structure of p-acetamidophenol
peak due to =CH sp2 carbon of arene is approx 3030 cm-1.
peak due to alcohal OH group frequency is nearly 3200 cm-1
peak due to C=O group bind to amine showing frequency nearly equal to 1650 cm-1
peak due to amide nitrogen N-H stretching is 3200-3500 cm-1 generally two peaks observed in this region.
2)- structure of phenacetin is and peak at 3269.20 and 3189.76 cm-1 is due to amide group (N-H) stretching of ring
peak from 2900-3000 cm-1 is due to the =CH of aromatic ring
peak at 1658.25 cm-1 and 1601.06 cm-1 is due to the C=O group of amide group.
peak at 1540.69 cm-1 is due to the ether group attatched to the ring.
Number 6 and 7. label both spectra of pure p-acetamidophenol and phenacetin product by indicating the...
Identify this compound (label all major functional groups on IR spectra). SAMPLE 100- % TRANSMITTANCE 4000 1000 3500 3000 2000 1500 2500 WAVENUMBERS 600.1
compare the IR spectra of the alcohol and product and comment on the completion of the reaction and purity of the product collected IR Spectra Alcohol lansmance 4000 3500 3000 1500 2500 2000 Wavenumbers (cm-1) 4000 3500 3000 2921.53 2500 Wavenumbers (cm-1) 2000 IR spectra product 1500 1444 44 1375 29 1000 1143.23 1039.81 916.32 797.83 423.62
IR Worksheet 1. For each spectrum below: 1) Label the major peaks with their approximate frequency. 2) Identify the bond vibration and possible functional group associated with each peak. 3) Match the spectra to one of these possible compounds: NH2 TRANSMITTANCE[%] pobo edo "2060 bo zdoo 160 Tobo 560 WAVENUMBER [cm-1] oot 08 TRANSMITTANCE [%] 09 01 02 4000 3500 3000 2500 2000 WAVENUMBER (cm-1] 1500 1000 500 οοο TRANSMITTANCE (6) οο οο οε 4000 3500 3000 1500 1000 2500...
Label IR spectra %Transmittance 4000 Methyl 3500 Salicylate 3191.67 3000 3154.07 3069.46 3025.59 2953.52 2500 Wavenumbers (cm-1) 2000 1675.04 1615 50 1577.90 1500 1487.02 1440.02 1327.21 1000 121441
Please label all important peaks on the IR Spectra. % Transmittance 4000 3500 3000 1500 1000 2500 2000 Wavenumbers (cm-1) Date: Thu Nov 07 13:57:45 2019 (GMT-05:0 Thu Nov 07 13:54:54 2019 (GMT-05:00) Scans: 32
Interpret the IR spectra for isoamyl acetate. Is the ester pure or crude? Label major bond types. 101, 100 %T 40+ 4000 3500 3000 2500 cm-1 2000 1500 1000 600
label functional groups responsible for each stretch if possible but most importantly label stretches %Transmittance 4000 100141 3500 3368.52 3000 3022960.78 2856.98 2500 Wavenumbers (cm-1) 2000 1603.46 1500 1494.05 1451.30 1383.94 1201.053 1057.56 974.1934.93 1000 845 60 777.88 731.30 695.32 591-32 525.50 512.49 507.12
Discuss the IR spectrum and what is the peak in IR that you can see for a specific functional group of the product? Discuss 1H NMR spectrum. Assign and interpret each peak. How do you determine the formation of the product using 1H NMR? IR Spectra 75 70 65 60 Transmittance 56 50 45 46 35 4000 3500 3000 1600 1000 2500 2000 Wenumbers (on 1) HNMR spectra Cheap
Draw the correct structure for C8H8 by analyzing the spectra below. Label the spectrum and explain your answer. 100 95 90 85 80 75 70 65 60 55 50 45 4000 3500 3000 2500 1500 1000 2000 500 Wavenumbers (cm-1) %Transmittance 2973.42 2940.13 2826.86 1469.79 1386.26 1363.07 1262.57 1020.89 850.92 724.39 459.11 4.5 3.5 3.0 4.0 2.5 2.0 0.5 ppm 1.5 1.0 00 3.04
On the provided spectra, do the following -Identify the peaks in the functional region of the spectra - Label the peak characteristics (strong, medium, weak, broad) - Identify the unknown molecule (butan-2-ol, cyclohexane, hexanal, cyclohexanone, tert-butylamine, propionic acid) 98 96 94 92 90 86 84 82 80 78 76 74 72 4000 3500 3000 2500 2000 1500 1000 Wavenumbers (cm-1) 98 96 94 92 90 86 84 82 80 78 76 74 72 4000 3500 3000 2500 2000 1500 1000...