Please show calculations for the corresponding number of
hydrogens for each peak cluster on the 1H NMR
spectrum.
Label all peaks in the 1H-NMR with the peak
closest to 0 with the letter A and continue labeling B,C, D going
from right to left. Additionally, label all the peaks in the
13C-NMR spectra with the peaks closest to 0 with the number 1 and
continue with 2, 3, 4, etc. from right to left.
Please help confirm that the molecular structure
corresponds with both NMR data. If it does not correspond, please
draw a molecule that is consistent with both spectra.
Assign each hydrogen in the structure to its
corresponding peak in the spectrum (a, b, c, etc.).
Assign each carbon in your structure to its
corresponding peak in the spectrum (1, 2, 3 etc.).
1.8 1.9 68.25 t LT C3H80 H-NMR 1.6 51 PT Degrees of unsaturation: 0 42.21 m 41.52 t 13 o 42.21 1.1 OT 60 2 19.41, broad s 0,7 모 2 CH2 HO 19:41 0.5 04 CH2 2 CH3 3 0.1 12,0 TL 10.0 8.0 & 5.0 4.0 3.0 20 -1.0 -20 3.5521 3.5406 1.5544 1.5383 1.5246 0.9117 PESKO TESSO 0.5648
С3Н8O C-NMR 3 unique carbons? 1969 191.0 170.00 1500 1400 1920 1700 1100 100 100 600 500 400 300 100 77.3146 YO'LL 76.6755 29 25.4179 9.8480
Please show calculations for the corresponding number of hydrogens for each peak cluster on the 1H NMR spectrum. Label a
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