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- 10 3 9 8 (ppm) 8 2 7 6 5 8 (ppm) 4 1.00 1.50 3 2 1.50 1 0What is the 1H NMR data (chemical shift, integration, multiplicity (specify as singlet, doublet, triplet,etc.) of the following two compounds?Draw the H1 NMR spectra of ethylcyclopropane. Draw the chemical structure and predict the proton splitting and chemical shifts.
- An unknown compound has the formula C3H7NO2. Elucidate its structure by scrutinizing its 1H NMR spectra, shown. Specifically, label each different type of H atom in the final structure with its NMR chemical shift in ppm.Sketch the 1H NMR spectra of the following compounds.How could 1H NMR spectroscopy be used to distinguish betweencompounds X and Y?
- Draw the structure of the compound identified by the simulated 'H NMR and 13C NMR spectra. The molecular formula of the compound is C1,H120. (Blue numbers next to the lines in the 'H NMR spectra indicate the integration values.) Η NMR 1H 2H 2H 2H 2H 3H| 10 8 4 2 8 (ppm) 13C NMR 220 200 180 160 140 120 100 80 60 40 20 d (ppm)Part C Look at the NMR spectrum and list the structural characteristics you can determine from that spectrum. 200 180 160 140 120 100 80 60 40 20 13C NMR (CH, (CH, (CH) |(CH) CDCI (CH) (C) SOH SOH 7.18 708 6.18 6.08 CHCI, 10 8 (ppm) Part D Look at the set of spectra as a group and propose a structure the compound.give structure of this c-nmr spectrum
- Indicate two basic differences that exist between the spectra of 1H y 13C in NMR.Determine the structure from the FTIR and mass spectrum. The proton NMR has a singlet with an integration of 6 hydrogens at 2.6 ppm, a triplet with an integration of 1 hydrogen at 7.41 ppm, and a doublet with an integration of 3 hydrogens at 7.25 ppm.For the compounds below give the 1H NMR data (chemical shift, integration and multiplicity) I appreciate the help.