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A: The structure of the unknown compound of molecular formula C8H8O3 is shown below:
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Suggest structures given the 1H NMR spectra and formulas for each of the compounds below.
C9H10O
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- A ¹H NMR spectrum is shown for a molecule with the molecular formula of C9H10O2. Draw the structure that best fits this data. 1H 11 10 9 8 SH 7 4 214 21 1 pom Q11 10 9 8 7 9 +6 5 -3 2 1 ppmCompound 2 has molecular formula C6H12. It shows three signals in the 1H-NMR spectrum, one at 0.96 ppm, one at 2.03 ppm, and one at 5.33 ppm. The relative integrals of these three signals are 3, 2, and 1, respectively. Provide structure for compound 2, explain how you reached your conclusion.
- 08) The NMR spectra of the two isomeric compounds with formula C3H5ClO2 are shown in letters a and b. Low-field protons appearing in the NMR spectrum around 12.1 and 11.5 ppm, respectively, are shown highlighted. Draw the structures of the isomers.The H1H1 NMR spectrum shown corresponds to an unknown compound with the molecular formula C6H10C6H10. There are no strong IR bands between 2100 and 2300 or 3250 and 3350 cm−1. Deduce and draw the structure of the molecule that corresponds to the spectrum.Identify the compound with molecular formula C8H10O that gives the IR and 1H NMR spectra shown here.
- Solve the structure of this compound by looking at the 1H, 13C NMR data provided. You must fill all of the parts to this question in the given spaces. Molecular formula: C6H14N2O2Propose a structural formula for the analgesic phenacetin, molecular formula C10H13NO2, based on its 1H-NMR spectrum.identify the compound with molecular formula C2H6O that gives this 1H NMR spectrum.