Lab 2- TLC
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Experiment #2
Thin Layer Chromatography
Lab Partner – Teaching Assistant – Date Performed – October 5, 2023
Date Due - October 12, 2023
Experimental Objective
Thin layer chromatography (TLC) is performed in the first stage of the experiment to determine which solvent is best for separating aspirin, acetaminophen, and caffeine. Subsequently, the components of a combination are identified using TLC and the specified solvent.
Procedure
Setting up the TLC plates and determining the better solvent
One centimeter down from the TLC plate's bottom, a horizontal line was drawn. From this line, vertical lines were drawn to show the locations of the samples (aspirin, acetaminophen, and caffeine). After that, the samples were moved via the capillary tubes onto the TLC plate. The sample size was intended to be as small as a tiny dot because any larger or smaller would have distorted the findings. For comparison, two solvents were used: 1:1 Hexanes:Ethyl Acetate and 95% ethyl acetate with 5% acetic acid. The TLC jars received around 3 mL of solvent poured to them. Subsequently, the plates were inserted into their corresponding jars, with the upper part of each plate resting on the jar. The solvent was about 1 cm from the top when the plate was taken out. Where the solvent ceased was marked on the plate.
The spots on the TLC plate were visible using the short wave UV section. To find the Rf values, the spots were lightly drawn with a pencil. We compared the two plates to see which solvent would produce the best outcomes. Since the samples separated, 95% ethyl acetate and 5% acetic acid seemed to be the best solvent. Working unknown sample #247
In a test tube, about 28 mg of unknown #247 were dissolved in 1 milliliter of 95% ethanol. The unknown solution was made and spotted on a second TLC plate. A ruler was used to measure from the beginning line to the center of each sample dot after all of the plates had been produced.
The sample's Rf values were ascertained using the dots. To ascertain which compounds made up unknown #247, the values of the unknown and the known substances were compared.
Results
Figure 1:
Drawn depictions of all 3 TLC plates involved
The below equation was used to calculate the Rf values for all spots on all plates, given the dimensions and measurements of the observed plates which are pictured above. The measurements and calculated data are shown in the below tables.
Table 1:
Data from TLC plates in 1:1 Hexanes:Ethyl acetate
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Related Questions
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THE PICTURE UPLOADED SERVES AS A GUIDE, DO THE SAME THING BASED FROM THE PIC.
Procedure:
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Centrifuge the mixtures for 3 mins. and decant the supernatant liquid. Add 10 drops of DI water and 10 drops of 6M HNO3. Stir and boil the mixture in a hot water bath for 5 mins.
centrifuge the mixture for 3 mins.
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Objective:
Apparatus and Materials:
Procedure :
Calculate the exact mass of NaOH needed to prepare 1.0L of 0.25N NaOH for standardization. Show your computations.
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Place the weighed amount of NaOH into the 500 mL volumetric flask and add distilled water until it reaches the mark.
Agitate and transfer the solution into the reagent bottle.
Add again distilled water to the same volumetric flask until it reaches the mark and pour it to the same reagent bottle, thus having a total volume of 1.0 L.
Label the reagent bottle, 0.25N NaOH.
Data and Computations:
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