IR spectrum of maleic anhydride 100 80 - 60 40 - 20 - 4000 3600 3200 2800 2400 2000 1800 1600 1400 1200 1000 800 600 Wavenumber (cm-1) Transmittance (%)

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In the functional group region of the IR spectrum, specify the absorptions
associated with the carbon-carbon and carbon-oxygen double bonds.

**IR Spectrum of Maleic Anhydride**

The image displays an infrared (IR) spectrum graph for maleic anhydride. The spectrum is illustrated as a line graph with the following components:

- **X-Axis (Wavenumber)**: This is labeled as "Wavenumber (cm⁻¹)" and spans from 4000 to 600 cm⁻¹.
- **Y-Axis (Transmittance)**: This is labeled as "Transmittance (%)" and ranges from 0% to 100%.

**Key Features of the Graph:**

- The spectrum shows various peaks at different wavenumbers, indicating the absorption frequencies of maleic anhydride.
- Main peaks can be observed at wavenumbers around 1800 cm⁻¹, 1700 cm⁻¹, and multiple sharp peaks between 1000 cm⁻¹ and 600 cm⁻¹, which are characteristic of functional groups in the compound.
- The structural formula of maleic anhydride is depicted centrally on the graph, indicating its chemical structure and making a reference to the molecular bonds responsible for specific absorption bands.

This spectrum is useful for identifying the presence of maleic anhydride by comparing the observed absorption bands with known characteristic frequencies of different functional groups.
Transcribed Image Text:**IR Spectrum of Maleic Anhydride** The image displays an infrared (IR) spectrum graph for maleic anhydride. The spectrum is illustrated as a line graph with the following components: - **X-Axis (Wavenumber)**: This is labeled as "Wavenumber (cm⁻¹)" and spans from 4000 to 600 cm⁻¹. - **Y-Axis (Transmittance)**: This is labeled as "Transmittance (%)" and ranges from 0% to 100%. **Key Features of the Graph:** - The spectrum shows various peaks at different wavenumbers, indicating the absorption frequencies of maleic anhydride. - Main peaks can be observed at wavenumbers around 1800 cm⁻¹, 1700 cm⁻¹, and multiple sharp peaks between 1000 cm⁻¹ and 600 cm⁻¹, which are characteristic of functional groups in the compound. - The structural formula of maleic anhydride is depicted centrally on the graph, indicating its chemical structure and making a reference to the molecular bonds responsible for specific absorption bands. This spectrum is useful for identifying the presence of maleic anhydride by comparing the observed absorption bands with known characteristic frequencies of different functional groups.
**Experiment: Diels-Alder (D-A)**

**Title:** Diels-Alder Reaction (Otto and Kurt). Cycloaddition of Maleic Anhydride with Anthracene

**Reference:** Hill, R. K.; Barbaro, J. *Experiments in Organic Chemistry* (2000, 2nd Ed) pp. E7-1-3.

**Purpose:** Synthesize 9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboxylic anhydride

**Reaction Diagram:**

- **Reactants:** 
  - Anthracene
  - Maleic Anhydride
- **Reaction Conditions:** Reflux
- **Product:** The diagram shows the chemical structure of the resulting cycloadduct.

**Reagent Table:**

| Reagent (Source)         | Mwt   | mp °C | bp °C | (Fp) | mmol | Mass (%)  | Density | Volume |
|--------------------------|-------|-------|-------|------|------|-----------|---------|--------|
| Anthracene (Acros)       | 178.23| 216-8 | -     | (121)| 10.1 | 1.84 g (98%) | -       | -      |
| Maleic Anhydride (Acros) | 98.06 | 54-56 | 200   | (103)| 10.1 | 1.00 g (99%) | -       | -      |
| Toluene (anhyd.) (Pharmaco)| -   | -     | 111   | -    | -    | -         | 0.87    | 43 mL  |
| Cycloadduct              | 276.29| 261-2 | -     | -    | 10.1 | 2.79 g    | -       | -      |

- **Key:** 
  - Mwt: Molecular weight
  - mp: Melting point
  - bp: Boiling point
  - Fp: Flash point

**Revision Date:** 03/09/2010ssh

This experiment demonstrates a Diels-Alder reaction between anthracene and maleic anhydride, resulting in the formation of a cycloadduct. The details such as molecular weights, melting and boiling points, and reactant ratios provide necessary
Transcribed Image Text:**Experiment: Diels-Alder (D-A)** **Title:** Diels-Alder Reaction (Otto and Kurt). Cycloaddition of Maleic Anhydride with Anthracene **Reference:** Hill, R. K.; Barbaro, J. *Experiments in Organic Chemistry* (2000, 2nd Ed) pp. E7-1-3. **Purpose:** Synthesize 9,10-dihydro-9,10-ethanoanthracene-11,12-dicarboxylic anhydride **Reaction Diagram:** - **Reactants:** - Anthracene - Maleic Anhydride - **Reaction Conditions:** Reflux - **Product:** The diagram shows the chemical structure of the resulting cycloadduct. **Reagent Table:** | Reagent (Source) | Mwt | mp °C | bp °C | (Fp) | mmol | Mass (%) | Density | Volume | |--------------------------|-------|-------|-------|------|------|-----------|---------|--------| | Anthracene (Acros) | 178.23| 216-8 | - | (121)| 10.1 | 1.84 g (98%) | - | - | | Maleic Anhydride (Acros) | 98.06 | 54-56 | 200 | (103)| 10.1 | 1.00 g (99%) | - | - | | Toluene (anhyd.) (Pharmaco)| - | - | 111 | - | - | - | 0.87 | 43 mL | | Cycloadduct | 276.29| 261-2 | - | - | 10.1 | 2.79 g | - | - | - **Key:** - Mwt: Molecular weight - mp: Melting point - bp: Boiling point - Fp: Flash point **Revision Date:** 03/09/2010ssh This experiment demonstrates a Diels-Alder reaction between anthracene and maleic anhydride, resulting in the formation of a cycloadduct. The details such as molecular weights, melting and boiling points, and reactant ratios provide necessary
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