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with formula C8H12O, label ir and NMR and propose a structure
question 7: C8H120 aabel all...
read the IR spectroscopy with detail please 119 100 %Transmittance 204 10 1600 1400 1200 1000000...
read the IR spectroscopy with detail please
119 100 %Transmittance 204 10 1600 1400 1200 1000000 600 3800 3600 3400 2400 2200 2000 1800 Wavenumbers (cm-1) 3000 2600 2600 3200 unknown % Transmittance 000 1200 1000 000 1600 1400 1800 2600 2800 3000 3200 2400 2200 2000 Wavenumbers (cm-1) 3600 3600 3400 We were unable to transcribe this image
Identify and Label all functional groups in the graph. Conduct an IR analysis. 80.0 70.0 60.0...
Identify and Label all functional groups in the graph. Conduct
an IR analysis.
80.0 70.0 60.0 50.0 40.0 30.0 20.0 10.0 an ” 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 Wavenumbers (cm-1
8) Propose a structure for the following compound based on its molecular formula (C4H2O2) and its...
8) Propose a structure for the following compound based on its molecular formula (C4H2O2) and its IR spectrum 25 2.6 2.7 2.8 2.9 3.5 4 45 9 10 11 12 13 14 15 16 4000 3800 36000 3400 3200 3000 2800 2600 2400 2200 2000 1400 1200 1000 1800 1600 Wavenumber(cm) 9) Propose a structure for the following compound based on its molecular formula (C6H120) and its IR spectrum wavelength (um) 25 26 2.7 2.8 2. 9 3 5 4...
Draw the expected IR for the following two molecules. Label each peak by functional group нал...
Draw the expected IR for the following two molecules. Label each peak by functional group нал 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000
C NMR data provided when possible, show part Determine the structure of CHO from the IR,...
C NMR data provided when possible, show part Determine the structure of CHO from the IR, NR and structures that correspond to individual NMR resonances 1800 1600 2000 1400 1200 1000 000 3600 3400 3200 3000 2800 2600 2400 2200 1.10 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0.0 normal decoupled 18C DEPT-135: (+) indicates positive peak (-) indicates negative peak indicates no peak DEPT-90 peaks indicated by Proposed Structure 200 180 160 140 120 100 80...
Draw the expected IR for the following two molecules. Label each peak by functional group (2.5...
Draw the expected IR for the following two molecules. Label each peak by functional group (2.5 points per spectra, 1.5 point for drawing spectra and, 1 point for labeling each peak) NH 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000
Draw the expected IR for the following two molecules. Label each peak by functional group (2.5...
Draw the expected IR for the following two molecules. Label each peak by functional group (2.5 points per spectra, 1.5 point for drawing spectra and, 1 point for labeling each peak) Он 1200 1000 1800 1400 3800 2800 2200 1600 3600 3400 3200 3000 3000 2800 2200 3600 3200 1800 3800 3400 1600 1400 1200 1000
Draw the expected IR for the following two molecules. Label each peak by functional group (7.5...
Draw the expected IR for the following two molecules. Label each peak by functional group (7.5 points per spectra, 3.5 points for drawing spectra and 4 points for labeling each peak) tha 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000
FRIDAY AND SATURDAY SECTIONS ONLY: Section: Uraw the expected IR for the following two molecules. Label...
FRIDAY AND SATURDAY SECTIONS ONLY: Section: Uraw the expected IR for the following two molecules. Label each peak by functional group (2.5 points per spectra, 1.5 point for drawing spectra and, 1 point for labeling each peak) 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000
8) Propose a structure for the compound with IR, NMR, and mass spectra shown below. The...
8) Propose a structure for the compound with IR, NMR, and mass spectra shown below. The integration of the peaks is in arbitrary units above them. 18 marks (Hint: check for possible isotopes in MS) 2400 2100 1800 1500 1200 900 600 300 OHz 12007 19554 J = 6.6 Hz 6667 5768 J = 6.6 Hz LLLLLLLLLL LLLLLLLLLLLLLLLLLLL Oppm (8) wavelength, micrometers 5 5.5 6 7 8 2.6 2.8 3 3.5 4 4.5 9 10 11 12 13 14 1516...
read the IR spectroscopy with detail please
119 100 %Transmittance 204 10 1600 1400 1200 1000000 600 3800 3600 3400 2400 2200 2000 1800 Wavenumbers (cm-1) 3000 2600 2600 3200 unknown % Transmittance 000 1200 1000 000 1600 1400 1800 2600 2800 3000 3200 2400 2200 2000 Wavenumbers (cm-1) 3600 3600 3400 We were unable to transcribe this image
Identify and Label all functional groups in the graph. Conduct
an IR analysis.
80.0 70.0 60.0 50.0 40.0 30.0 20.0 10.0 an ” 3800 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 800 Wavenumbers (cm-1
8) Propose a structure for the following compound based on its molecular formula (C4H2O2) and its IR spectrum 25 2.6 2.7 2.8 2.9 3.5 4 45 9 10 11 12 13 14 15 16 4000 3800 36000 3400 3200 3000 2800 2600 2400 2200 2000 1400 1200 1000 1800 1600 Wavenumber(cm) 9) Propose a structure for the following compound based on its molecular formula (C6H120) and its IR spectrum wavelength (um) 25 26 2.7 2.8 2. 9 3 5 4...
Draw the expected IR for the following two molecules. Label each peak by functional group нал 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000
C NMR data provided when possible, show part Determine the structure of CHO from the IR, NR and structures that correspond to individual NMR resonances 1800 1600 2000 1400 1200 1000 000 3600 3400 3200 3000 2800 2600 2400 2200 1.10 5.0 4.5 4.0 3.5 3.0 2.5 2.0 1.5 1.0 0.5 0.0 normal decoupled 18C DEPT-135: (+) indicates positive peak (-) indicates negative peak indicates no peak DEPT-90 peaks indicated by Proposed Structure 200 180 160 140 120 100 80...
Draw the expected IR for the following two molecules. Label each peak by functional group (2.5 points per spectra, 1.5 point for drawing spectra and, 1 point for labeling each peak) NH 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000
Draw the expected IR for the following two molecules. Label each peak by functional group (2.5 points per spectra, 1.5 point for drawing spectra and, 1 point for labeling each peak) Он 1200 1000 1800 1400 3800 2800 2200 1600 3600 3400 3200 3000 3000 2800 2200 3600 3200 1800 3800 3400 1600 1400 1200 1000
Draw the expected IR for the following two molecules. Label each peak by functional group (7.5 points per spectra, 3.5 points for drawing spectra and 4 points for labeling each peak) tha 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000
FRIDAY AND SATURDAY SECTIONS ONLY: Section: Uraw the expected IR for the following two molecules. Label each peak by functional group (2.5 points per spectra, 1.5 point for drawing spectra and, 1 point for labeling each peak) 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000 3800 3600 3400 3200 3000 2800 2200 1800 1600 1400 1200 1000
8) Propose a structure for the compound with IR, NMR, and mass spectra shown below. The integration of the peaks is in arbitrary units above them. 18 marks (Hint: check for possible isotopes in MS) 2400 2100 1800 1500 1200 900 600 300 OHz 12007 19554 J = 6.6 Hz 6667 5768 J = 6.6 Hz LLLLLLLLLL LLLLLLLLLLLLLLLLLLL Oppm (8) wavelength, micrometers 5 5.5 6 7 8 2.6 2.8 3 3.5 4 4.5 9 10 11 12 13 14 1516...
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