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Label spectra and propose a structure for the compound. Compound 1 IR Spectrum liquid mi 4000 3000 2000 1600 1200 12...
Label the spectra and propose a structure for the compound. Compound 1 IR Spectrum liquid mi...
Label the spectra and propose a structure for the compound.
Compound 1 IR Spectrum liquid mi 4000 3000 2000 1600 1200 1200 V on Mass Spectrum UV Spectrum 2. max 252 mm (10910622) 2. max 257 nm (log, 2.3) 2 mar 262 nm (10910€ 2.2) 2. max 254 nm (1090€ 2.2) 2.mex 268 nm logo 2.0) solvent thanol M 150 Coto2 40 80 240 120 m 200 280 160 /e 13C NMR Spectrum (100 M-2. CDC, solution ansion DEPT CH...
need help elucidating IR Spectrum 4000 3000 2000 V (cm 1500 1600 ) 1200 1200 800 UV Spectrum Mass Spectrum of base...
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...
need help elucidating please IR Spectrum (KBr disc) 4000 3000 2000 1600 1200 800 V (cm') UV Spectrum 100 Amax 310 n...
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...
BONUS (10 pts) Determine the compound structure based on the spectra below. Annotate spectra to receive...
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)...
Label the spectra and propose a structure for the compound. Compound 6 1 1755 IR Spectrum...
Label the spectra and propose a structure for the compound.
Compound 6 1 1755 IR Spectrum quid fim 1120 4000 3000 2000 V (cm 16001200800 ) Mass Spectrum So base peak M" 158 (<1%) No significant UV absorption above 220 nm C₂ H₂ 403 280 40 80 120 160 200 240 13C NMR Spectrum 150.0 MHz, CDCI, solution) DEPT Chut Chitch! proton decoupled 200 160 120 80 40 0 8 (ppm) TH NMR Spectrum 2200 MHZ. CDC, solution) 150 10...
determine the compound structure based on the spectrums. please explain. IR Spectrum liquid rim) 1600 1200...
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)
Label the spectra and propose a structure for the compound. Compound 4 IR Spectrum hould 4000...
Label the spectra and propose a structure for the compound.
Compound 4 IR Spectrum hould 4000 3000 17000 2000 2000 V (cm 1600 ) 1200 800 Mass Spectrum TTTTTTTT Sofhose pas No significant UV absorption above 220 mm M 100 CHOO 0 120 180 200 200 200 13C NMR Spectrum (1000 MHCOCI, solution DEPT CHICK CH proton decoupled 200 160 120 80 40 0 (ppm) "H NMR Spectrum (400 MHE. CDC, solution 10 9 8 7 6 5 4 3...
Problem 79 4000 3000 2000 1600 1200 800 V (cm) Mass Specrum uv Spectrum 100 80...
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
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...
Label the spectra and propose a structure for the compound.
Compound 1 IR Spectrum liquid mi 4000 3000 2000 1600 1200 1200 V on Mass Spectrum UV Spectrum 2. max 252 mm (10910622) 2. max 257 nm (log, 2.3) 2 mar 262 nm (10910€ 2.2) 2. max 254 nm (1090€ 2.2) 2.mex 268 nm logo 2.0) solvent thanol M 150 Coto2 40 80 240 120 m 200 280 160 /e 13C NMR Spectrum (100 M-2. CDC, solution ansion DEPT CH...
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...
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...
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)...
Label the spectra and propose a structure for the compound.
Compound 6 1 1755 IR Spectrum quid fim 1120 4000 3000 2000 V (cm 16001200800 ) Mass Spectrum So base peak M" 158 (<1%) No significant UV absorption above 220 nm C₂ H₂ 403 280 40 80 120 160 200 240 13C NMR Spectrum 150.0 MHz, CDCI, solution) DEPT Chut Chitch! proton decoupled 200 160 120 80 40 0 8 (ppm) TH NMR Spectrum 2200 MHZ. CDC, solution) 150 10...
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)
Label the spectra and propose a structure for the compound.
Compound 4 IR Spectrum hould 4000 3000 17000 2000 2000 V (cm 1600 ) 1200 800 Mass Spectrum TTTTTTTT Sofhose pas No significant UV absorption above 220 mm M 100 CHOO 0 120 180 200 200 200 13C NMR Spectrum (1000 MHCOCI, solution DEPT CHICK CH proton decoupled 200 160 120 80 40 0 (ppm) "H NMR Spectrum (400 MHE. CDC, solution 10 9 8 7 6 5 4 3...
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
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...
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