An unknown compound has the molecular formula C7H14O, and its 1H NMR and 13C NMR spectra are shown here. Determine the structure of the unknown compound and draw it below. Note that there are no peaks above 3 ppm in the 1H NMR, and the numbers present on the 1H NMR are the integration values for each set of peaks. (Also note that the protons responsible for causing the splitting pattern seen for the "9 peak" multiplet have similar coupling constants.) Andrés M. Castillo, Luc Patiny and Julien Wist. Fast and Accurate Algorithm for the Simulation of NMR spectra of Large Spin Systems. Journal of Magnetic Resonance 2011. 1H Spectrum 13C Spectrum
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This suggests a degree of unsaturation of 1, indicating the presence of a ring or a double bond. Show more…
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