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Chromatography practical discussion
Chromatography practical discussion
Chromatography practical discussion
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1. Dissolve 1 g of a mixture in 2 ml of dichloromethane.
2. Add 1 ml of 5% HCL in a test tube and shake it for 2 minutes.
3. Le the 2 layers separate. Remove the top layer (aqueous solution) and transfer it to a clean test tube. Label it as TT-1.
4. To the bottom layer add 1 ml of portion of 5% HCL and shake it. When 2 layers are separated, transfer it (top layer) to TT-1 and cork it. This should contain your organic base. Save it for next lab period.
5. The remaining dichloromethane solution should contain the organic acid and neutral compound.
6. To this tube add 1 m of water, shake it and transfer top layer to TT-1 and save it.
7. To the remaining dichloromethane solution add 1 ml of 5 % NaOH, shake it and transfer top layer to a new test tube and label TT-2.
8. To the
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To the remaining dichloromethane solutions add 1 ml of water, shake it and transfer top layer to TT-2 cork it and save it.
10. To the dichloromethane if needed add enough fresh dichloromethane to make it 1 ml.
11. Then add 1 g of anhydrous sodium sulfate (solid) and shake it. Decant liquid into another test tube, label it as TT-3 corks it and save it.
Recovery of compounds; (acid, base and neutral)
1. Cool solution in TT-1 and add 10% NaOH dropwise while still on ice bath until the solution is base to litmus paper (turns blue).
2. Collect solid by suction filtration, wash solid with cold deionized water.
3. Scrape solid onto a watch glass and dry it (solid should be a base).
4. Cool the NaOH extract in TT-2 on ice bath and add 10% HCl until the solution is acidic to litmus paper (red).
5. Collect solid by suction filtration, wash with cold water. Scrape solid out on a watch glass and dry it (solid should be your solid).
6. From TT-3, evaporate dichloromethane in a hot water bath in the hood. When it is dry it should contain the natural compound.
7. Determine melting points of all three compounds and match these up with melting points of known compounds from the list and identify
Each subsequent trial will use one gram more. 2.Put baking soda into reaction vessel. 3.Measure 40 mL vinegar. 4.Completely fill 1000 mL graduated cylinder with water.
Then titrate with the sodium thiosulfate solution as in the standardization procedure, adding 6 drops of starch indicator near the end of the titration. Record the volume of thiosulfate solution used in the titration. Make a duplicate
neutralize 35ml of our base. Once we weighed out the KHP we then dissolved it
Using your finger, gently tap the tubes to mix the Luria broth with the cell suspension. The test tubes will need to rest for approximately five to fifteen minutes in a room temperature environment.
Then add 6 drops of Winkler's solution #2 into the test tube with cold water.
catalase solution to the mixture. Now, pour the contents of test tube into a Nalgene bottle capable
First, label the three test tubes number one, two, and three. For each test tube, you need to add three mL of vegetable oil. Now for test tubes numbers one and two, you need to add five mL of water. Only for test tube number three add two mL of lipase enzyme. For only test tubes number two and three, add a pinch of bile salts. Once this is all done, mix the tubes by flicking the bottoms. Afterwards, place all three tubes in a water bath for only thirty minutes. Once this is all completed, you can then record and analyze the
Put the amount of 0.1M cobalt (II) chloride hexahydrate that fills the end of a spatula into a test tube. Then add 2mL of 95% ethanol. Tap the end of the test tube to mix the solution and record the pertinent data in section 1 of the Data Table. Discard the solution in the appropriate container as directed to you by your lab instructor.
1.In the lab experiment, the instructions told us to adulterate the concentration of hydrogen peroxide and Chlorine with some water.
3.) Divide your 30g of white substance into the 4 test tubes evenly. You should put 7.5g into each test tube along with the water.
In a 100ml beaker place 50mls of water, measure the temperature of the water and record this initial temperature onto a table. Set the timer and add one teaspoon of Ammonium Nitrate to the water, stir this continuously until the Ammonium Nitrate has dissolved.
Mixed melting point was used to confirm the identity of the product. The smaller the range, the more pure the substance. When the two substances are mixed; the melting point should be the same melting range as the as the melting range obtained after filtering. If the mixed melting point is lower one taken from the crystals, then the two substances are different.
2. In the large beaker, put water and boil it completely. After that, remove the beaker from heat. 3. Sample tubes (A-D) should be labeled and capped tightly.
Add 5 g crushed nutmeg and 50 mL hexane-isopropanol into a flask and warm for 15 minutes.
tube. Add 6 mL of 0.1M HCl to the first test tube, then 0.1M KMnO4 and