Attached 1st Reaction was performed in the Synthesis of Dihydrosafrole via Friedel-Crafts Acylation & Reduction Experiment resulting in following IR spectra. Can you analyze it and fill the following table? Are their any impurities found? Peak Position cm-1 Bond Type Functional Group
Attached 1st Reaction was performed in the Synthesis of Dihydrosafrole via Friedel-Crafts Acylation & Reduction Experiment resulting in following IR spectra. Can you analyze it and fill the following table? Are their any impurities found? Peak Position cm-1 Bond Type Functional Group
Principles of Instrumental Analysis
7th Edition
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Chapter6: An Introduction To Spectrometric Methods
Section: Chapter Questions
Problem 6.1QAP
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Question
Attached 1st Reaction was performed in the Synthesis of Dihydrosafrole via Friedel-Crafts Acylation & Reduction Experiment resulting in following IR spectra. Can you analyze it and fill the following table? Are their any impurities found?
Peak Position cm-1 |
Bond Type |
|

Transcribed Image Text:Wavenumbers (cm-1)
4000
3500
3000
2500
2000
1500
1000
500
-2
0
$34.97
N
4
6
1248.08
8
10
12-
14-
16
18
20
22-
24
26
1678.11
1503.63
1487.15
1440.18
%Transmittance
1038.47
2977.99
2905.83
1604.99
1359.44
1140.00
1112.25
933.58
877.83
794.48
1460.69
1765.04
3077.21
3344.59
966.30
3224.27
2784.35
2717.68
2673.35
2616.36
2480.21
1859.63
1818.47
1308.71
1071.24
744.04 718.36

Transcribed Image Text:Reaction 1
da
CH₁
ZnO (nanoparticles)
Heat
ol
CH₂
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