Based on the following spectroscopic data of an unknown compound with molecular formula C8H6S, (i) determine the chemical structure of this compound; (ii) assign all the signals in the 1H-NMR spectrum & 13C-NMR spectrum. NMR is complete
Based on the following spectroscopic data of an unknown compound with molecular formula C8H6S, (i) determine...
) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure for this compound in the box at the bottom of the page. Peak assignments written on the spectra may be worth partial credit. (5 marks) r IR Spectrum liquid film) 1735 1717 4000 3000 1200 800 2000 1600 V (cm) 13C NMR Spectrum (100 MHz, CDCI, solution) DEPT CHI Chit Cht solvent proton decoupled 100 no Sloml proton decoupled 200 160 120 80 40...
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,...
need help elucidating please IR Spectrum (KBr disc) 4000 3000 2000 1600 1200 800 V (cm') UV Spectrum 100 Amax 310 nm log10 3.3) Mass Spectrum 80 mex 261 nm (log.oe 4.3) 120 60 solvent: methanol M 199/201 40 max 262 nm (log,0E 3.0) pa 257 nm (logE 3.0) Amax 222 nm 0og0 4.0) 155/157 20 184/186 40 280 80 200 240 120 160 solvent: methanol / HC m/e 13C NMR Spectrum (500 MHz, CDCI, solution) DEPT CH, CHt CH...
need help elucidating this please IR Spectrum Ker disc) 4000 3000 1600120080000 2000 v (cm ) Mass Spectrum 0.5 1.0F Soft UV spectrum 1032 mg/10mis path length: 1.00 solvent: cyclohen 1.5... 350 40 80 200 240 280 160 /e 200 120 m 250 300 2. (nm) 13C NMR Spectrum (1000 MHZ. CDCI, solution) DEPT Chich cht proton decoupled 40 08 (ppm) 80 200 160 120 'H NMR Spectrum (400 MHz, CDCI, solution) 3 2 1 4 5 6 7 TO...
Use the spectral data provided to determine the structure of the following organic conpounds. IR Spectrum ouid im) 3410 4000 3000 2000 1600 1200 V (om: 800 100 Mass Spectrum 43 80 60 M (15) 71 20 40 120 80 160 200 240 280 m/e 13C NMR Spectrum (50.0 M, COCI, solution) DEPT CHt CH,t CHt solvent proton decoupled 0 8 (ppm) 40 80 120 200 160 'H NMR Spectrum (200 MHz, CDCI, solution) expansion exchanges with Dy0 50 pom...
need help elucidating this please IR Spectrum KB ) 800 0.0 1200 4000 3000 2000 1600 V emi) Mass Spectrum Sofbose pak UN spectrum 15 mg/100 ml path length: 02 om solvent: ethanol 1 1.56 200 350 40 80 240 200 120 m 200 160 /e 250 300 2. (nm) 13C NMR Spectrum (50.0 MHz, CDCI, solution) Resolves into two signals at higher field DEPT Chat Chat Cht - Resolves into two signals at higher field solvent proton decoupled 0...
determine the compound structure based on the spectrums. please explain. IR Spectrum liquid rim) 1600 1200 800 4000 3000 2000 V (cm') 100 콩2 No significant LV absorption above 220 nm 40 3 C6H1004 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (S0.0 MH, CDC, solution) proton decoupled 40 0 δ(ppm) 200 160 120 80 H NMR Spectrum (200 MHz, CDCi solution) 10 9 8 76 5 4 3 2 1 0 8 (ppm)
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...
BONUS (10 pts) Determine the compound structure based on the spectra below. Annotate spectra to receive full credit 3457 IR Spectrum (CHCI solution) 4000 3000 2000 V (cm 1600 ) 1200 800 Mass Spectrum TY of base peak UV Spectrum 2 max 263 nm (1090€ 3.9) 2 max 305 nm (10910€ 2.1) solventi hexane 40 80 200 240 280 120 160 m/e Q Search BC NMR Spectrum (100.0 MH, CDC, solution) DEPT CH CH cht profon decoupled 200 8 (ppm)...
Amswer all parts please QUICKLY 6. Use the spectral data given to identify the structure of the unknown compound with chemical formula (C12H1602). (20 points) TOODE UV Spectum: 2 = 240 nm MW = 192 g/mol, ( Ombre HH2DSIMH IR resonance: 1610, 1729 cm', 13C NMR Spectrum (1000 MHz, CDCI, solution) DEPT CH CH CH proton decoupled solvent 200 160 120 B0 40 08 (ppm) TH NMR Spectrum (400 MHZ COCI, solution) expansion 9 8.0 7.5 PPM 10 9 8...