analyze the following IR spectrum
analyze the following IR spectrum 20 30 40 Transmittance [%] 50 60 70 80 90 8...
2) FT-IR spectrum of H Sal (1) 90 80 70 Transmittance [%] 60 50 용 15555 9992 8 1284.18 1029:57 = 858.07 750.01 3500 3000 1500 1000 500 2500 2000 Wavenumber cm-1 HO EN N- OH Assign the peaks with wavenumber from 1600 - 4000cm-1 (10 points) Wavenumber (cm-1) Intensity (s/m/w) Assignment ܒܢܰ CEN stretching C=C stretching Saturated C-H stretching Unsaturated =C-H stretching O-H stretching 3) FT-IR of H.Sal (2) 80 70 09 Transmittance [%] 50 40 30 20 IS...
pls interpret and analyze both IR Spectrum . thanks philip/johnson 105 100 95 90- 85 80 75 70 65 60 55 50- 45- 500 1000 1500 2000 2500 3500 3000 4000 Wavenumbers (om-1) %Transmittance 100 philipljphnson 95- 85 80 75 70- 65- 60 55 50 4000 3500 1000 500 3000 1500 2500 2000 %Transmittance 90 philip/johnson 105 100 95 90- 85 80 75 70 65 60 55 50- 45- 500 1000 1500 2000 2500 3500 3000 4000 Wavenumbers (om-1) %Transmittance...
please help me analyze the IR of these three compounds. The first one is M-nitrophenol, the second one is M-xylene, and the third one is toluene. m-Nitrophenol BRUKER 95 90 85 80 Transmittance [%] 75 70 65 60 1500 1000 3000 3500 2500 2000 Wavenumber cm-1 m-Xylene. 100 RUKER 90 80 70 Transmittance [%] 60 50 40 30 1500 1000 3500 3000 2500 2000 Wavenumber cm-1 Toluene བཟའགུལྡན Transmittance [%] 203040 50 60708090 100 ༢500 ༢000 3500 3000 2500 2000...
Identify the possible compound consistent with the following FT-IR spectrum. 100 80 60 Transmittance (6) 40 20 0 4000 3500 3000 1500 1000 500 2500 2000 Wave number,cm- Benceno benzaldehído etilbenceno O acetofenona O acetaldehído
What are the possible groups on both these IR spectras of ethyl trans-cinnamate? Module B - Session 5 (video 2 of 2) BRUKER 90 Transmittance [%] 70 80 60 50 IR Spectrum of Ethyl Trans-Cinnamate from Claisen Condensation 40 18. IST 58 883 ന ജഗ്ഗ് 1596.28 1455.20 1310.13 1201.61 450.70 3500 3000 1500 1000 500 2500 2000 Wavenumber cm-1 ID 48:47 / 49:03 HID Module B - Session 4 (video 1 of 2) BRUKER Press Esc to exit full screen...
Instructions: Write the structure of each molecular formula using the IR and Mass Spec spectra. Important that you justify with at least two arguments in each spectrum for which you present that structure. CH 3500 3000 1500 1000 2500 2000 Wavenumber(cm-1) 20 30 40 50 60 70 80 90 100 110 120 CHBr 100 Transmittance 3500 3000 2500 2000 Wavenumber(cm-1) 1500 1000 119 135 100 110 120 130 140 150 160 170 180 190 10 20 30 40 50 60...
identify the major peaks in the IR spectrum. Using proton NMR, suggest a possible structure. Transmittance [%] 50 60 70 20 30 40 80 90 100 RUKER 3500 3000 2977.06 2918.26 2867.68 2669.79 2549.41 2500 Wavenumber cm-1 2000 2036 1927.68 1810.92 1678.87 1611.81 1576.54 1515.82 1500 1000 1419.26 1321.41 1286.41 1183.30 1117.80 1041.01 1021.43 961.88 948.77 840.08 755.70 688.27 608.01 O PP
Assign the peak for both of the IR spectrum below and identify what compound is this and draw the structure of the compound. 100 90 80 70 W 60 50 % Transmission 40 30 - 923 1677 1285 20 - 702 10 0 4000 3500 3000 2500 2000 1500 1000 Wavenumber (cm) 100 80 m % Transmission 1660 1209 1438 886 757 0 4000 3500 3000 2500 1500 1000 2000 Wavenumber (cm*')
which alcohol is being shown by the spectra 60 Transmittance [%] 70 80 90 100 RUKER 3500 3328,20 3000 2929.49 2861.33 2500 Wavenumber cm-1 2000 1500 1465.75 - 1053.70 1000 728.47 500 proton.kp CDC13 C:\opt\Bruker\TOPSPIN) Organic2 61 3.593 2.261 -1.544 — 1.309 -0.885 - — 1.6 1.4 ppm Create PDF files without this message by purchasing novaPDF printer (http://www.novapdf.com) ppm 1.0 0.9 ppm 3.5 3.0 2.5 ppm 192 1.00
please analyze this spectrum stating the functional groups present and their corresponding wavenumbers and band strength 100 BRUKER 06 80 70 Transmittance [%] 09 50 IR Spectrum of Ethyl Trans- Cinnamate from Wittig Reaction 40 கக்ககம் SO88888888949889878888888 B&&&& 3500 3000 1500 1000 500 2500 2000 JALNumborem.