Please ### 'H NMR Spectrum AnalysisThe table below analyzes the ^1H NMR spectrum of an unknown compound G, with a molecular formula of C7H14O. The data presents chemical shifts, integration, multiplicity, and the number of neighboring hydrogen atoms, which help identify the partial structure.| δ (ppm) | Integration | Multiplicity | # of Neighboring H | Partial Structure ||---------|-------------|--------------|--------------------|-------------------|| 2.08 | 2 | Doublet | 1 | || 9.58 | 9 | Singlet | 0 | || 3.00 | 3 | Triplet | 2 | |### ^13C NMR Spectrum AnalysisThe table below should be completed using the ^13C NMR spectrum for the same unknown compound G. Each signal is assigned to a partial structure.| Partial Structure | Partial Structure ||-------------------|-------------------|| a | d || b | e |### Structural Assignment- **Hydrogen Assignments:** Assign the hydrogen signals (A-C) to the appropriate protons in the molecule.- **Carbon Assignments:** Assign the carbon signals (a-e) to the corresponding carbon atoms in the molecule's structure.### NMR Spectra Explanation#### ^1H NMR Spectrum for C7H14O:- The spectrum shows three distinct peaks: - **Peak A**: At 2.08 ppm, with an integration of 2 generating a doublet, indicating a hydrogen atom next to one other hydrogen. - **Peak B**: At 9.58 ppm, with an integration of 9 and a singlet, suggesting the presence of a isolated hydrogen environment without neighboring hydrogens. - **Peak C**: At 3.00 ppm, with an integration of 3 producing a triplet, indicative of hydrogen atoms adjacent to two other hydrogens.#### ^13C NMR Spectrum for C7H14O:- The spectrum includes several peaks labeled a to e: - **Peak a** begins near 220 ppm. - Additional peaks labeled b, c,

Answered: 3. Complete the following table based…

3. Complete the following table based on the 'H NMR spectrum of unknown compound G whose molecular formula is C,H140. 2x2+2=14=7I # of 8 (ppm) Integration Multiplicity Partial structure neighboring H

Chemistry

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ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Mass Spectrometry

This process is an instrumental method in which a sample is changed to fast moving positive ions by electron bombardment. The charged particles vary due to their different mass to charge ratio and are estimated with the help of this difference. It is also called mass spectroscopy.

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Please

### 'H NMR Spectrum Analysis

The table below analyzes the ^1H NMR spectrum of an unknown compound G, with a molecular formula of C<sub>7</sub>H<sub>14</sub>O. The data presents chemical shifts, integration, multiplicity, and the number of neighboring hydrogen atoms, which help identify the partial structure.

| δ (ppm) | Integration | Multiplicity | # of Neighboring H | Partial Structure |
|---------|-------------|--------------|--------------------|-------------------|
| 2.08 | 2 | Doublet | 1 | |
| 9.58 | 9 | Singlet | 0 | |
| 3.00 | 3 | Triplet | 2 | |

### ^13C NMR Spectrum Analysis

The table below should be completed using the ^13C NMR spectrum for the same unknown compound G. Each signal is assigned to a partial structure.

| Partial Structure | Partial Structure |
|-------------------|-------------------|
| a | d |
| b | e |

### Structural Assignment

- **Hydrogen Assignments:** Assign the hydrogen signals (A-C) to the appropriate protons in the molecule.
- **Carbon Assignments:** Assign the carbon signals (a-e) to the corresponding carbon atoms in the molecule's structure.

### NMR Spectra Explanation

#### ^1H NMR Spectrum for C<sub>7</sub>H<sub>14</sub>O:

- The spectrum shows three distinct peaks:
- **Peak A**: At 2.08 ppm, with an integration of 2 generating a doublet, indicating a hydrogen atom next to one other hydrogen.
- **Peak B**: At 9.58 ppm, with an integration of 9 and a singlet, suggesting the presence of a isolated hydrogen environment without neighboring hydrogens.
- **Peak C**: At 3.00 ppm, with an integration of 3 producing a triplet, indicative of hydrogen atoms adjacent to two other hydrogens.

#### ^13C NMR Spectrum for C<sub>7</sub>H<sub>14</sub>O:

- The spectrum includes several peaks labeled a to e:
- **Peak a** begins near 220 ppm.
- Additional peaks labeled b, c,

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