provide the structure for the compound while using as much of thr NMR/IR as possible. show...
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 the NMR/IR as possible. show work. 26. (-)-Br/CC (+)-Hl(aq)(20 pts) ether MP C6H1209 MW 132 SC 56.5 Mị an hệ | NHÀ Proton NC TFTTTTTTT 120 20 PM Carbon 13 NMR
provide the structure for the compound while using as much of thr NMR/IR as possible. show work.
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...
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...
assign the major absorptions in the IR spectra, assign chemical shifts in both NMR, designate the parent peak in the mass spectra data and assign the major fragments to their corresponding peaks, and finally provide the structure for the formula. MF C9H100 MW 134 SC 10.6 SH 7.5 Mass Spec. Data relative mit abund 5123 77 27 91 100 12 103 105 134 1357 Copyright © 1994 2H2H 2.8 2.PPK Proton NMR 215010 205 206 195 196 PPM Carbon 13...
An alcohol 6. Consider the IR, 'H-NMR and 13C-NMR spectra of the compound with MF: C,H, 0. Identify the structure of the unknown compound. 4 pts MF C7H160 MW 116 *C 72.3 %H 13.9 TS SSTT * TRANSMITTANCE Mass Spec. relati m/z abun 27 29 31 19 42 10 45 18 ze SCI 2870.23 Copyright © 1994 WAVENUMBERS WENUNTERS 124 9.612.5% Proton NMR 2.6 0.5 PPM 604020 PPM 1000 Carbon 13 NNA OH B. D. OH
assign the major absorptions in the IR spectra, assign chemical shifts in both NMR, designate the parent peak in the mass spectra data and assign the major fragments to their corresponding peaks, and finally provide the structure for the formula. MF CHE MW 68 %C88.2 *H 11.8 Mass Spec. Data relative m/ abund. 21 3H .. Copyright © 1994 Note 'long-range' coupling. T TTTTTTTTTTTTTTTTT 2.4 2.2 2.0 Proton NMR 1.8 1.6 1.4 1.0 0.8 PPM Carbon 13 NMR
18. 1. Provide degrees of unsaturation 2. Identify the IR peaks of interest. 3. Analyze, appropriately and sufficiently, the NMR peaks of interest. 4. Provide the structure. 5. Appropriately, identify the carbon-13 peaks, as alkyl, alkenyl, alkynyl, aromatic, carbonyl, etc. We were unable to transcribe this imageAVENUMBERS 3H Copyright © 1994 2H 2H 2H 2H 2 PPM Proton NMR 140 120 100 80 20 PPM Carbon 13 NMA
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