Find the chemical structure using the wave spectrum shown Problem 11.4 100 40 40 Exact M.9. (EI)-98.0732 FT-IR (NEAT...
Use the following wave spectrum to identify the chemical structure Problem 11.10 60 40 Exact M.S. (CI) 129.1279 FT-IR (NEAT) 20 UVAmax BLANK 4000 3000 2000 800 WAVENUMBERS (CM) 1200 1000 100. Mass Spec. CI 70eV 60 55 40 43 129 20 40 60 70 80 100 110 120 40 m/s 13C NMR 62.3 MHz COCI CDCI luuluuluu 50 40 30 20 10 120 S00 70 130 160 150 140 170 H 500 MHz 3H CDCla 5.2 Hz/mm H 10H...
Find the chemical structure using the wave spectrum shown Problem I1.3 40 Exact M.S. (E)- 84.0575 UVAmax-209 (E-16,000) 328 (E-50) FT-IR (NEAT) 20 3000 2000 WAVENUMBERS (CM) 1800 1200 100 Mass Spec. El 70eV 40 20 50 40 44 55 70 m/z T 13C NMR 62.3 MHz COCla D D 192 11 190 CDCI Fwwwwluuluuluulnluulululul luulnluuluuluulun ad 0 ppm 0 HE 150 120 100 120 160 150 140 130 110 50 50 40 20 10 250 10 Ha/dw 250 MHz...
Mass Spectrum (not shown): [M] = 220 (75%), 222 (100%), 224 (25%) m/z IR Spectrum (not shown): 3060, 2985, 1600, 1495 cm-1 (all listed are strong (s) unless otherwise indicated) Please explain how you determine the organic compound for the info given. Please check your compound with Chemdraw to verify your answer before posting your answer (if you have Chemdraw). Thanks! NMR Spectrum (400 MHz, CDCI, 25 C) t (J 8Hz) PPM 1H1H 1H 3H C NMR Spectrum (with DEPT,...
Find the compounds using NMR and IR: Problem 85 IR Spectrum (liquid fiim) 1720 1600 2000 v (cm) 800 3000 1200 4000 100 Mass Spectrum 73 140 138 80 No significant UV 60 115 absorption above 220 nm 40 M 194/196 (1% ) 20 CeH1102Br 120 160 200 240 280 40 80 m/e 13C NMR Spectrum (50.0 MHz, CDCI, solution) DEPT CH, Cн, сн! solvent proton decoupled 8 (ppm) 160 120 40 200 80 H NMR Spectrum (200 MHz, CDCI,...
Find the compounds using IR and NMR: Problem 25 2251 IR Spectrum (liquid film) 800 1600 1200 4000 3000 2000 v (cm) 100 Mass Spectrum M 117 80 77 60 91 40 20 CgH7N 200 80 120 160 240 280 40 m/e expansion 13C NMR Spectrum (100.0 MHz, CDCI, solution) 130 129 ppm DEPT CH Cн,! сн! expansion 130 129 ppm solvent proton decoupled (ppm) 40 200 160 120 80 H NMR Spectrum (400 MHz. CDCI, solution) TMS 10 7...
Please draw the unknown molecule presented in the specs, Thanks!!! Mass Spectrum (not shown): [M] = 169 (100%) m/z IR Spectrum (not shown): 2985, 2250 (m), 1745 cm1 (all listed are strong (s) unless otherwise indicated) H NMR Spectrum (400 MHz, CDC I3, 25 °C) 5 3 PPM 2H 2H 2H 6H 3H C NMR Spectrum (with DEPT), proton-decoupled (125 MHz, CDCI3, 25 °C) (CH2) (C) (CH3) (CH2) (CH3) (C) (C) (CH2) 180 160 80 140 120 100 PPM 60...