label the IR with the bonds. MW 3600 3200 2800 2400 2000 1800 1600 1400 1200...
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
2. The following IR spectra each include the structure of the corresponding compound directly on the spectrum (continued on following pages). • Based on the given structures and the information provided in Tables 8.1 and 8.2, assign as many of the major absorptions as possible directly on the spectra o indicating what type of bond O and whether it corresponds to bending or a stretching vibration. Transmittance (%) 0 + 4000 3600 3200 2000 2400 1400 1200 1000 800 600...
Deduce the structure please Molecular Formula - CgH120 국 3600 3400 3200 3000 2800 2600 2400 2200 2000 1800 1600 1400 1200 1000 7 6 5 4 3 2 1
4) Unknown 428 (29.30% C,5.74% H) 4000 3600 3200 2800 2400 2000 1800 1800 1400 1200 1000 300 600 100- Relative Intensity 10 20 30 40 50 60 80 90 100 110 120 70 m/z peo ppm 10 ppm Chemical Formula: Degrees of Unsaturation: Label Absorbance Max Relative Intensity Shape Functional group/hybridization Considerations, Comments Signal Label Shift Integration Multiplicity Adjacent protons Hydrogen type Considerations, Comments Molecular Ion mass Special Considerations, Comments (e.g. nitrogen, bromine, or chlorine present?) #4 Final Answer:
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
IR Worksheet-CHEM 2460 Spectrum A- Fare the IR spectra of the compounds shown, In Spectrum A-F, assign the major absorptions above 1500 em in the spectrum of each compound, (using and 8 2 [see background informationD) A. IR spectra of phenylethyne 100 80 40 20- 4000 3600 3200 2800 2400 2000 1800 1600 1400 1200 1000800 Wavenumber (cm) IR spectra of n-butyl acetate 100 B. 80 60 40 CHsCO(CH2)30% 20 4000 3600 3200 2800 2400 2000 1800 1600 1400 1200...
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
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
Spectrum A - Fare the IR spectra of the compounds showna. In Spectrum A -F. assign the major absorptions above .-1500 cm. in the spectrum of each compo and, (using Tables and 8 2 Isee background information). section C. IR spectra of N.N-dimethylacetamide 100 60 40 CH CN(CHsh 20 0-T 4000 3000 3200 2000 2400 2000 1 1600 1400 1200罒… Waverumtor (cmr*) D. IR spectra of diethyl ether (Also assign the peak at 1 1 10 cm-1) 100 80 60...