Lab CHM 260
Lab CHM 260
3) Based on the molecular structure and by using the table provided in the introduction
( or any other IR Correlation charts available)
i)Predict the location of three peaks you might expect from its IR spectrum.
Compound Peaks
Aromatic ring 1600,1500 (w) - stretch
Alkenes 1680-1640 (m,w) - stretch
Carboxylic acid 1760-1670 (s) stretch
4) Indicate what bonds were responsible for all the peaks you identified in (i)
Compound Bonds
Aromatic ring C=C
Alkenes C=C
Carboxylic acid C=O
Questions
1) Explain why a background spectrum must be run before obtaining sample spectrum
It is to make sure we only get the data from our sample only and not a spectrum
containing other chemical or substances.
2) Why must “neat” liquids and not aqueous solutions be used on salt plates?
It is because the presence of water in aqueous solution might cause the salt plate to
dissolve and produce the emission of a broad OH peak, which will mask numerous
other peaks.
DATASHEET EXPERIMENT 3
Name: Muhammad Afif Aiman Bin Azahar Date: 11/11/2022
Stud ID: 2020477846 Group:
Name and model of instrument : FOURIER TRANSFORM INFRARED
SPECTROSOCOPY (FTIR)
Cyclohexane C6H12
C-H 1470 – 1350 (V) 1449.55cm-1
Acetone C3H6O
C=O 1760 – 1670 (s) 1709.38cm-1
3) i) Unknown number:
ii) Molecular formula of unknown compound :