Using the 1H NMR and 13C NMR Data avalible at the end of the question, deduce...
C9H12 13C NMR 7 peaks 1H NMR δ 1.13 (triplet, 3H); δ 1.71 (multiplet, 2H); δ 2.64 (triplet, 2H); δ 7.34 (multiplet, 5H) Degree of Unsaturation _______ Draw the structure of your compound and indicate the ppm of each of the H’s. 2. C5H10O2 13C NMR 5 peaks 1H NMR δ 0.93 (triplet, 3H); δ 1.70 (multiplet, 2H); δ 2.25 (triplet, 2H); δ 3.59 (singlet, 3H) Degree of Unsaturation _______ Draw the structure of your compound and indicate the ppm...
1. Provide the 1H and 13C NMR data for 4-ethyl-1-cyclohexanecarboxaldehye Report the 1H NMR data in the sequence: chemical shift, integration, multiplicity (e.g. 1.0, 3H, triplet). Be sure to clearly label which proton and carbon you are reporting. 2. Provide the 1H and 13C NMR data for ethylene glycol. Report the 1H NMR data in the sequence: chemical shift, integration, multiplicity (e.g. d 1.0, 3H, triplet). Be sure to clearly label which proton and carbon you are reporting.
Provide the 1H and 13C NMR data for thiophenol. Note the chemical shift, multiplicity, and integration for each (e.g. d 1.0, 3H, triplet). Clearly identify which proton is being reported and which carbon is being reported. Provide the 1H and 13C NMR data for the product generated in Question #1. Note the chemical shift, multiplicity, and integration for each (e.g. d 1.0, 3H, triplet). Clearly identify which proton is being reported and which carbon is being reported.
Propose a reasonable structure based on the molecular formula,
the 1H NMR, and the proton–decoupled 13C NMR data below. The
unknown compound has a molecular formula of C7H16O and * = CH2 by
DEPT.
Propose a reasonable structure based on the molecular formula, the 'H NMR, and the proton-decoupled 13C NMR data below. The unknown compound has a molecular formula of C7H160 and * = CH2 by DEPT. 'H NMR 3H 8H 13C NMR 2H (CH3)4 Si 26 VIH them...
Deduce the final structure consistent to the 1H-NMR data. C4H8O2 1.2 ppm (triplet, 3H), 2.3 ppm (quartet, 2H), 3.6 ppm (singlet, 3H)
Deduce the final structure consistent to the 1H-NMR data. C5H9BrO2 1.2 ppm (triplet, 3H), 2.9 ppm (triplet, 2H), 3.5 ppm (triplet, 2H), 4.0 ppm (quartet, 2H)
Deduce the final structure consistent to the 1H-NMR data. C10H12O2 1.2 ppm (triplet, 3H), 3.5 ppm (singlet, 2H), 4.1 ppm (quartet, 2H), 7.1 ppm (singlet, 5H)
Deduce the final structure consistent to the 1H-NMR data. C9H10O2 2.1 ppm (singlet, 3H), 4.3 ppm (singlet, 2H), 7.3 ppm (singlet, 5H)
Deduce the final structure consistent to the 1H-NMR data. C10H12O2 2.0ppm(singlet, 3H), 2.9 ppm (triplet, 2H), 4.3 ppm (triplet, 2H)7.3 ppm (singlet, 5H)
Deduce the identity of the following compound from the spectral data given. C_4H_8O_2:^1H NMR, delta 1.23 (3H, triplet), 2.00 (3H, singlet), 4.02 (2H, quartet) (ppm); IR, 2980, 1740 cm^-1.