Problem 50 IR Spectrum 2000 1600 1200 800 V (cm) Mass Spectrum 80 No significant UV...
Problem 19 IR Spectrum 2000 1600 1200 800 100 Mass Spectrum No significant UV absorption above 220 nm 40 M+ 147149 40 80 120 160 200 240 280 m/e 3C NMR Spectrum (100 MHE, CDC, solution) proton decoupled 200 160 120 40 0 8(ppm) H NMR Spectrum 22 ppm 8 5 2 δ(ppm)
Problem 79 4000 3000 2000 1600 1200 800 V (cm) Mass Specrum uv Spectrum 100 80 60 40t 3 20 max 260 nm (logroE 2.5) 91 solvent: methanol C11H16 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz, CDC, solution) proton decoupled 200 160 120 40 0 δ(ppm) H NMR Spectrum (200 MHz, CDci, solution) 7.5 7.0 ppm
need help eluciadting this please IR Spectrum 4000 3000 2000 V (cm 1600 ) 1200 800 Mass Spectrum No significant UV absorption above 220 mm 120 160 200 240 280 13C NMR Spectrum (1000 ML. COCI, solution DEPT CH CH cht proton decoupled 40 08 (ppm) 80 120 200 160 expansion "H NMR Spectrum 400 MHE. CDCI, solution 3.6 ppm 3 2 1 4 5 7 6 0 8 (ppm) 10 9 8
need help elucidating this please IR spectrum 4000 3000 1200 800 2000 V (cm 1600 ) Mass Spectrum No significant UV absorption above 220 mm 101 M 40 80 120 160 200 240 280 13C NMR Spectrum (1000MCDC, DEPT CHICH.CH proton decoupled 200 160 120 80 40 0 (ppm) 'H NMR Spectrum (400 MHz, CDCI, solution) expansion 10 PPM 10 9 8 7 6 5 4 3 2 1 8 (ppm)
Problem 3 IR Spectrum (quam 4000 3000 2000 1600 V (cm) 1200 800 Mass Spectrum So base per 107/109 152/54 M 180/182 CgH9O2Br 40 80 120 160 mle 200 240 280 13C NMR Spectrum (50.0 CDC, on DEPT CHIC CHA over proton decoupled 200 160 120 80 400 8 (ppm) 'H NMR Spectrum (200 M COCI, solution 40 pm 10 9 8 7 6 5 4 3 2 8 (ppm)
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 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 IR Spectrum 4000 3000 2000 V (cm 1500 1600 ) 1200 1200 800 UV Spectrum Mass Spectrum of base peak 2 max 310 nm (og 3.3) 2 max 261 nm (10970€ 43) solvent methanol 199201 15515 184186 2. max 262 nm (09/0€ 3.0) 1. max 257 nm (1090€ 3.0) max 222 nm (log,o€ 4.0) 80 120 160 200 240 280 so m ethane/HGI m / 13C NMR Spectrum (500 M . CDCI, solution) DEPT CH CH. CH...
do the spec problem Problem 9 IR Spectrum (kuid im) 0.0 800 1600 1200 2000 V (cm) 3000 4000 Mass Spectrum 0.5F 100 80 60 UV spectrum 1,0 77 107 5.815 mg/ 10 mls path length: 1.00 cm solvent: ethanel M 122 20E 1.5 300 350 250 200 200 280 240 120 160 40 80 (nm) m/e 13C NMR Spectrum Aath (20.0 MHz, CDCI, solution) expansion x5 off-resonance decoupled proton decoupled 200 160 120 80 8 (ppm) 40 0 1H...
solve for the unknown molecular structure. #2 IR Spectrum iquid m 1740 2000 v (em) 800 3000 1600 1200 4000 100 Mass Spectrum 80 No significant UV absorption above 220 nm 5e M116 (1%) 73 C&H1202 120 160 m/e 40 80 200 240 280 13C NMR Spectrum (20.0 MHz, CDa, solution) -CH C-H -CH TMS solvent proton decoupled 200 160 120 80 40 8 (ppm) H NMR Spectrum (100 MHr, CDC, soluon) 20 Hz aas pom 192 ppm 0.03 Pem...