% Transmittance 100 0 4000 doublet, 1H 7 200 6 3000 doublet, 1H. (e) 180 6 5 160 2000 1500 Wavenumber (cm-1) triplet, 2H (b) 140 (z) 4 PPM 120 PPM 3 100 singlet, 6H du b (a) 1000 triplet, 2H, (c) 80 2 60 alduob 40 500 Hi atsuob (o (f) 20 0

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The chemical formula is C8H12O. What is it’s structure and degrees of unsaturation? What important functional groups are in the spectra, and what peaks correspond with which hydrogens and carbons in the structure predicted.
### Infrared (IR) Spectrum

**Graph Description:**

- **X-axis (Wavenumber):** This graph plots wavenumber, ranging from 4000 cm⁻¹ to 500 cm⁻¹. 
- **Y-axis (% Transmittance):** The percentage of light transmitted through the sample, with the scale from 0% to 100%.
- **Features:**
  - Multiple peaks and troughs indicating different functional groups in the compound. 
  - Strong absorption bands are observable, typical for characterizing chemical bonds and structures.

### Proton Nuclear Magnetic Resonance (¹H NMR) Spectrum

**Graph Description:**

- **X-axis (PPM):** Chemical shift in parts per million (PPM).
- **Peaks and Assignments:**
  - **a:** Singlet, 6H observed near 1 PPM.
  - **b:** Triplet, 2H around 3 PPM.
  - **c:** Triplet, 2H close to 1.5 PPM.
  - **d:** Doublet, 1H appearing at 6.5 PPM.
  - **e:** Doublet, 1H near 5.5 PPM.

### Carbon-13 Nuclear Magnetic Resonance (¹³C NMR) Spectrum

**Graph Description:**

- **X-axis (PPM):** Chemical shift in PPM ranging from 0 to 220.
- **Peaks and Assignments:**
  - **x, y, z:** Peaks at 180, 160, and 130 PPM, respectively, showing various carbon environments.
  - **a:** Peak labeled around 30 PPM.
  - **b, c, f:** Peaks appearing between 15 and 25 PPM.

These spectra are invaluable for structural elucidation, offering insights into the chemical environment and connectivity of atoms within the compound.
Transcribed Image Text:### Infrared (IR) Spectrum **Graph Description:** - **X-axis (Wavenumber):** This graph plots wavenumber, ranging from 4000 cm⁻¹ to 500 cm⁻¹. - **Y-axis (% Transmittance):** The percentage of light transmitted through the sample, with the scale from 0% to 100%. - **Features:** - Multiple peaks and troughs indicating different functional groups in the compound. - Strong absorption bands are observable, typical for characterizing chemical bonds and structures. ### Proton Nuclear Magnetic Resonance (¹H NMR) Spectrum **Graph Description:** - **X-axis (PPM):** Chemical shift in parts per million (PPM). - **Peaks and Assignments:** - **a:** Singlet, 6H observed near 1 PPM. - **b:** Triplet, 2H around 3 PPM. - **c:** Triplet, 2H close to 1.5 PPM. - **d:** Doublet, 1H appearing at 6.5 PPM. - **e:** Doublet, 1H near 5.5 PPM. ### Carbon-13 Nuclear Magnetic Resonance (¹³C NMR) Spectrum **Graph Description:** - **X-axis (PPM):** Chemical shift in PPM ranging from 0 to 220. - **Peaks and Assignments:** - **x, y, z:** Peaks at 180, 160, and 130 PPM, respectively, showing various carbon environments. - **a:** Peak labeled around 30 PPM. - **b, c, f:** Peaks appearing between 15 and 25 PPM. These spectra are invaluable for structural elucidation, offering insights into the chemical environment and connectivity of atoms within the compound.
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