Identify as many peaks as possible for each spectrum in the set you choose. Then determine...
Identify the peaks that identify the functional groups in the IR spectrum Unknown 4 C2H60 TRANSMITTANCE 1001- 0 900- 0 800- 0.700- 0.600- 0.500- 0.400- 0.300- 0200- 0.100- 0.000- 4000 IR Unknown 3500 3000 2500 2000 1000 1500 Load IR spectrum Load proton NMR Show structure Spectra are displayed using JSpecView Website maintained by Jennifer Muzyka Contact me at jennifer muzyka@centre edu. Unknown 5 C3H5NO TRANSMITTANCE 1.001 - 0.900- 0800- 0.700- 0.600- 0.500- 0.400- 0.300- 0 200- 0.100- 0 000...
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...
1) Identify the functional group (alkane, alkene, ketone, aldehyde, aldehyde, etc) for the compounds providing the IR spectra: % Transmittance 4000 3500 3000 1500 1000 500 2500 2000 Wavenumber(cm) % Transmittance 4000 3500 3000 1500 1000 500 2500 2000 Wavenumber(cm) % Transmittance 1000 3500 3000 1500 1000 500 2500 2000 Wavenumber (cm)
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
Identify the peaks that identify the functional groups in the IR spectrum Unknown 9 C4H604 TRANSMITGAN 1.001- 0 900- 0.800- 0.700- 0.600- 0.500- 0.400- 0 300- 0200- 0.100- 0.000-- - 4000 IR Unknown 2000 2500 3000 1500 1000 3500 Load IR spectrum Load proton NMR Show structure Spectra are displayed using Specview Website maintained by Mark Contact me at Jennifer muryka centre edu Unknown 21 C3H120 TRANSMIT GANCE 1.001- 0.900- 0 800- 0.700- 0.600- 0.500- 0.400 0.300- 0.200- 0.100- 0...
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...
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*')
Please evaluate the IR spectrum. Provide a structure and note any important peaks corresponding to the structure. It was an experiment using: isoamyl alcohol + acetic acid sulfuric acid as the catalyst and the products are isoamyl acetate and water. Thank you so much!!! 95 卜诒 卜” 90 85 寸 80 75 70 65 E 60 ー 55 50 45 40 35 30 25 20 4000 3500 3000 2500 2000 Wavenumbers (cm-1) 1500 1000 500 95 卜诒 卜” 90 85...
Click in the answer box to display choices Choose the compound that matches the IR spectrum shown. 100 50 4000 3500 3000 2500 2000 1500 1000 500 Wavenumber (cm-) A: D: The spectrum belongs to compound (select)
14.73 An unknown alcohol was treated with chromic acid to give a product with the following IR spectrum. Which of the following state- ments must be true? 100 % Transmittance 0 + 4000 3500 1500 1000 3000 2500 2000 Wavenumber (cm-") (a) The unknown compound must be a primary alcohol. (b) The unknown compound must be a secondary alcohol. (c) The unknown compound must be a tertiary alcohol. (d) The unknown compound must be acyclic.