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In the "H NMR spectrum recorded at 293 K, an organic compound (C,H,NO), exhibited signals at 6 7.8 (1H, 5), 2.8 (3H, s), 2.6 (3H, s). the compound is
[NET Dec 2012]?
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In the "H NMR spectrum recorded at 293 K, an organic compound (C,H,NO)...
- **Identification of the Compound based on H NMR data**
- **Chemical Shifts and Integration Values:**
The H NMR spectrum shows signals at 7.8 ppm (singlet, 1H), 2.8 ppm (triplet, 3H), and 2.6 ppm (triplet, 3H).
- **Interpreting the Data:**
The signal at 7.8 ppm corresponds to a hydrogen atom attached to a carbon atom that is most likely electron-deficient, such as a carbonyl group. The integration value of 5 indicates the presence of 5 hydrogens in this environment.
The signals at 2.8 ppm and 2.6 ppm are likely to be methyl groups due to their chemical shift values and integration values of 3 each.
- **Structure Determination:**
Based on the data provided, the compound is most likely acetophenone (C8H8O). This compound contains a carbonyl group (C=O) which resonates at around 7.8 ppm in the H NMR spectrum. The two methyl groups in the compound give rise to signals at 2.8 ppm and 2.6 ppm.
- **Conclusion:**
Therefore, the organic compound (C,H,NO) analyzed in the H NMR spectrum is likely to be acetophenone based on the chemical shifts and integration values observed in the spectrum.
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In the "H NMR spectrum recorded at 293 K, an organic compound (C,H,NO), exhibited signals at 6 7.8 (1H, 5), 2.8 (3H, s), 2.6 (3H, s). the compound is[NET Dec 2012]?
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