The structure annotated is correct.
NMR problem. is my answer in the box correct? if not, what is the right answer...
Find the structure using NMR
C7H1402 TTTTTTTTTTTTTT 1.25 1.20 1.15 1.10 PPM.05 5. Proton NMR 4.5 4.5 4.0 1.0 PPM 43.5 12.9 Integral Values 77. 2 28.6 27.6 -- 71.6 1'61 - 9.3 173.7 68.8 31.7 - 22.5 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT 180 160 120 100 Carbon 13 NMR TTTTTTTTTT 20 PPM
Determine the structure using NMR.
CH1402 Nu. 4.0 Proton NMR 3.5 3.0 1.6 PPM 30.4 . integral values 50.3 - 18.9 TITT 160 166 140 120 100 20 PPM Carbon 13 NMR
PROBLEM 4 MW 150 72.0 SH 6.7 [10031-82 1994 2H 2H 10.09, Proton NMR 00 180 160 140 120 100 Carbon 13 NMR 20 PPM
Find the structure using NMR
C10H14 Proton NMR 7 1 PPM 58.0 19.6 integral values 46.6 -22.5 128.2 125.8 - 129.2 45.7 70E - - TT- TTTTTTTTTTTTTTTT 120 140 Carbon 13 NMR 100 20 PPM
Identify the structure and draw it based on the formula and the
spectroscopy. Justify your answer
MF CH40 47 MW 114 C 73.6 SH 12.4 3H 6H Copyright 1994 0.5 2.0 1.0 PPM 3.0 Poton NMR 2.5 1.5 180 160 140 200 80 120 100 20 PPM 0 Carbon 13 NMA ww ab sa ELITSM м М 6е 28 1500 180e 2000 2500 HAVENUMBERS 6H ЗН Copyright 1994 ST'S0T 1289.32 aL L9ET 20 89T 6L 8TLT ALE62 HAVENUMBERS ЗН ©1994...
Problem 112: treat the peaks at 2.3 ppm as two singlets, as the 1BC NMR confirms. Problem 112 IR Spectrum 4000 3000 2000 1600 1200 V (cm) Mass Spectrum uv Spectrum 100 A,s. 265 nm (log10ε 2.6) λ max 271 nm 0og10ε 2.6 ) M* 150 solvent: methanol 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (100.0 MHz, CDC, solution) 24 20 ppm 24 proton decoupled 200 160 120 80 40 δ (ppm) H NMR Spectrum 400...
problem 4.05 please
1-3. There are two sets of spectra attached. For each provide a structure and assign the peaks by labeling the structures and listing the peaks in the tables provided. 208 Label H NMR 6 Label C NMR 6 4.05 Label H NMR 8 Label C NMR 8 Problem 4.05 Given the spectroscopic data below (Proton, Carbon, gHSQC, gCOSY, and gHMBC), provide the structure of the molecule. (HR-MS: 238.1358 amu), {'H, 'H) Nuclear Overhauser effect correlation was observed...
Analyze the proton and carbon NMR for hexene
Prootn NMR hexene 1.967 3.88 -062 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 0.5 fi (ppm) Carbon NMR Hexene snowboy na pag may not be an anomanga boramahala naman po mula apabalintonpohumilitando un paloma hutwowa lan halangalawang bombando adopewa hawahanan tonton ompaauwbokay naponta w/w lugrad payun g taon tunay walang para el hogabypoint ben oylamatwaliwabommal Mamaannons 230 220 210 200190 180 170 160 150 140...
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...
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...