nterpret each of the following 1H NMR spectra. The integration for each peak is given above the peak. See the example for methyl ethyl ketone. All spectra were taken from http://riodb01.ibase.aist.go.jp/sdbs/cgi-bin/direct_frame_top.cgi.

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Interpret each of the following 1H NMR spectra. The integration for each peak is given above the peak. See the example for methyl ethyl ketone. All spectra were taken from http://riodb01.ibase.aist.go.jp/sdbs/cgi-bin/direct_frame_top.cgi.

**Nuclear Magnetic Resonance (NMR) Spectroscopy Analysis Example**

---

**Figure D**:

- **Chemical Structure:**
  The chemical structure at the top shows a molecule with a benzene ring substituted with a formyl group (-CHO) and a methyl group (-CH₃).

- **NMR Spectrum:**
  Below the chemical structure, there is an NMR spectrum with the x-axis labeled in parts per million (ppm) ranging from 11 to 0 ppm.
  - Peaks:
      - 1 Peak at around 3 ppm labeled as "3".
      - 2 Peaks between 7 and 8 ppm labeled as "2" and "3" respectively.
  - This spectrum corresponds to the hydrogen atoms in the chemical structure, showing their chemical environments and how they resonate in the magnetic field.

---

**Figure E**:

- **Chemical Structure:**
  The chemical structure at the top shows a molecule with a benzene ring substituted with two methyl groups (-CH₃) and an acetyl group (-COCH₃). 

- **NMR Spectrum:**
  Below the chemical structure, there is an NMR spectrum with the x-axis labeled in ppm ranging from 9 to 0 ppm.
    - Peaks:
        - 2 Peaks at around 2 ppm, each labeled as "2".
        - 2 Peaks between 6 and 8 ppm, each labeled as "2" or "3".
        - A peak slightly above 4 ppm labeled as "2".
        - Peaks close to 3 ppm labeled as "2" and "3".

---

**Explanation:**

Nuclear Magnetic Resonance (NMR) spectroscopy is a powerful analytical technique used to determine the structure of organic molecules. The chemical structure is deduced by analyzing the magnetic properties of certain atomic nuclei. The NMR spectrum shows the different environments of hydrogen atoms (protons) in the molecule and provides a fingerprint of the molecule's hydrogen atoms.

- The x-axis on the NMR spectrum represents the chemical shift in parts per million (ppm), which indicates the environment of the hydrogen atoms.
- The y-axis depicts the intensity of the signals, correlated with the number of hydrogen atoms in that chemical environment.
- Different hydrogen atoms in different environments within a molecule resonate at different frequencies, causing peaks at various points along the x-axis.

Understanding these spectra allows chemists to piece together the structure of the molecule, identify functional groups, and draw
Transcribed Image Text:**Nuclear Magnetic Resonance (NMR) Spectroscopy Analysis Example** --- **Figure D**: - **Chemical Structure:** The chemical structure at the top shows a molecule with a benzene ring substituted with a formyl group (-CHO) and a methyl group (-CH₃). - **NMR Spectrum:** Below the chemical structure, there is an NMR spectrum with the x-axis labeled in parts per million (ppm) ranging from 11 to 0 ppm. - Peaks: - 1 Peak at around 3 ppm labeled as "3". - 2 Peaks between 7 and 8 ppm labeled as "2" and "3" respectively. - This spectrum corresponds to the hydrogen atoms in the chemical structure, showing their chemical environments and how they resonate in the magnetic field. --- **Figure E**: - **Chemical Structure:** The chemical structure at the top shows a molecule with a benzene ring substituted with two methyl groups (-CH₃) and an acetyl group (-COCH₃). - **NMR Spectrum:** Below the chemical structure, there is an NMR spectrum with the x-axis labeled in ppm ranging from 9 to 0 ppm. - Peaks: - 2 Peaks at around 2 ppm, each labeled as "2". - 2 Peaks between 6 and 8 ppm, each labeled as "2" or "3". - A peak slightly above 4 ppm labeled as "2". - Peaks close to 3 ppm labeled as "2" and "3". --- **Explanation:** Nuclear Magnetic Resonance (NMR) spectroscopy is a powerful analytical technique used to determine the structure of organic molecules. The chemical structure is deduced by analyzing the magnetic properties of certain atomic nuclei. The NMR spectrum shows the different environments of hydrogen atoms (protons) in the molecule and provides a fingerprint of the molecule's hydrogen atoms. - The x-axis on the NMR spectrum represents the chemical shift in parts per million (ppm), which indicates the environment of the hydrogen atoms. - The y-axis depicts the intensity of the signals, correlated with the number of hydrogen atoms in that chemical environment. - Different hydrogen atoms in different environments within a molecule resonate at different frequencies, causing peaks at various points along the x-axis. Understanding these spectra allows chemists to piece together the structure of the molecule, identify functional groups, and draw
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