Label the spectra and propose a structure for the compound.
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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. 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 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 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 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...
In the boxes below, provide the structure of the compound that corresponds to each set of spectra...
In the boxes below, provide the structure of the compound that corresponds to each set of spectra on the next 5 pages. Be sure to show your work on the spectra for full credit. Account for all numbered peaks in the IR. In peaks if necessary. Assign all NMR spectra as completely as possible: number of NMR signals, integration, chemical shift, and splitting the mass spectrum, determine degrees of unsaturation and label 4 IR Spectrum 3000 2000 1 1600 1200...
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,...
Please solve for each spectra and solve the final compound. Problem 113 IR Spectrum 3000 1600...
Please solve for each spectra and solve the final compound.
Problem 113 IR Spectrum 3000 1600 200 V (cm) Mass Spectrum UV Spectrum ma 238 nm (42) Amax 281 nm (2.7) M 150 solvent: methanol CH1oO2 40 80 120 160 200 240280 m/e 13C NMR Spectrum (1000 M ???, solution) 325 130.0 Dom DEPT H Gtt proton decoupled 325 1300 ppm 200 160 120 80 40 ? (ppm) H NMR Spectrum 400 MHz Coc, solution) 80 79 73 72ppm TMS...
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.
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 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 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 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...
In the boxes below, provide the structure of the compound that corresponds to each set of spectra on the next 5 pages. Be sure to show your work on the spectra for full credit. Account for all numbered peaks in the IR. In peaks if necessary. Assign all NMR spectra as completely as possible: number of NMR signals, integration, chemical shift, and splitting the mass spectrum, determine degrees of unsaturation and label 4 IR Spectrum 3000 2000 1 1600 1200...
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,...
Please solve for each spectra and solve the final compound.
Problem 113 IR Spectrum 3000 1600 200 V (cm) Mass Spectrum UV Spectrum ma 238 nm (42) Amax 281 nm (2.7) M 150 solvent: methanol CH1oO2 40 80 120 160 200 240280 m/e 13C NMR Spectrum (1000 M ???, solution) 325 130.0 Dom DEPT H Gtt proton decoupled 325 1300 ppm 200 160 120 80 40 ? (ppm) H NMR Spectrum 400 MHz Coc, solution) 80 79 73 72ppm TMS...
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)
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