Fall 2019 Problem 5 IR Spectrum (iquid fim) 1715 4000 3000 2000 V (cm) 1600 1200...
Fall 2019 Problem 5 IR Spectrum (quid fim) 1715 4000 3000 2000 1600 1200 V (cm) 800 100 44 80 Mass Spectrum 60 58 20 M 71 86 C5H100 40 80 280 120 240 160 200 13C NMR Spectrum (20.0 MMz, CDCI, solution) -сн, C-H proton decoupled TMS C-H solvent Jul. 5 (ppm) 0 120 80 160 200 1H NMR Spectrum (100 MHz, CDCI, solution) expansion of 400 MHz spectrum 20 Hz TMS 0.99 ppm 2.21 2.31 9.75 1 8...
Fall 2019 Problem 5 IR Spectrum LL 4000 1715 3000 2000 1600 V ( 1200 1200 600 Mass Spectrum مقلللللملللملا of bese peak C₂H00 280 40 80 120 160 200 240 TTTTTT 13C NMR Spectrum (20.0 CDCI, HĆ7 proton decoupled C-H solvent 200 160 120 80 400 (ppm) 'H NMR Spectrum 1900 MHE. COCI, solution) expansion of 400 spectrum 2.21 0.99 pm 9 8 7 6 5 4 3 2 1 (ppm)
Fall 2019 Problem 5 IR Spectrum Doud 4000 1715 3000 2000 V (cm 1600 ) 1200 800 Mass Spectrum of base peak CHOO 40 80 120 160 200 240 280 13C NMR Spectrum (20.0 MHE. COCI, solution H-C+ -CHE proton decoupled solvent 200 1601 160 80 08 (ppm) 'H NMR Spectrum 100 MH2 CDC, solution) expansion of 400 MHz spectrum 20 Hz 10 9 8 7 6 5 4 3 2 1 (ppm)
Fall 2019 Problem 5 IR Spectrum Doud 4000 1715 3000 2000 V (cm 1600 ) 1200 800 Mass Spectrum of base peak CHOO 40 80 120 160 200 240 280 13C NMR Spectrum (20.0 MHE. COCI, solution H-C+ -CHE proton decoupled solvent 200 1601 160 80 08 (ppm) 'H NMR Spectrum 100 MH2 CDC, solution) expansion of 400 MHz spectrum 20 Hz 10 9 8 7 6 5 4 3 2 1 (ppm)
Fall 2019 Problem 3 IR Spectrum (CHC solution) 1350 1170 4000 3000 800 2000 v (cm) 1600 1200 100 Mass Spectrum 91 80 M 200 60 155 40 172 20 Cg H1203S 240 280 200 120 m/e 160 80 40 13C NMR Spectrum (20.0 MHz, CDCI, solution) C-H C-H H-GH -CH -CH solvent TMS proton decoupled 0 8(ppm) 40 80 120 160 200 H NMR Spectrum (100 MHz. CDCI, solution) TMS 1 8 (ppm) 6 7 8 yeed % of...
7 Problems Fall 2019 Problem 5 IR Spectrum 4000 3000 2000 1600 V (cm ) 1200 Mass Spectrum TTTTTTT So base peak 171 M CHOO 40 80 120 160 200 240 280 13C NMR Spectrum (20.0 M CDO, HCH -CH proton decoupled solvent 200 160 120 80 40 0 S (ppm) 'H NMR Spectrum (100 MHZ, COCI, solution) expansion of 400 MHz spectrum 20 HZ 2.31 10 9 LLLLL 8 7 6 5 4 3 2 1 8 (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
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...
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)
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,...