Answer Happy

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.).
24.44 7.0 H-NMR 36.51 38.44 t S 89 C4H802 Degrees of unsaturation: 1 o's 24.9% 24.98 07 9 b ONE CH2 SE CH3 H3C O'T 120 110 10.0 9. 80 7.0 5.0 3.0 1.0 -2.0 YY 7.200 POZIT 4.1936 4.0953 2.0360 1.6090 1.250Z 1.2330 1.2107 6810E

C4H802 C-NMR 4 unique carbons? 1900 1800 17 00 1500 14.0 101 110 100.0 W0100, 4000 4000 MO 100 L3109 SIST 72.000 746758 38.7339 TTSTE FRE