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4. Determine the structure for the compound that has the following MS, IR and 'H-NMR spectra and explain the reason...
4. Determine the structure of an unknown compound whose mass, IR, and 'H-NMR spectra are shown below.. MS 100 43 71 Structure of the unknown compound 50 114 0 40 60 80 100 120 m/z IR H-NMR δ (ppm) 0
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...
5-A compound (CH40) has the following 1H NMR, 13C NMR, and IR spectra. Propose a structure consistent with this data. Part marks are available so show your work! Clearly indicate your final proposed structure (10 Marks) C8H140 TOO -140 SI 30 3000 1000 2000 1000 Warenumbers (cm) 200 180 160 140 120 100 80 60 40 20 ppm ketone ble 1530 1510 1500 H 5.0 4.5 4.0 3.5 3.0 2.5 2.0 15 pm 4
Deduce the following structure of the compound given their IR, H1 NMR, 13C NMR spectra, and assign IR functional group absorptions and assign the structure's protons and carbons to their respective spectral resonances. Compound 4 Da- U6)+20 IR Spectrum Oquid fim) 1760 800 1200 2000 1600 3000 4000 v (cm) Mass Spectrum 100 43 No significant UV absorption above 220 nm M146 (1% ) 87 20 CH1004 280 40 80 120 m/e 160 200 240 13C NMR Spectrum (1000 MHz,...
A compound with molecular formula C11H140 displays the following IR, H NMR and 13C NMR spectra. Propose a structure for this compound 180 20.200 160 0 120 100 06 60 40 20 PPM
Use IR, proton NMR and MS data to deduce the correct structure. Draw the structure and circle it. Indicate on the IR, NMR and MS spectra the information you got from each to deduce the structure. 14, IR Spectrum 4000 3000 2000 V (cm 16001200800 ) Mass Spectrum 121/123 % of base peak M+-- 200202/204 X X or C₂ H₂ Brz 240 280 40 80 120 160 m/e 200 'H NMR Spectrum (400 MHz, CDCI, solution) triplet expansions carbon Carbon...
A compound with molecular formula C7H1402 displays the following IR, 'H NMR and 13C NMR spectra. Propose a structure for this compound. 1 300 VEN 2 2. HSP-00-388 ppm 180 160 100 120 100 ab 66 40 20 PPM
The compound that gives the following IR, 'H-NMR and Deduce the structure? Explain. C-NMR spectra has the formula C H1602 5H, m 3H. d 1H, quartet *760 140 120 100 30 86 46
Compound 2: Use the information provided below and the IR and NMR spectra on the next page to answer the following questions. a) An MS was taken of compound 2 and the table is given below. Determine the molecular formula of 2 from the MS given below relative abundance m/z 132 100 133 9.8 b) Calculate the Index of Hydrogen Deficiency/Degree of Unsaturation for the molecule. c) Using the IR spectrum and the 1H- and 13C-NMR spectra given below, determine...