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Amswer all parts please QUICKLY 6. Use the spectral data given to identify the structure of the unknown compound wit...
Name: 6. Use the spectral data given to identify the structure of the unknown compound with...
Name: 6. Use the spectral data given to identify the structure of the unknown compound with chemical formula (C12H1602). (20 points) UV Spectum: 2 = 240 nm MW = 192 g/mol, IR resonance: 1610, 1729 cm, 13C NMR Spectrum (1000 MHZ COCI, solution DEPT CHA CHA CH prolon de coupled 200 160 120 08 (ppm) TH NMR Spectrum (400 M2. CDCI, tion) person folhas Ab 2 BC 75 PPM ܢܐ & TMS 109 7 5 8 (ppm)
) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure...
) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure for this compound in the box at the bottom of the page. Peak assignments written on the spectra may be worth partial credit. (5 marks) r IR Spectrum liquid film) 1735 1717 4000 3000 1200 800 2000 1600 V (cm) 13C NMR Spectrum (100 MHz, CDCI, solution) DEPT CHI Chit Cht solvent proton decoupled 100 no Sloml proton decoupled 200 160 120 80 40...
Use the spectral data provided to determine the structure of the following organic conpounds. IR Spectrum...
Use the spectral data provided to determine the structure of
the following organic conpounds.
IR Spectrum ouid im) 3410 4000 3000 2000 1600 1200 V (om: 800 100 Mass Spectrum 43 80 60 M (15) 71 20 40 120 80 160 200 240 280 m/e 13C NMR Spectrum (50.0 M, COCI, solution) DEPT CHt CH,t CHt solvent proton decoupled 0 8 (ppm) 40 80 120 200 160 'H NMR Spectrum (200 MHz, CDCI, solution) expansion exchanges with Dy0 50 pom...
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,...
Find the structure IR Spectrum quid 4000 3000 2000 V (cm 1600 ) 1200 800 0.0...
Find the structure
IR Spectrum quid 4000 3000 2000 V (cm 1600 ) 1200 800 0.0 Mass Spectrum 0.5t of base peak UV spectrum 1.075 mg/10ms path length: 0.10 cm solvent: ethanol CH100 280 1.5 40 80 120 160 m/e 200 240 200 250 cm 300 13C NMR Spectrum (1250 MHZ COCI, solution) DEPT CH CH CH! proton decoupled 200160120 80 40 08 (ppm) TH NMR Spectrum (600 MHz, CDCI, solution) expansions expansion pom 10 9 8 7 6 5...
Fill out the table below given the information (please explain) Problem 6 IR Spectrum liquid film)...
Fill out the table below given the information (please
explain)
Problem 6 IR Spectrum liquid film) 1716 4000 3000 1200 800 2000 V (cm 1600 ) Mass Spectrum UV Spectrum A max 289 nm (log10€ 1.4) of base peak solvent methanol M. 86 40 80 120 160 200 240 280 m / 13C NMR Spectrum (100 MHz, CDCI, solution) DEPT CHI CH.CH proton decoupled solvent 200 160 120 80 400 8 (ppm) 'H NMR Spectrum (200 MHz, COCI, solution) 10...
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
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,...
Based on the following spectroscopic data of an unknown compound with molecular formula C8H6S, (i) determine...
Based on the following
spectroscopic data of an unknown compound with molecular formula
C8H6S, (i) determine the chemical structure of this compound; (ii)
assign all the signals in the 1H-NMR spectrum & 13C-NMR
spectrum. NMR is complete
۳۳-۳-rr-T-------- IR Spectrum (KBr disc) 4000 3000 1200 800 2000 1600 V (cm) M ** = 13 Mass Spectrum بالليليللليلعليا % of base peak CgHES 40 80 200 240 280 120 m 160 /e 13C NMR Spectrum (100.0 MHz, CDCI, solution) expansion DEPT...
Identify the structure Problem 120 mm IR Spectrum liquid film) 1734 4000 3000 2000 1200 800...
Identify the structure
Problem 120 mm IR Spectrum liquid film) 1734 4000 3000 2000 1200 800 1600 V (cm) 100 Mass Spectrum M 128 80 60 40F wodowe No significant UV absorption above 220 mm 83 100 113 C-H1202 40 80 120 200 240 280 160 m/e 13C NMR Spectrum (100.0 MHZ. CDCI, solution) DEPT Chat Chat Cht W proton decoupled 200 160 120 80 40 O 8 (ppm) H NMR Spectrum (400 MHE, COCI, solution) expansions oppm 1936 ppi...
Name: 6. Use the spectral data given to identify the structure of the unknown compound with chemical formula (C12H1602). (20 points) UV Spectum: 2 = 240 nm MW = 192 g/mol, IR resonance: 1610, 1729 cm, 13C NMR Spectrum (1000 MHZ COCI, solution DEPT CHA CHA CH prolon de coupled 200 160 120 08 (ppm) TH NMR Spectrum (400 M2. CDCI, tion) person folhas Ab 2 BC 75 PPM ܢܐ & TMS 109 7 5 8 (ppm)
) A compound with molecular formula CxH 1403 displays the following spectral data. Propose a structure for this compound in the box at the bottom of the page. Peak assignments written on the spectra may be worth partial credit. (5 marks) r IR Spectrum liquid film) 1735 1717 4000 3000 1200 800 2000 1600 V (cm) 13C NMR Spectrum (100 MHz, CDCI, solution) DEPT CHI Chit Cht solvent proton decoupled 100 no Sloml proton decoupled 200 160 120 80 40...
Use the spectral data provided to determine the structure of
the following organic conpounds.
IR Spectrum ouid im) 3410 4000 3000 2000 1600 1200 V (om: 800 100 Mass Spectrum 43 80 60 M (15) 71 20 40 120 80 160 200 240 280 m/e 13C NMR Spectrum (50.0 M, COCI, solution) DEPT CHt CH,t CHt solvent proton decoupled 0 8 (ppm) 40 80 120 200 160 'H NMR Spectrum (200 MHz, CDCI, solution) expansion exchanges with Dy0 50 pom...
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,...
Find the structure
IR Spectrum quid 4000 3000 2000 V (cm 1600 ) 1200 800 0.0 Mass Spectrum 0.5t of base peak UV spectrum 1.075 mg/10ms path length: 0.10 cm solvent: ethanol CH100 280 1.5 40 80 120 160 m/e 200 240 200 250 cm 300 13C NMR Spectrum (1250 MHZ COCI, solution) DEPT CH CH CH! proton decoupled 200160120 80 40 08 (ppm) TH NMR Spectrum (600 MHz, CDCI, solution) expansions expansion pom 10 9 8 7 6 5...
Fill out the table below given the information (please
explain)
Problem 6 IR Spectrum liquid film) 1716 4000 3000 1200 800 2000 V (cm 1600 ) Mass Spectrum UV Spectrum A max 289 nm (log10€ 1.4) of base peak solvent methanol M. 86 40 80 120 160 200 240 280 m / 13C NMR Spectrum (100 MHz, CDCI, solution) DEPT CHI CH.CH proton decoupled solvent 200 160 120 80 400 8 (ppm) 'H NMR Spectrum (200 MHz, COCI, solution) 10...
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
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,...
Based on the following
spectroscopic data of an unknown compound with molecular formula
C8H6S, (i) determine the chemical structure of this compound; (ii)
assign all the signals in the 1H-NMR spectrum & 13C-NMR
spectrum. NMR is complete
۳۳-۳-rr-T-------- IR Spectrum (KBr disc) 4000 3000 1200 800 2000 1600 V (cm) M ** = 13 Mass Spectrum بالليليللليلعليا % of base peak CgHES 40 80 200 240 280 120 m 160 /e 13C NMR Spectrum (100.0 MHz, CDCI, solution) expansion DEPT...
Identify the structure
Problem 120 mm IR Spectrum liquid film) 1734 4000 3000 2000 1200 800 1600 V (cm) 100 Mass Spectrum M 128 80 60 40F wodowe No significant UV absorption above 220 mm 83 100 113 C-H1202 40 80 120 200 240 280 160 m/e 13C NMR Spectrum (100.0 MHZ. CDCI, solution) DEPT Chat Chat Cht W proton decoupled 200 160 120 80 40 O 8 (ppm) H NMR Spectrum (400 MHE, COCI, solution) expansions oppm 1936 ppi...
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