provide the structure for the compound while using as much of the NMR/IR as possible. show...
provide the structure for the compound while using as much of thr NMR/IR as possible. show work. 28. (+)-Hl(aq); (20 pts) MFC MW 133 SC 69.5 SH 14 Na Spec. Data Copyright © 1994 2H 3H 2H 2H 150 140
provide the structure for the compound while using as much of thr NMR/IR as possible. show work. MP CH4 MW 110 SC3 SH 12.7 Mass Spes. De Copyright © 1994 Preton NM Carbon 13
provide the structure for the compound while using as much of thr NMR/IR as possible. show work.
provide the structure for the compound while using as much of the NMR as possible. show work. 26 29. C10H14 (20 pts) Pr NMR 7 integral values 129.2 129.2 20 PPM Cube
7. Consider the IR, 'H-NMR and C-NMR spectra of the compound with MFC,1,0, Identify the structure of the unknown compound MP pls MW 114 *C 73.6 WW 124 Mass Spee, D relativ mix bund, 27 71 74 LESTE WVELDEN Copyright © 1994 래 TTTT 2.0 3.0 Proton NMR 1.5 1.0 PPM MITTIT 200 TTI TITTI 80 60 40 20 PPM 0 180 160 Y 120 140 100 Carbon 13 NMA 8. Consider the IR, 'H-NMR and 13C-NMR spectra of the...
provide the structure for the compound while using as much of the NMR as possible. show work. 31. C2H2O (20 pts) 3.5 1.0 PPM 0.5 Pret NMR 20. integral values - 179 Cube 11 NMR
7. Consider the IR, 'H-NMR and C-NMR spectra of the compound with MF:C,H, 0. 4 pts Identify the structure of the unknown compound. MF C7H140 MW 114 $C 73.6 SH 12.4 Mass Spec. D m/ sbund. 27 35 relativ 114 11 Popyright © 1994 1.0 PPM 3.0 Proton NMA TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 200 180 160 140 Carbon 13 NMR T 120 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 100 80 60 40 20 PPM O en og and 8. Consider the IR, 'H-NMR and C-NMR spectra of the...
provide the structure for the compound while using as much of the NMRas possible. show work. 30. C7H140 (20 pts) Integral Values 220 200 Carton 13 NMR
This compound has the molecular formula CsHino. It is IR 'Hand 13C NMR spectra are show below 1. Write the functional group for every number in the IR, 2. calculate the integration for every peak in the 'H NMR 3. Write the kind of proton for every number in the proton NMR 4. Write the kind of carbon for every number in the 13C NMR. 5. Determine the structure, and show how it consistent with the observed absorptions. 100) 993...
8. IR and proton NMR spectra for compound X are given below. Propose a structure for compound X based on these spectral data. Assign major IR peaks and proton signals. 100+ 90 801 ME92 33AM 45 73 70 604 504 401 57 301 201 101 20 40 200 0 80 180 00 120 140 160