![]() |
Infrared Spectroscopy, Example #3
Analysis: C7H8O
Help with Analysis
IR Spectrum
| Correlation Table | Common Absorbances | Interpret IR |
| Give Structure | Next Example | Return to IR Home |

From the molecular formula, the compound has "4 degrees of unsaturation" (four double bonds, carbonyls or rings). The large number suggests the possible presence of an aromatic ring (4 degrees of unsaturation).

| 3400-3200 cm-1: | strong peak indicating OH is present |
| 3100 cm-1: | weak peak suggesting possible unsaturated CH |
| 2900 cm-1: | weak peak indicating possible saturated CH |
| 2200 cm-1: | no unsymmetrical triple bonds |
| 1720 cm-1: | no carbonyl absorbance |
| 1450-1500 cm-1: | moderate absorbance bands consistent with aromatic carbon-carbon double bonds |
Click here for a review on Infrared Spectroscopy NMR.
Click here to view an IR correlation table.
