C9H12
major IR peaks
2865 cm-1 corresponds to C-C stretch
3027 and 3062 lies in aromatic and C=C region
1455 cm-1 corresponds to CH3 bending
in molecular formula the no. of carbon and hydrogens are not in straight alkene form but it is aromatic .
mass spectrum shows the fragments of 120 as molecular ion peak , at 29 m/z peak of ethyl ion, 105 m/z 1-ethyl benzyl cation
the compound is 1-ethyl-2-methylbenzene or 2 -ethyl toluene.
C7H13Br
major IR peaks
2938 and 2849 cm-1 sharp
these peaks correspond to aliphatic C-H stretching
no peak suggest it having an alkene or aromatic ring
1445 cm-1 medium corresponds to CH2 bending
Mass Spectroscopic data
Molecular weight of C3H13Br = 176
no. of Carbons and Hydrogens in above aliphatic compound fit only when it is cyclic seven membered ring with onr Br substituent.
Instructions: Write the structure of each molecular formula using the IR and Mass Spec spectra. Important...
4. propose a reasonable structural solution to each problem. Waverurver (Chr-1) 132 150 104 103 77 3966 119 0 10 20 30 40 50 60 70 80 90 100 MIZ 110 120 130 140 150 160 170 180 -759 ---919 1000 --1304 1500 >1692 2000 2500 Wavenumber (cm-1) -2967 3–3068 3000 3500 Transmittance -759 ---919 1000 --1304 1500 >1692 2000 2500 Wavenumber (cm-1) -2967 3–3068 3000 3500 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...
Based on these three spectra, draw the compound. Which NMR signals are the most important, and how/what do they show? 100 BRUKER 90 80 70 Transmittance [%] 60 50 40 30 2872.78 1369.32 SY 3500 3000 2500 Wavenumber cm-1 1500 1000 500 M 108 Relative htensity 3 20 30 40 50 60 70 80 90 m/ 100 110 4658 -2.322
perpose a structure with a formula of C5H12O with the given information % Transmittance 0 4000 3500 3000 1500 1000 2500 2000 Wavenumber 1. Propose a structure for a compound with molecular formula C3H120 that exhibits the following 13C- NMR and IR spectra Carbon 13 NMR 73.8 100 90 80 70 60 50 40 Chemical shift (ppm) 30 20 10 0
Task to do: Carefully analyze the two IR spectra at the bottom, and identify one characteristic absorption peak for both the reactant and the product and record it in the following table. Compound Structure Functional group responsible for each peak IR Absorption peaks In cm name IR-1 110 00 90 80 70 - 60 40 30 20 4000 3500 3000 1000 2500 2000 100 Wweumbers (cm-1) IR-2 a00 2018 (GMT 06.00) 110 100 90- 70 60 50- 40 30 3500...
Use the spectra below to determine the molecular formula and chemical structure of the unknown compound. MASS 142 % of Base Peak 1147 40 50 70 80 5 100 % Transmittance Jari- 3000 1000 4000 'H NMR 300 MERE 2000 Wavenumber (cm) 3.0 25 20 15 Ppm 4.0 3.5 C/DEPT NMR 75.5 MHz ppm 60 50 40 80 70 90 100 110 120 170 160 150 140 130 ppm 4.5 4.0 3.5 3.0 2.5 2.0 1.5 ppm COSY 300 MHz...
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*')
Draw a structure that is consistent with the MS, IR, and NMR spectra in Figures 1-3. abundance اسلام سال M 73 10' 20' 30' 40'50' 60' 70' 80' 90 '100' 110' 120 130 140 150 160 m/z 25 3.5 4 4.5 wavelength (mm) 5 5.5 6 7 8 9 10 11 12 13 14 15 16 ECZO-EESZOW 4000 3500 3000 2500 1400 1200 1000 800 600 2000 1800 1600 wavenumber (cm) wavenumber (cm" 100 80 200 180 160 140 120...
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
For the graphs, people write the structure of this compound and explanation for analysis for each graphs. Molecular Formula: C9H12 Problem 3 - IR spectrum 100 80- 60- 40- 20- 3500 3000 2000 2500 1500 1000 Wavenumber (cm-1) -1027 -1095 1337 1378 -1455 -1602 1747 1801 1873 1941 2865 -3027 3062 Transmittance Problem 3 - H NMR spectrum (CDC13, 500 MHz) 3H 5H 2H 2H on the highlighted area to zoom. Click again to zoom back out. Problem 3 -...