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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 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 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 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...
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)
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)
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,...
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 4 Da- U6)+20 IR Spectrum Oquid fim) 1760 800 1200 2000 1600 3000 4000 v (cm) Mass Spectrum 100 43 No significant UV absorption above 220 nm M146 (1% ) 87 20 CH1004 280 40 80 120 m/e 160 200 240 13C NMR Spectrum (1000 MHz,...
5. The spectral data provided below are for a compound with a molecular weight of 1 94 g/mol. Outline your interpre...
5. The spectral data provided below are for a compound with a molecular weight of 1 94 g/mol. Outline your interpretation of the data in point form and from your points, propose a structure consistent with the spectral data provided IR Spectrum (quid fim) 1712 1277 1254 L.... 800 2000 1600 V (cm) 1200 4000 3000 C NMR Spectrum Resolves into two signals at higher feld solvent proton decoupled o 8(ppm) 160 120 80 40 200 H NMR Spectrum (200...
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...
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...
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 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 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 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...
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)
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)
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,...
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 4 Da- U6)+20 IR Spectrum Oquid fim) 1760 800 1200 2000 1600 3000 4000 v (cm) Mass Spectrum 100 43 No significant UV absorption above 220 nm M146 (1% ) 87 20 CH1004 280 40 80 120 m/e 160 200 240 13C NMR Spectrum (1000 MHz,...
5. The spectral data provided below are for a compound with a molecular weight of 1 94 g/mol. Outline your interpretation of the data in point form and from your points, propose a structure consistent with the spectral data provided IR Spectrum (quid fim) 1712 1277 1254 L.... 800 2000 1600 V (cm) 1200 4000 3000 C NMR Spectrum Resolves into two signals at higher feld solvent proton decoupled o 8(ppm) 160 120 80 40 200 H NMR Spectrum (200...
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...
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...
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