance of ¹³C isotopes of carbon atom.

To Identify:

The structure of given molecular formula C₇H₁₂O₂.

Broadband-decoupled ¹³CNMR spectrum:

The spectra provide information regarding the total number of carbon environments.

DEPT (Distortionless enhancement by polarization transfer):

a) DEPT-90: The spectrum exhibits signal only from CH group and no signals from CH₃, CH₂, CH and quaternary carbon (carbon with no protons).

b) DEPT-135: The spectrum exhibits CH₃ groups and CH groups as positive signals (pointing up); CH₂ groups appear as negative signals (pointing down) and quaternary carbon does not appear.

The signals appear in each type of spectrum:

Answer 7

Chapter 13.12, Problem 21P

Interpretation Introduction

Interpretation:

The structure of compound of given molecular formula C₇H₁₂O₂ to be predicted using ¹³CNMR spectra.

Concept introduction:

The ¹³CNMR spectrum gives information on the different electronic environments of carbon. As like ¹HNMR, the number of signals generated in ¹³CNMR are predicted by performing symmetry operations (rotation or reflection symmetry). Only chemical shift values are reported in the spectrum but not the multiplicity and integration values because the coupling between two neighboring ¹³C-¹³ C nuclei are weakly involved due to the low abundance of ¹³C isotopes of carbon atom.

To Identify:

The structure of given molecular formula C₇H₁₂O₂.

Broadband-decoupled ¹³CNMR spectrum:

The spectra provide information regarding the total number of carbon environments.

DEPT (Distortionless enhancement by polarization transfer):

a) DEPT-90: The spectrum exhibits signal only from CH group and no signals from CH₃, CH₂, CH and quaternary carbon (carbon with no protons).

b) DEPT-135: The spectrum exhibits CH₃ groups and CH groups as positive signals (pointing up); CH₂ groups appear as negative signals (pointing down) and quaternary carbon does not appear.

The signals appear in each type of spectrum:

Answer 8

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Answer 11

Ch. 13.1 - Prob. 1P Ch. 13.1 - Prob. 2P Ch. 13.2 - Prob. 3P Ch. 13.3 - The following 1H NMR peaks were recorded on a...Ch. 13.3 - When the 1Î— NMR spectrum of acetone, CH3COCH3, is...Ch. 13.4 - Each of the following compounds has a single 1H...Ch. 13.4 - Identify the different types of protons in the...Ch. 13.5 - How many peaks would you expect in the 1H NMR...Ch. 13.6 - Predict the splitting patterns you would expect...Ch. 13.6 - Draw structures for compounds that meet the...

Solution Summary: The author explains that the 13 CNMR spectrum gives information on the different electronic environments of carbon.

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