8 %Transmittance3462.983057.843022 511489 301443.831319.481155.121029.571008.82754.45693.07636 46w ece (CAMT-04 00)858075706560555045403530252015105--52000150010005003000250040003500Wavenumbers (cm-1)

IR Spectroscopy used to determine the functional group. IT measures the vibration of atoms and based…

Answered: %Transmittance 3462.98 3057.84 3022 51…

%Transmittance 3462.98 3057.84 3022 51 1489.30 1443.83 1319 48 1155.12 1029.57 1008.82 754.45 693.07 636 46 -5 4000 3500 3000 2500 2000 1500 1000 500

Fundamentals Of Analytical Chemistry

9th Edition

ISBN:9781285640686

Author:Skoog

Publisher:Skoog

Chapter25: Instruments For Optical Spectrometry

Section: Chapter Questions

Problem 25.20QAP

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Question

%Transmittance
3462.98
3057.84
3022 51
1489 30
1443.83
1319.48
1155.12
1029.57
1008.82
754.45
693.07
636 46
w ece (CAMT-04 00)
85
80
75
70
65
60
55
50
45
40
35
30
25
20
15
10
5-
-5
2000
1500
1000
500
3000
2500
4000
3500
Wavenumbers (cm-1)

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4000 3500 3000 2500 Wavenumbers (cm-1) 2000 20 1500 1000 500 1705.32 1354.36 1135.21 1476.83 997.91 2969.16 %Transmittance 1274.53 832.71 1427.75 953.40 553.28 790.43 1218.83 1585.98 894.05 671.73 780.29 463.73 100 C
You will check the outcome of reaction via infra-red spectroscopy: what are the diagnostic functional group peaks for the following compounds? You should also indicate the stretching motions responsible for absorbance. Dilantin benzil (unreacted starting material) Urea (unreacted starting material)
Lrdocaine USP (ATR) 95- 90 85 80 75 70 65 60 55 50 45 Lidocaine 40 4000 3500 3000 2500 2000 1500 1000 Wavenumbers (cm-1) %Transmittance IZ 3243.36 3021.30 2968.47 2921.13 2799.39 1661.66 1593.98 1491.43, 1449.061 422.12,384.681371.62 1291.03264.55 1206.99 1165.931119.56 1091.78072.77. 1034.33 970.79986.39 917.91, 885.23 763.76 703.94 615.01599.90
Transmittance (%) 100% 75% 50% 25% 0% 4000 3500 3000 OH 2500 2000 Spectrum 3B 1750 حسيمة 1500 Wavenumber (cm-¹) 1250 .OH 1000 OH 750 500
Please help me
OA B. OC D. CE. Compound G is an Aldehyde Compound H is a Carboxylic acid Compound is an alcohol A Compound B is a ketone Compound is an Adehyde A Compound B is a Ketone B Compound B is an Aldehyde Compound is a Ketone Compound is an Alcohol Compound B is a Carboxylic acid
6. C8H100 11 TRANSMITTANCE LOD HSP-04-492 0+ 10 4000 9 3000 8 5 7 6 : 5 ppm 2000 4 HAVENUMBERI-l 2: 2 1 3 1500 2 سهر 1 1000 0 500 200 T 180 CDS-06-431 DEPT-90 T 160 DEPT-135 140 120 100 لك -2 peaks u ppm 80 60 40 20 0
QUESTION 5 The IR, 'H NMR and 1°C NMR spectra of compound P are shown below. The molecular formula for compound P is CsH;NO2. Identify three (3) important absorption peaks on the IR spectrum and indicate the bond and wavenumber associated with each peak. Elucidate the structure of compound P and assign each peak in the 'H and 13C NMR spectra. (Hint: The compound consists of more than one functional group). а. b.
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3) Analyze the following IR spectra and match each spectrum to the correct molecule using the list of molecules (only one structure for each molecule; not all molecules will be used). Draw the correct molecule in the box to the right. Label the relevant peaks in the spectra with the proper functional group. If the absence of key peaks led to your choice, indicate which key peaks were absent. NH₂ OH OH OH HN
% TRANSMITTANCE 100 4000 3580 3.0 Proton NMA 2959.18 2938.83 3888 2.5 2874 38 1H 1H 230 220 210 200 190 PPM Carbon 13 NMA 2588 HAVENUMBERS ר 2.0 70 2888 60 1716.08. 1H 1.5 2 1460.30- 1377.35 - 1500 2H 1.5H SC SOTT 1024.33. 1000 843. 1.5H 1.0 PPM 20 10 PPM O MF C8H160 MW 128 %C 74.9 %H 12.6 0.5