Please show calculations for the corresponding number of hydrogens for each peak cluster on the 1H NMR spectrum. Label a

[answerhappygod]

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.).

Please Show Calculations For The Corresponding Number Of Hydrogens For Each Peak Cluster On The 1h Nmr Spectrum Label A 1 (18.11 KiB) Viewed 35 times

20 Για 101.3 t C6H15N H-NMR Degrees of unsaturation: 0 Oz 65.72 65.2 9 CH3 NH CH3 10 CH CH CH3 CH3 590- 12.0 11.0 10,6 9.0 8.0 7.0 6.0 5.0 40 30 2,8 -1.0 -2.0

C6H15N C-NMR 2 unique carbons? AS 1.6 T U 9 10 12 13 14 15 16 17 18 19 20 21 22 23 ΓΟ ΤΟ 001 19.0 10.0 1700 160.6 100 1400 120.0 120.0 110.000 900 90.0 0.0 0.0 0.0 0.0 20.0 100 77.3342 76.6854 77.00 45.35 11.J449 アカ