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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 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)
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...
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...
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...
Label the spectra and propose a structure for the compound. The IR spectra are listed in...
Label the spectra and propose a structure for the compound.
The IR spectra are listed in the translation.
Compound 2 R Spectrum Medisch 3400 1720 4000 3000 1600 vomi) 1200 183 Mass Spectrum So base UV Spectrum mas 253 nm 109,9€ 2.6) homas 250 nm 109,96 2.7) ho mar 284 m 109,0 2.5) M -220N) CH2O| 280 40 80 120 160 200 240 13C NMR Spectrum (100 . CDC, DEPT CH CH CH protondeco 200 160 1 20 80 400...
Label the spectra and propose a structure for the compound. Compound 3 IR Spectrum quid 4000...
Label the spectra and propose a structure for the compound.
Compound 3 IR Spectrum quid 4000 3000 2000 V (cm 1000 ) 1200 800 of base peak more Cg H100 280 40 80 120 160 200 240 C NMR Spectrum 50. 0 00, DEPT Chi sont on GGL 200 160120 120 80 40 0 5 (ppm) TH NMR Spectrum (200 M . CDCI, solution 10 9 8 7 6 5 4 3 2 i 8 (ppm)
Label spectra and propose a structure for the compound. Compound 1 IR Spectrum liquid mi 4000 3000 2000 1600 1200 12...
Label 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 chut...
Please label all spectra for C5H9O2Br Problem 2 IR Spectrum liquid film) 1740 4000 3000 2000...
Please label all spectra for
C5H9O2Br
Problem 2 IR Spectrum liquid film) 1740 4000 3000 2000 1600 V (cm) 1200 600 Mass Spectrum قليلالالالالالا % of base peak No significant UV absorption above 220 nm 107/109 152/154 M + 180/182 C5H,OBr 40 80 200 240 120 160 m/e 280 . 13C NMR Spectrum (50,0 MHz, CDCI, solution) DEPT CH CH CH4 proton decoupled solvent 200 160 120 80 OLII 40 08 (ppm) TH NMR Spectrum (300 MHz, CDCI, solution) expansion...
Label the spectra and propose a structure for the compound. Compound 2 R Spectrum Bedie 3400...
Label the spectra and propose a structure for the compound.
Compound 2 R Spectrum Bedie 3400 1720 4000 3000 2004 1600 vomi) 1200 800 183 Mass Spectrum Softbase de UV Spectrum . mar 253 nm 109,96 26) mas 250 nm 109,2.7) 2 mar 284 m 109,0 2.5) M -220N) CH2O 280 40 80 120 160 200 240 13C NMR Spectrum (100 . CDC, DEPT CH Chicht protondeco 200 160 120 80 400 (ppm) 'H NVR Spectrum (400MCDO, Exchanges wayo Exchanges...
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...
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)
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...
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...
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...
Label the spectra and propose a structure for the compound.
The IR spectra are listed in the translation.
Compound 2 R Spectrum Medisch 3400 1720 4000 3000 1600 vomi) 1200 183 Mass Spectrum So base UV Spectrum mas 253 nm 109,9€ 2.6) homas 250 nm 109,96 2.7) ho mar 284 m 109,0 2.5) M -220N) CH2O| 280 40 80 120 160 200 240 13C NMR Spectrum (100 . CDC, DEPT CH CH CH protondeco 200 160 1 20 80 400...
Label the spectra and propose a structure for the compound.
Compound 3 IR Spectrum quid 4000 3000 2000 V (cm 1000 ) 1200 800 of base peak more Cg H100 280 40 80 120 160 200 240 C NMR Spectrum 50. 0 00, DEPT Chi sont on GGL 200 160120 120 80 40 0 5 (ppm) TH NMR Spectrum (200 M . CDCI, solution 10 9 8 7 6 5 4 3 2 i 8 (ppm)
Label 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 chut...
Please label all spectra for
C5H9O2Br
Problem 2 IR Spectrum liquid film) 1740 4000 3000 2000 1600 V (cm) 1200 600 Mass Spectrum قليلالالالالالا % of base peak No significant UV absorption above 220 nm 107/109 152/154 M + 180/182 C5H,OBr 40 80 200 240 120 160 m/e 280 . 13C NMR Spectrum (50,0 MHz, CDCI, solution) DEPT CH CH CH4 proton decoupled solvent 200 160 120 80 OLII 40 08 (ppm) TH NMR Spectrum (300 MHz, CDCI, solution) expansion...
Label the spectra and propose a structure for the compound.
Compound 2 R Spectrum Bedie 3400 1720 4000 3000 2004 1600 vomi) 1200 800 183 Mass Spectrum Softbase de UV Spectrum . mar 253 nm 109,96 26) mas 250 nm 109,2.7) 2 mar 284 m 109,0 2.5) M -220N) CH2O 280 40 80 120 160 200 240 13C NMR Spectrum (100 . CDC, DEPT CH Chicht protondeco 200 160 120 80 400 (ppm) 'H NVR Spectrum (400MCDO, Exchanges wayo Exchanges...
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...
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