Draw a structure that is consistent with the MS, IR, and NMR spectra in Figures 1-3....
6. An unknown compound, CsH10O2, gives the NMR and IR shown below. Propose a structure. wavelength (m) 9 10 11 12 13 14 15 16 100 80 60 40 20 ol 4000 3500 3000 2500 1400 1200 1000 800 2000 1800 1600 wavenumber(cm) 600 SOHE 5.5.6 7.11 70 690 200 156 LA 1.6 10 8 (ppm)
Question 4 Consider the data provided in appendix B containing the mass spectrum, the IR spectrum and the 'H NMR of an unknown compound. Determine the structure of this compound base on the data provided. 100 117 M 80 60 abundance 40 20 0 10 20 30 40 50 60 70 100 110 120 130 140 150 160 80 90 ml 3 wavelength cm S 5.5 6 3.5 4.5 7 8 9 10 11 12 13 14 15 16 20...
Consider the data provided in appendix B containing the mass spectrum, the IR spectrum and the 'H NMR of an unknown compound. Determine the structure of this compound base on the data provided. (Make sure to show your work). 100 80 117 M 60 abundance 40 20 . = . 0 10 20 30 40 50 60 70 80 90 100 110 120 130' 140' 150 160 3.5 wavelength (um) 5.5 4.5 6 7 8 9 10 11 12 13...
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...
Question 4 Consider the data provided in appendix B containing the mass spectrum, the IR spectrum and the 'H NMR of an unknown compound. Determine the structure of this compound base on the data provided. (Make sure to show your work). Appendix B (question 4) 100 80 117 M 60 abundance 40 20 0 10 .. 60 20 30 40 50 70 80 90 100 110 120 130 140 150 160 3.5 4 4.5 wavelength (m) 5 5.5 6 8...
B. Determine the structure of and name the compound that gives rise to the following mass and IR spectra. 100 43 50 100 40 100 120 mlz waveiengin 3.5 4 4.5 5 5.5 6 7 8 9 10 11 12 13 14 15 16 100 80 800 2000 1800 1600 1400 1200 1000 2500 3000 3500 4000 wavenumber (cm
MAD ORG. CHEM. MIN. F2B Identify the functional groups present in each of the compounds below based on their IR spectra 100 80 60 CHyo A. 40 20 1600 1400 1200 800 1800 600 2000 1000 3000 2500 3500 80 60 40 20 0 4000 2500 800 600 1000 1400 1200 3000 2000 1800 1600 3500 80 60 C, 40 20 800 600 2500 1800 3500 4000 100 3000 2000 1600. 14m 1200 1000 80 60 D. 800 600 1200...
please help find the structure. thanks Unknown 11 – 1H-NMR Spectra 3.591 3.569 SOT 1.574 ISST -1.291 3.5 3.0 2.5 0 1. 0 .5 0.0 ppm Unknown 11 - 13C-NMR Spectrum - 220 200 180 160 140 120 100 80 0 ppm -62.80 ミュー 20 220 100 80 200 180 160 140 120 Unknown 11 - IR and Mass Spectra Unknown 11 - IR and was seven Reative itensity TTTTTTTH O- m 60 /z TRANSMITTANCE [%] لالالالالا OD 40'0o 3500...
q is for quadruplet and t is for triplet Compound A displays the following MS, 'HNMR, and IR spectra. Compound A decolorizes a solution of bromine in dichloromethane. Suggest a structure for Compound A consistent with all of the data given. Account for all of the numbered peaks in the MS, interpret each NMR signal, and identify each peak in the functional group region of the IR spectrum. 4. 100 80 20 10 30 50 60 70 100 A !...
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...