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1. Formula C,H4O 4000 3500 2H 3H 3H 2H 2H 2H 1.5 2.0 4.5 3.5 3.0 2.5 1.0 PPM 4.0 20es 0*250 T6 61 '8201 LSIT 60...
5.0 69 4.5 68 3.5 3.0 $ 2.5 2.0 67 65 64 63 61 1.0 0.5...
5.0 69 4.5 68 3.5 3.0 $ 2.5 2.0 67 65 64 63 61 1.0 0.5 3.0 3.5 4.0 4.5 5.0 5.5 6.0 6.5 7.0 UNEMPLOYMENT RATE (Percent)
Draw the structures of the Compounds 2.0 3.64 Unsat. Index = (2C+2-H-X +N)/2 = 1.5 1.06...
Draw the structures of the Compounds
2.0 3.64 Unsat. Index = (2C+2-H-X +N)/2 = 1.5 1.06 6.86 7.00 d = 2.44 ppm, Compound 18a. C, H, N quartet, 2H 1.0 7.02 6.84 2.43 2.45 1.08 1.04 a = 7.01 ppm, c = 3.64 ppm, b = 6.85 ppm, 0.5 doublet, 2H doublet, 2H singlet, 2H e = 1.06 ppm, 2.41 2.47 triplet, 3H 8, ppm 0.0 8.0 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 20 1.5...
please help! c 3.86 ppm, singlet, 3H d-2.52 ppm, singlet, 3H Compound A: CoH1002 TSI a...
please help!
c 3.86 ppm, singlet, 3H d-2.52 ppm, singlet, 3H Compound A: CoH1002 TSI a 7.89 ppm, doublet, 2H b-7.89 ppm, doublet, 2H Unsat. Index- (2C+2-H-X+N)/2 8, ppm 9.0 7.0 60 3.0 2.0 ? 3, 5-dimethylbenzaldehyde, NaOH, H2O, heat h 2.31 ppm, singlet, 6H 3-1 a #8 ppm, doublet, 2H b-7.60 ppm, doublet, 1H c- 7.33 ppm, singlet, 2H Compound B: C1H1O2 g-3.86 ppm, singlet, 3H d-7.28 ppm, doublet, 1 H e 6.99 ppm, singlet, 1H C f 6.98...
Please help me find the unknown structure, Thanks. Unknown 261H-NMR Spectra 3.3 ppm 4-0 4.5 4.0...
Please help me find the unknown structure, Thanks.
Unknown 261H-NMR Spectra 3.3 ppm 4-0 4.5 4.0 3.5 3.4 2.5 2.0 .0 .s a. 3.00 Unknown 26 - 13C-NMR Spectrum 32 34 28 24 20 14 ppm 60 40 200 180 160 140 120 100 20 Unknown 26 IR and Mass Spectra 100 80 40 20 50 75 100 125 m/z 2500 WAVENUMBER [cm-1] 1500 3500 2000 1000 4000 3000 500 TRANSMITTANCE %] Raufive hitensity 06 7 Unknown 26 1H-NMR Spectra...
Consider the cyclohexanol/cyclohexene mixture spectrum. Calculate the observed cyclohexanol/cylcohexene ratio. Spectrum C cyclohexene & cyclohexanol mixture solvent: CDCl 3.0 2.5 5.5 5.0 4.5 4.0...
Consider the cyclohexanol/cyclohexene mixture spectrum.
Calculate the observed cyclohexanol/cylcohexene ratio.
Spectrum C cyclohexene & cyclohexanol mixture solvent: CDCl 3.0 2.5 5.5 5.0 4.5 4.0 3.5 2.0 1.5 1.0 0.5 ppm
Spectrum C cyclohexene & cyclohexanol mixture solvent: CDCl 3.0 2.5 5.5 5.0 4.5 4.0 3.5 2.0 1.5 1.0 0.5 ppm
Solve and label the HNMR and CNMR Unknown #2 CgH180 3.5 3.0 2.5 2.0 1.5 1.0...
Solve and label the HNMR and CNMR
Unknown #2 CgH180 3.5 3.0 2.5 2.0 1.5 1.0 f1 (ppm) 0 4 3 2 0 f1 (ppm)
hnmr spectroscopy Analyze the spectrums and determine the structures Please help. I’m really confused with how...
hnmr spectroscopy
Analyze the spectrums and determine the structures
Please help. I’m really confused with how some of the
structures might be.
2) C,HuO 3H fer 4H 0.8 PPM 0. 1.0 1.4 1.2 2.2 1.0 1. 2.0 2.8 2.4 2.0 40 z00a 4000 3000 252e 1500 1720 2202 4) CHo 6H 1H Methylee protos adjacent to chiral centers may not be 1H 1H equlvalent 1.0 PPM 3.0 2.0 0.5 3:5 2.5 1.5 42 28 158e 4000 3500 2500 200 C-...
NMR & IR post lab question help! NMR and IR 4.5 4.0 3.5 3.0 2.5 2.0...
NMR & IR post lab question help!
NMR and IR 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppm IH The 'H NMR for the unknown C: 20 7.5 7.0 6.5 6.0 6.5 5.0 4.5 4.0 3.5 3.0 25 20 519 05 Proton peak Integration Chemical Shift (ppm) Neighbors (m) Splitting pattern (+1) report as singlet/doublettripletlets. C must be an aliphatic alcohol. There is a strong O-H stretch in the IR and zero degrees of unsaturation. The remaining structure...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of each compound (4 points) (30 points total) 2.0 3.64 Unsat. Index = (2C + 2-H-X +N)/2 = 1.5 1.06 6.86 7.00 d = 2.44 ppm, Compound 18a. C,H, N 1.0 7.02 6.84 quartet, 2H 2.43 2.45 1.08 1.04 a = 7.01 ppm, b = 6.85 ppm, c = 3.64 ppm, 0.5 doublet, 2H doublet,...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of each compound (4 points) (30 points total) 2.0 3.64 Unsat. Index = (2C+2-H-X +N)/2 = 1.5 1.06 6.86 7.00 d = 2.44 ppm, Compound 18a. C10H,,N quartet, 2H 1.0 7.02 6.84 2.43 2.45 c = 3.64 ppm, 1.08 1.04 a = 7.01 ppm, b = 6.85 ppm, doublet, 2H doublet, 2H singlet, 2H 0.5...
5.0 69 4.5 68 3.5 3.0 $ 2.5 2.0 67 65 64 63 61 1.0 0.5 3.0 3.5 4.0 4.5 5.0 5.5 6.0 6.5 7.0 UNEMPLOYMENT RATE (Percent)
Draw the structures of the Compounds
2.0 3.64 Unsat. Index = (2C+2-H-X +N)/2 = 1.5 1.06 6.86 7.00 d = 2.44 ppm, Compound 18a. C, H, N quartet, 2H 1.0 7.02 6.84 2.43 2.45 1.08 1.04 a = 7.01 ppm, c = 3.64 ppm, b = 6.85 ppm, 0.5 doublet, 2H doublet, 2H singlet, 2H e = 1.06 ppm, 2.41 2.47 triplet, 3H 8, ppm 0.0 8.0 7.5 7.0 6.5 6.0 5.5 5.0 4.5 4.0 3.5 3.0 2.5 20 1.5...
please help!
c 3.86 ppm, singlet, 3H d-2.52 ppm, singlet, 3H Compound A: CoH1002 TSI a 7.89 ppm, doublet, 2H b-7.89 ppm, doublet, 2H Unsat. Index- (2C+2-H-X+N)/2 8, ppm 9.0 7.0 60 3.0 2.0 ? 3, 5-dimethylbenzaldehyde, NaOH, H2O, heat h 2.31 ppm, singlet, 6H 3-1 a #8 ppm, doublet, 2H b-7.60 ppm, doublet, 1H c- 7.33 ppm, singlet, 2H Compound B: C1H1O2 g-3.86 ppm, singlet, 3H d-7.28 ppm, doublet, 1 H e 6.99 ppm, singlet, 1H C f 6.98...
Please help me find the unknown structure, Thanks.
Unknown 261H-NMR Spectra 3.3 ppm 4-0 4.5 4.0 3.5 3.4 2.5 2.0 .0 .s a. 3.00 Unknown 26 - 13C-NMR Spectrum 32 34 28 24 20 14 ppm 60 40 200 180 160 140 120 100 20 Unknown 26 IR and Mass Spectra 100 80 40 20 50 75 100 125 m/z 2500 WAVENUMBER [cm-1] 1500 3500 2000 1000 4000 3000 500 TRANSMITTANCE %] Raufive hitensity 06 7 Unknown 26 1H-NMR Spectra...
Consider the cyclohexanol/cyclohexene mixture spectrum.
Calculate the observed cyclohexanol/cylcohexene ratio.
Spectrum C cyclohexene & cyclohexanol mixture solvent: CDCl 3.0 2.5 5.5 5.0 4.5 4.0 3.5 2.0 1.5 1.0 0.5 ppm
Spectrum C cyclohexene & cyclohexanol mixture solvent: CDCl 3.0 2.5 5.5 5.0 4.5 4.0 3.5 2.0 1.5 1.0 0.5 ppm
Solve and label the HNMR and CNMR
Unknown #2 CgH180 3.5 3.0 2.5 2.0 1.5 1.0 f1 (ppm) 0 4 3 2 0 f1 (ppm)
hnmr spectroscopy
Analyze the spectrums and determine the structures
Please help. I’m really confused with how some of the
structures might be.
2) C,HuO 3H fer 4H 0.8 PPM 0. 1.0 1.4 1.2 2.2 1.0 1. 2.0 2.8 2.4 2.0 40 z00a 4000 3000 252e 1500 1720 2202 4) CHo 6H 1H Methylee protos adjacent to chiral centers may not be 1H 1H equlvalent 1.0 PPM 3.0 2.0 0.5 3:5 2.5 1.5 42 28 158e 4000 3500 2500 200 C-...
NMR & IR post lab question help!
NMR and IR 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppm IH The 'H NMR for the unknown C: 20 7.5 7.0 6.5 6.0 6.5 5.0 4.5 4.0 3.5 3.0 25 20 519 05 Proton peak Integration Chemical Shift (ppm) Neighbors (m) Splitting pattern (+1) report as singlet/doublettripletlets. C must be an aliphatic alcohol. There is a strong O-H stretch in the IR and zero degrees of unsaturation. The remaining structure...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of each compound (4 points) (30 points total) 2.0 3.64 Unsat. Index = (2C + 2-H-X +N)/2 = 1.5 1.06 6.86 7.00 d = 2.44 ppm, Compound 18a. C,H, N 1.0 7.02 6.84 quartet, 2H 2.43 2.45 1.08 1.04 a = 7.01 ppm, b = 6.85 ppm, c = 3.64 ppm, 0.5 doublet, 2H doublet,...
18. Draw the structures of Compound 18a. and 18b. (18 pts), clearly indicate your assignments of all proton resonances (8 pts). Calculate the Unsaturation Index of each compound (4 points) (30 points total) 2.0 3.64 Unsat. Index = (2C+2-H-X +N)/2 = 1.5 1.06 6.86 7.00 d = 2.44 ppm, Compound 18a. C10H,,N quartet, 2H 1.0 7.02 6.84 2.43 2.45 c = 3.64 ppm, 1.08 1.04 a = 7.01 ppm, b = 6.85 ppm, doublet, 2H doublet, 2H singlet, 2H 0.5...
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