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Problem 2 000 8 Mass Som 8 8 8 2 CH, SN 50 120 160 200 240 280 C NMR Spectrum MCDO, DEPT OK out ont protondeco 200 1...
R Spec 2000 1800 1200 Mass Spectrum ws M" CH, 9,81 240 280 100 12 160 200 200 3C NMR Spectrum M CDO, DEPT ost 200 16...
R Spec 2000 1800 1200 Mass Spectrum ws M" CH, 9,81 240 280 100 12 160 200 200 3C NMR Spectrum M CDO, DEPT ost 200 160 1 20 08 (ppm) HNMR Spectrum 200 CDC, solo .0 10 9 8 8 (ppm)
Problem 5 S © H, BH 280 SC NMR Spectrum Sco, DEPT Citout protocoupled 200 160...
Problem 5 S © H, BH 280 SC NMR Spectrum Sco, DEPT Citout protocoupled 200 160 120 80 40 (ppm) 'H NMR Spectrum 200 CDC, expansion 8 (ppm)
3438 IR Spectrum 4000 3000 2000 1600 1200 300 von 1800 Mass Spectrum Sobese per 40 C₂ H₂O₂) 260 80 120 m 160 200 240...
3438 IR Spectrum 4000 3000 2000 1600 1200 300 von 1800 Mass Spectrum Sobese per 40 C₂ H₂O₂) 260 80 120 m 160 200 240 /e SC NMR spectrum MOC, DEPT OCH 200 160120 opom H NMR Spectrum 2200 M CDO, expansions 0,0 10 9 8 7 6 5 4 3 2 8 (ppm)
need help eluciadting this please IR Spectrum 4000 3000 2000 V (cm 1600 ) 1200 800 Mass Spectrum No significant UV...
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
Find the compounds using IR and NMR: Problem 25 2251 IR Spectrum (liquid film) 800 1600...
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...
Compound 2 IR Spectrum Chri) 4000 3000 2000 18001200 vom",000 1200000 100 Mass Spectrum UV Spectrum...
Compound 2 IR Spectrum Chri) 4000 3000 2000 18001200 vom",000 1200000 100 Mass Spectrum UV Spectrum M 220 (1) 2. max 253 nm 0091626) 2. max 250 nm (09, 2.7) 2. max 264 nm (09,06 2.5) PS.... CH2O3 solvent thanol 40 80 120 160 200 240 280 13C NMR Spectrum (100 MHE COCI, solution) DEPT CH CH CH proton decoupled 30 128 ppm 200 - 160 120 80 40 08 (ppm) 'H NMR Spectrum (400MHE. COCI, solution Exchanges wie Do...
Find the compounds using NMR and IR: Problem 85 IR Spectrum (liquid fiim) 1720 1600 2000...
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,...
Label the spectra and propose a structure for the compound. Compound IR Spectrum Olquid fim 1740...
Label the spectra and propose a structure for the
compound.
Compound IR Spectrum Olquid fim 1740 4000 3000 2000 1800 1200 800 100 Mass Spectrum yood M = 150/152 (15) CH40, CI 240 280 40 80 120 160 mle 200 13C NMR Spectrum (500 MG, COO, solo DEPT CH CH.CH selvon proton decoupled 200 160 120 80 40 0 (ppm) 'H NMR Spectrum (200 ML. COCI, solution) 10 9 8 7 6 5 4 3 2 1 (ppm)
help me with the structure please i can't find the right structure. please help IR Spectrum...
help me with the structure please
i can't find the right structure. please help
IR Spectrum ad 4000 2000 1800 1200 800 Mass Spectrum CHO 280 40 60 120 160 200 240 mle 13C NMR Spectrum (50.0 MH2 CDC, son WA DEPT CH CH. CH proton decoupled 200 16012080 400 (ppm) 'H NMR Spectrum (200 M CDO, O 10 9 8 7 6 5 4 3 2 6 (ppm) IR Spectrum udim 4000 3000 2000 1800 1200 300 Mass Spectrum...
need help elucidating this please IR Spectrum Ker disc) 4000 3000 1600120080000 2000 v (cm ) Mass Spectrum 0.5 1.0F...
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...
R Spec 2000 1800 1200 Mass Spectrum ws M" CH, 9,81 240 280 100 12 160 200 200 3C NMR Spectrum M CDO, DEPT ost 200 160 1 20 08 (ppm) HNMR Spectrum 200 CDC, solo .0 10 9 8 8 (ppm)
Problem 5 S © H, BH 280 SC NMR Spectrum Sco, DEPT Citout protocoupled 200 160 120 80 40 (ppm) 'H NMR Spectrum 200 CDC, expansion 8 (ppm)
3438 IR Spectrum 4000 3000 2000 1600 1200 300 von 1800 Mass Spectrum Sobese per 40 C₂ H₂O₂) 260 80 120 m 160 200 240 /e SC NMR spectrum MOC, DEPT OCH 200 160120 opom H NMR Spectrum 2200 M CDO, expansions 0,0 10 9 8 7 6 5 4 3 2 8 (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
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...
Compound 2 IR Spectrum Chri) 4000 3000 2000 18001200 vom",000 1200000 100 Mass Spectrum UV Spectrum M 220 (1) 2. max 253 nm 0091626) 2. max 250 nm (09, 2.7) 2. max 264 nm (09,06 2.5) PS.... CH2O3 solvent thanol 40 80 120 160 200 240 280 13C NMR Spectrum (100 MHE COCI, solution) DEPT CH CH CH proton decoupled 30 128 ppm 200 - 160 120 80 40 08 (ppm) 'H NMR Spectrum (400MHE. COCI, solution Exchanges wie Do...
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,...
Label the spectra and propose a structure for the
compound.
Compound IR Spectrum Olquid fim 1740 4000 3000 2000 1800 1200 800 100 Mass Spectrum yood M = 150/152 (15) CH40, CI 240 280 40 80 120 160 mle 200 13C NMR Spectrum (500 MG, COO, solo DEPT CH CH.CH selvon proton decoupled 200 160 120 80 40 0 (ppm) 'H NMR Spectrum (200 ML. COCI, solution) 10 9 8 7 6 5 4 3 2 1 (ppm)
help me with the structure please
i can't find the right structure. please help
IR Spectrum ad 4000 2000 1800 1200 800 Mass Spectrum CHO 280 40 60 120 160 200 240 mle 13C NMR Spectrum (50.0 MH2 CDC, son WA DEPT CH CH. CH proton decoupled 200 16012080 400 (ppm) 'H NMR Spectrum (200 M CDO, O 10 9 8 7 6 5 4 3 2 6 (ppm) IR Spectrum udim 4000 3000 2000 1800 1200 300 Mass Spectrum...
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...
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