show me how to get the answer with the pieces from nmr and ir please
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show me how to get the answer with the pieces from nmr and ir please o n son mol th : 0.00100o C. m! +0. elow mol ED...
Find the compounds using IR and NMR: Problem 25 2251 IR Spectrum (liquid film) 800 1600...
Find the compounds using IR and NMR:
Problem 25 2251 IR Spectrum (liquid film) 800 1600 1200 4000 3000 2000 v (cm) 100 Mass Spectrum M 117 80 77 60 91 40 20 CgH7N 200 80 120 160 240 280 40 m/e expansion 13C NMR Spectrum (100.0 MHz, CDCI, solution) 130 129 ppm DEPT CH Cн,! сн! expansion 130 129 ppm solvent proton decoupled (ppm) 40 200 160 120 80 H NMR Spectrum (400 MHz. CDCI, solution) TMS 10 7...
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,...
Fall 2019 Problem 3 IR Spectrum (CHC solution) 1350 1170 4000 3000 800 2000 v (cm)...
Fall 2019 Problem 3 IR Spectrum (CHC solution) 1350 1170 4000 3000 800 2000 v (cm) 1600 1200 100 Mass Spectrum 91 80 M 200 60 155 40 172 20 Cg H1203S 240 280 200 120 m/e 160 80 40 13C NMR Spectrum (20.0 MHz, CDCI, solution) C-H C-H H-GH -CH -CH solvent TMS proton decoupled 0 8(ppm) 40 80 120 160 200 H NMR Spectrum (100 MHz. CDCI, solution) TMS 1 8 (ppm) 6 7 8 yeed % of...
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,...
Attached are four spectra for isomer with the MF= c12h14o4. Determine the structure for each molecule...
Attached are four spectra for isomer with the MF=
c12h14o4. Determine the structure for each molecule and draw them
below.
problem 63 IR Spectrum (CCI, solution) 1765 4000 3000 1200 800 2000 V (cm ) Mass Spectrum UV Spectrum & 8 8 g 8 of base 2 mar 269 nm (10910€ 2.7) humax 263 nm (10910 2.7) M -222 (< 1) 169 sahent: methanol 8 C12H1404 240 280 40 80 120 160 200 13C NMR Spectrum (50.0 MHz, COCI, solution)...
Deduce the structure based on the information below: Concepts: organic spectroscopy, organic chemistry Problem 69 2288...
Deduce the structure based on the information below:
Concepts: organic spectroscopy, organic chemistry
Problem 69 2288 IR Spectrum (liquid film) 4000 3000 1200 800 2000 V (cm 1600 ) Mass Spectrum 88 TTTTTTTTTTT % of base poak No significant UV absorption above 220 nm M+ = 94 < 1%) 40 80 160 200 240 280 120 m/ 13C NMR Spectrum (20.0 MHz, CDCI, solution) TMS solvent prolon decoupled 200 160120 80 40 0 8 (ppm) 1H NMR Spectrum (100 MHz,...
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...
Fall 2019 Problem 5 IR Spectrum (iquid fim) 1715 4000 3000 2000 V (cm) 1600 1200...
Fall 2019 Problem 5 IR Spectrum (iquid fim) 1715 4000 3000 2000 V (cm) 1600 1200 800 100 44 Mass Spectrum 80 60 58 20 M. 86 C5H100 280 40 240 80 200 120 160 13C NMR Spectrum (20.0 MHz, CDCI, solution) -CH3 C-H proton decoupled TMS CH solvent ul 5 (ppm) 40 80 120 160 200 H NMR Spectrum (100 MHz, CDC, solution) expansion of 400 MHz spectrum 20 Hz TMS 0.99 ppm 2.21 2.31 9.75 2 3 6...
do the spec problem Problem 9 IR Spectrum (kuid im) 0.0 800 1600 1200 2000 V (cm) 3000 4000 Mass Spectrum 0.5F 100 8...
do the spec problem
Problem 9 IR Spectrum (kuid im) 0.0 800 1600 1200 2000 V (cm) 3000 4000 Mass Spectrum 0.5F 100 80 60 UV spectrum 1,0 77 107 5.815 mg/ 10 mls path length: 1.00 cm solvent: ethanel M 122 20E 1.5 300 350 250 200 200 280 240 120 160 40 80 (nm) m/e 13C NMR Spectrum Aath (20.0 MHz, CDCI, solution) expansion x5 off-resonance decoupled proton decoupled 200 160 120 80 8 (ppm) 40 0 1H...
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,...
Find the compounds using IR and NMR:
Problem 25 2251 IR Spectrum (liquid film) 800 1600 1200 4000 3000 2000 v (cm) 100 Mass Spectrum M 117 80 77 60 91 40 20 CgH7N 200 80 120 160 240 280 40 m/e expansion 13C NMR Spectrum (100.0 MHz, CDCI, solution) 130 129 ppm DEPT CH Cн,! сн! expansion 130 129 ppm solvent proton decoupled (ppm) 40 200 160 120 80 H NMR Spectrum (400 MHz. CDCI, solution) TMS 10 7...
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,...
Fall 2019 Problem 3 IR Spectrum (CHC solution) 1350 1170 4000 3000 800 2000 v (cm) 1600 1200 100 Mass Spectrum 91 80 M 200 60 155 40 172 20 Cg H1203S 240 280 200 120 m/e 160 80 40 13C NMR Spectrum (20.0 MHz, CDCI, solution) C-H C-H H-GH -CH -CH solvent TMS proton decoupled 0 8(ppm) 40 80 120 160 200 H NMR Spectrum (100 MHz. CDCI, solution) TMS 1 8 (ppm) 6 7 8 yeed % of...
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,...
Attached are four spectra for isomer with the MF=
c12h14o4. Determine the structure for each molecule and draw them
below.
problem 63 IR Spectrum (CCI, solution) 1765 4000 3000 1200 800 2000 V (cm ) Mass Spectrum UV Spectrum & 8 8 g 8 of base 2 mar 269 nm (10910€ 2.7) humax 263 nm (10910 2.7) M -222 (< 1) 169 sahent: methanol 8 C12H1404 240 280 40 80 120 160 200 13C NMR Spectrum (50.0 MHz, COCI, solution)...
Deduce the structure based on the information below:
Concepts: organic spectroscopy, organic chemistry
Problem 69 2288 IR Spectrum (liquid film) 4000 3000 1200 800 2000 V (cm 1600 ) Mass Spectrum 88 TTTTTTTTTTT % of base poak No significant UV absorption above 220 nm M+ = 94 < 1%) 40 80 160 200 240 280 120 m/ 13C NMR Spectrum (20.0 MHz, CDCI, solution) TMS solvent prolon decoupled 200 160120 80 40 0 8 (ppm) 1H NMR Spectrum (100 MHz,...
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...
Fall 2019 Problem 5 IR Spectrum (iquid fim) 1715 4000 3000 2000 V (cm) 1600 1200 800 100 44 Mass Spectrum 80 60 58 20 M. 86 C5H100 280 40 240 80 200 120 160 13C NMR Spectrum (20.0 MHz, CDCI, solution) -CH3 C-H proton decoupled TMS CH solvent ul 5 (ppm) 40 80 120 160 200 H NMR Spectrum (100 MHz, CDC, solution) expansion of 400 MHz spectrum 20 Hz TMS 0.99 ppm 2.21 2.31 9.75 2 3 6...
do the spec problem
Problem 9 IR Spectrum (kuid im) 0.0 800 1600 1200 2000 V (cm) 3000 4000 Mass Spectrum 0.5F 100 80 60 UV spectrum 1,0 77 107 5.815 mg/ 10 mls path length: 1.00 cm solvent: ethanel M 122 20E 1.5 300 350 250 200 200 280 240 120 160 40 80 (nm) m/e 13C NMR Spectrum Aath (20.0 MHz, CDCI, solution) expansion x5 off-resonance decoupled proton decoupled 200 160 120 80 8 (ppm) 40 0 1H...
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,...
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