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help me with the structure please
i can't find the right structure. please help
IR Spectrum...
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)
Problem 3 IR Spectrum (quam 4000 3000 2000 1600 V (cm) 1200 800 Mass Spectrum So...
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)
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,...
need help elucidating this please IR Spectrum 4000 2000 V (cm 1600 ) 1200 Mass Spectrum...
need help elucidating this please
IR Spectrum 4000 2000 V (cm 1600 ) 1200 Mass Spectrum M 110 WoW UV Spectrum 2. 225 mm (0, 2 276 nm (109, 2 283 nm (109, 3.5) 3.4) 3.3) الامام للتفاعل solvent methanol 40 80 120 160 200 240 280 13C NMR Spectrum 1100 MHE COCI, solution) DEPT Chat Cast cht prolon decoupled 0 40 (ppm) 16012080 200 TH NMR Spectrum (400M , CDC, solution) expansion Exchanges with D20 4 3 2 1...
Attached are four spectra for isomer with the MF= c12h14o4. Determine the structure for each molecule...
Attached are four spectra for isomer with the MF=
c12h14o4. Determine the structure for each molecule and draw them
below.
problem 63 IR Spectrum (CCI, solution) 1765 4000 3000 1200 800 2000 V (cm ) Mass Spectrum UV Spectrum & 8 8 g 8 of base 2 mar 269 nm (10910€ 2.7) humax 263 nm (10910 2.7) M -222 (< 1) 169 sahent: methanol 8 C12H1404 240 280 40 80 120 160 200 13C NMR Spectrum (50.0 MHz, COCI, solution)...
Label the spectra and propose a structure for the compound. Compound 5 IR Spectrum Olquid fim...
Label the spectra and propose a structure for the
compound.
Compound 5 IR Spectrum Olquid fim 1740 4000 3000 20 ,1600 1200 300 100% Mass Spectrum M = 150/152 (15) CH,40, CI 240 280 40 80 120 160 200 13C NMR Spectrum (500 M , CDC, son DEPT CH CH CH selvon proton decoupled 200 160 120 80 40 0 8 (ppm) 'H NMR Spectrum (200 MH. COCI, solution 10 9 8 7 6 5 4 3 2 (ppm)
Identify Structure Problem 121 ཀ་ IR Spectrum (KBr disc) 1728 4000 3000 1200 800 2000 1600...
Identify Structure
Problem 121 ཀ་ IR Spectrum (KBr disc) 1728 4000 3000 1200 800 2000 1600 V (cm) 57 Mass Spectrum 98 100F 80 60 4043 20 of base peak No significant UV absorption above 220 nm M-154 139 Co Higo 40 80 200 240 280 120 160 mle 13C NMR Spectrum (100.0 MH2, CDCI, solution) expansion DEPT CH CH. CH 28 27 ppm expansion solvent proton decoupled 27 pm 200 160 120 80 40 0 8 (ppm TH NMR...
Deduce the following structure of the compound given their IR, H1 NMR, 13C NMR spectra, and...
Deduce the following structure of the compound given their IR, H1
NMR, 13C NMR spectra, and assign IR functional group absorptions
and assign the structure's protons and carbons to their respective
spectral resonances.
Compound 6 1756 IR Spectrum uid Sm) 15820 4000 3000 2000 1600 1200 800 V (cm) 100 55 Mass Spectrum 71 80 70 60 No significant UV M158 (1%) absorption above 220 nm C&H140s 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz,...
Problem 4 IR Spectrum ud 1600 LL 4000 2000 1600 1200 800 Mass Spectrum 131 عقل مقلمتململمعلم So base peske 103 M CHO...
Problem 4 IR Spectrum ud 1600 LL 4000 2000 1600 1200 800 Mass Spectrum 131 عقل مقلمتململمعلم So base peske 103 M CHO 280 40 80 120 160 200 240 13C NMR Spectrum M CDO, Rewives DEPT CHẢ CHỊ CHẾ expansion is higher ed proton decoupled 200 160 120 06 (ppm) "H NMR Spectrum (200 MHz, CDCI, solution) expansion 10 9 8 7 2 1 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
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)
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)
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 this please
IR Spectrum 4000 2000 V (cm 1600 ) 1200 Mass Spectrum M 110 WoW UV Spectrum 2. 225 mm (0, 2 276 nm (109, 2 283 nm (109, 3.5) 3.4) 3.3) الامام للتفاعل solvent methanol 40 80 120 160 200 240 280 13C NMR Spectrum 1100 MHE COCI, solution) DEPT Chat Cast cht prolon decoupled 0 40 (ppm) 16012080 200 TH NMR Spectrum (400M , CDC, solution) expansion Exchanges with D20 4 3 2 1...
Attached are four spectra for isomer with the MF=
c12h14o4. Determine the structure for each molecule and draw them
below.
problem 63 IR Spectrum (CCI, solution) 1765 4000 3000 1200 800 2000 V (cm ) Mass Spectrum UV Spectrum & 8 8 g 8 of base 2 mar 269 nm (10910€ 2.7) humax 263 nm (10910 2.7) M -222 (< 1) 169 sahent: methanol 8 C12H1404 240 280 40 80 120 160 200 13C NMR Spectrum (50.0 MHz, COCI, solution)...
Label the spectra and propose a structure for the
compound.
Compound 5 IR Spectrum Olquid fim 1740 4000 3000 20 ,1600 1200 300 100% Mass Spectrum M = 150/152 (15) CH,40, CI 240 280 40 80 120 160 200 13C NMR Spectrum (500 M , CDC, son DEPT CH CH CH selvon proton decoupled 200 160 120 80 40 0 8 (ppm) 'H NMR Spectrum (200 MH. COCI, solution 10 9 8 7 6 5 4 3 2 (ppm)
Identify Structure
Problem 121 ཀ་ IR Spectrum (KBr disc) 1728 4000 3000 1200 800 2000 1600 V (cm) 57 Mass Spectrum 98 100F 80 60 4043 20 of base peak No significant UV absorption above 220 nm M-154 139 Co Higo 40 80 200 240 280 120 160 mle 13C NMR Spectrum (100.0 MH2, CDCI, solution) expansion DEPT CH CH. CH 28 27 ppm expansion solvent proton decoupled 27 pm 200 160 120 80 40 0 8 (ppm TH NMR...
Deduce the following structure of the compound given their IR, H1
NMR, 13C NMR spectra, and assign IR functional group absorptions
and assign the structure's protons and carbons to their respective
spectral resonances.
Compound 6 1756 IR Spectrum uid Sm) 15820 4000 3000 2000 1600 1200 800 V (cm) 100 55 Mass Spectrum 71 80 70 60 No significant UV M158 (1%) absorption above 220 nm C&H140s 40 80 120 160 200 240 280 m/e 13C NMR Spectrum (50.0 MHz,...
Problem 4 IR Spectrum ud 1600 LL 4000 2000 1600 1200 800 Mass Spectrum 131 عقل مقلمتململمعلم So base peske 103 M CHO 280 40 80 120 160 200 240 13C NMR Spectrum M CDO, Rewives DEPT CHẢ CHỊ CHẾ expansion is higher ed proton decoupled 200 160 120 06 (ppm) "H NMR Spectrum (200 MHz, CDCI, solution) expansion 10 9 8 7 2 1 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
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