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Chapter 14 Solutions
ORGANIC CHEMISTRY
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- A ¹H NMR spectrum is shown for a molecule with the molecular formula of C10H12O4. Draw the structure that best fits this data. 1H 11 10 2H 2H U 7 1H 1H ΤΗ 1Η ppm Qarrow_forwardPls explain tooarrow_forwardFor each organic compound in the table below, enter the locant of the highlighted side chain. CH3 CH,— CH,— CH— CH, CH3 1 compound CH₂ | CH,—C− CH,—CH — CH CH3 モー CH3 CH,—CH— CH,—C— CH | CH₂ CH3 CH3 | CH3 locant of highlighted side chain 0 X Sarrow_forward
- Propose a structural formula for the analgesic phenacetin, molecular formula C10H13NO2, based on its 1H-NMR spectrum.arrow_forwardCompound 1 has molecular formula C7H16. It shows three signals in the 1H-NMR spectrum, one at 0.85 ppm, one at 1.02 ppm, and one at 1.62 ppm. The relative integrals of these three signals are 6, 1, and 1, respectively. Compound 2 has molecular formula C7H14. It shows three signals in the 1H-NMR spectrum, one at 0.98 ppm, one at 1.36 ppm, and one at 1.55 ppm. The relative integrals of these three signals are 3, 2, and 2, respectively. Propose structures for compounds 1 and 2, explaining how you reach your conclusion.arrow_forwardDraw the structure of the compound from the NMR spectra. Mark the peaks that help you find the compound.arrow_forward
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