Draw the structure of the compound identified by the simulated H1 NMR and C13 NMR spectra. The molecular formula of the compound is C10H12O . (Blue numbers next to the lines in the H1 NMR spectra indicate the integration values.) The proton NMR spectrum has 6 resonances. There is a triplet at 9.8 ppm integrating to 1 proton. There are two sets of doublets, each integrating to two protons, at 7.2 ppm. There is a doublet at 3.8 ppm integrating to 2 protons. There is a quartet at 2.7 ppm integrating to 2 protons. There is a triplet at 1.2 ppm integrating to 3 protons. The carbon 13 NMR has 8 peaks, located at 15, 28, 51, 143 and 199 ppm. There are also 3 peaks between 125 and 130 ppm.
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Chemistry, 21.06.2019 21:00, david838843
Iwll give extra points to who gets this for ! what type of reaction is this? ?
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Chemistry, 22.06.2019 16:00, bbrogle5154
If 15 drops of ethanol from a medical dropper weight 0.60g, how many drops does it takes from a dropper to dispense 1.0ml of ethanol? the density of ethanol is 0.80g/ml
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Chemistry, 22.06.2019 16:50, briansalazar17
Answer asap need by wednesday morning calculate the ph of 0.16m ch3cooh which has ka = 1.74 x 10-5 mol dm-3 best answer will be brainliest
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Draw the structure of the compound identified by the simulated H1 NMR and C13 NMR spectra. The molec...
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