Calculation of HDI for each compound show work . Label and assign all the functional groups in the diagnostic region of the IR . Label and assign all protons in the NMR on your drawing ( clearly annotate each set of chemically non equivalent protons on your proposed structure and assign their signal on the 1H-NMR spectrum. .what lead to the proposed structure using the HDI,IR AND 1-H-NMR data provided.

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. Calculation of HDI for each compound show work . Label and assign all the functional groups in the diagnostic region of the IR . Label and assign all protons in the NMR on your drawing ( clearly annotate each set of chemically non equivalent protons on your proposed structure and assign their signal on the 1H-NMR spectrum. .what lead to the proposed structure using the HDI,IR AND 1-H-NMR data provided.
### Spectral Analysis of C\(_8\)H\(_{18}\)

#### Molecular Formula and Properties:

- **Molecular Formula:** C\(_8\)H\(_{18}\)
- **Molecular Weight (MW):** 114
- **Percentage of Carbon (\%C):** 84.1
- **Percentage of Hydrogen (\%H):** 15.9

#### Mass Spectrometry Data:

| m/z | Relative Abundance (%) |
|-----|------------------------|
| 27  | 9                      |
| 29  | 16                     |
| 39  | 9                      |
| 41  | 43                     |
| 43  | 24                     |
| 56  | 28                     |
| 57  | 100                    |
| 58  | 81                     |
| 99  | 2                      |

#### Infrared (IR) Spectrum:

The IR spectrum (upper graph) displays a range from 400 to 4000 cm\(^{-1}\). Significant absorption peaks include:

- Strong absorption near 2950 cm\(^{-1}\), indicating C-H stretching (alkanes).
- Additional peaks may represent various bending or stretching vibrations characteristic of hydrocarbons.

#### Proton NMR Spectrum:

The proton NMR spectrum (middle graph) displays chemical shifts in parts per million (PPM).

- Peaks at approximately 0.9 ppm (9H), 1.3 ppm (6H), and 1.5 ppm (2H) represent hydrogen environments typical of branched alkanes.
- Small peak at ~2.0 ppm (1H) could indicate a different hydrogen environment.

#### Carbon-13 NMR Spectrum:

The carbon-13 NMR spectrum (lower graph) shows shifts from 70 to 0 PPM.

- Peaks are observed at around 10, 20, 30, and 40 PPM, corresponding to different carbon environments within the molecule consistent with aliphatic hydrocarbons.

This spectral analysis helps in identifying and confirming the structure of C\(_8\)H\(_{18}\), commonly known as octane, by matching spectral features with known data.
Transcribed Image Text:### Spectral Analysis of C\(_8\)H\(_{18}\) #### Molecular Formula and Properties: - **Molecular Formula:** C\(_8\)H\(_{18}\) - **Molecular Weight (MW):** 114 - **Percentage of Carbon (\%C):** 84.1 - **Percentage of Hydrogen (\%H):** 15.9 #### Mass Spectrometry Data: | m/z | Relative Abundance (%) | |-----|------------------------| | 27 | 9 | | 29 | 16 | | 39 | 9 | | 41 | 43 | | 43 | 24 | | 56 | 28 | | 57 | 100 | | 58 | 81 | | 99 | 2 | #### Infrared (IR) Spectrum: The IR spectrum (upper graph) displays a range from 400 to 4000 cm\(^{-1}\). Significant absorption peaks include: - Strong absorption near 2950 cm\(^{-1}\), indicating C-H stretching (alkanes). - Additional peaks may represent various bending or stretching vibrations characteristic of hydrocarbons. #### Proton NMR Spectrum: The proton NMR spectrum (middle graph) displays chemical shifts in parts per million (PPM). - Peaks at approximately 0.9 ppm (9H), 1.3 ppm (6H), and 1.5 ppm (2H) represent hydrogen environments typical of branched alkanes. - Small peak at ~2.0 ppm (1H) could indicate a different hydrogen environment. #### Carbon-13 NMR Spectrum: The carbon-13 NMR spectrum (lower graph) shows shifts from 70 to 0 PPM. - Peaks are observed at around 10, 20, 30, and 40 PPM, corresponding to different carbon environments within the molecule consistent with aliphatic hydrocarbons. This spectral analysis helps in identifying and confirming the structure of C\(_8\)H\(_{18}\), commonly known as octane, by matching spectral features with known data.
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