After that, dissolve the sample in 2 mL of deionized water and shake the test tube for 1 to 1 ½ minutes to dissolve the solid. Place another dry test tube in a 50mL beaker and weigh it. Find a bottle of barium iodide and record the name and molar mass. Then, weight out either anhydrous barium iodide or barium iodide dehydrate into this test tube and dissolve is it in 2 mL of deionized water. Pour the contents of one of the test tubes into the other and a reaction should occur and you should see a white precipitate of barium sulfate form.
Allow the mixture to cool for a few minutes then filter it, using either gravity or vacuum filtration. (We shall be using vacuum filtration.) Wash the residue in the funnel once with a little water and collect all the filtrate. 4. Pour all the filtrate and washings into a 250cm3 volumetric flask.
Then 5mL of HCl was added to copper to completely remove all traces of zinc. Once the bubbling had stopped, the rest of the liquid was decanted away from the copper. Then the copper recovery set up was put together using tubing, Buchner funnel, filter paper and suction flask. Then the filter paper was weighed before placing it in the funnel and wetted down. The aspirator was turned to medium high, and then the copper was poured onto wetted filter paper.
Materials: 3 beakers Thermometer 3 Alka-Seltzer tablets Stopwatch Mortar and pestle Source of hot water Ice cubes Graph paper Procedures: Hot water- Run water from the hot tap until it is hot as possible Fill beaker with 80 mL of hot water Use thermometer to take temperature of water. Record in data table. Remove 1 Alka-Seltzer tablet from package Drop into the water. Measure the time it takes for the tablet to completely dissolve. BE READY WITH THE STOPWATCH.
In another flask 50-mL of ice water was deposited with three-drop phenolphthalein. Using a volumetric pipet 50-mL of the 1-bromopropane was added into the empty flask in the bath. By the same method 50-mL of potassium hydroxide was delivered to the same flask while swirling the contents and remaining in the water bath. A 10-mL aliquot was immediately removed from the mixture and added to the ice water containing the phenolphthalein. When the pipet was half emptied into the ice water a timer was started.
Part A: Spectroscopy 1. 0.05g of Iron(III) Nitrate in a 50-ml beaker. Add 17 mL of distilled water to the beaker and mix with a stir rod until the solid is completely dissolved. 2. Obtain another 50-mL beaker and add 0.05g of Chromium(III) Nitrate to the beaker.
Procedure Step 1, Obtain acid, in a 100 ml Erlenmeyer flask add 35 ml of .2M HCl solution. Step 2, add an indicator to the acid, select the flask and add 2 drops of phenolphthalein indicator. Step 3, Fill buret with NaOH, obtain a 50 ml buret and fill with .2M NaOH solution.Step 4, Titrate NaOH into HCl until end point, record initial buret volume and add NaOH (quickly at first then slowly) until the HCl solution turns pink and record the final buret volume of NaOH in buret. Step 5, repeat steps 1-4 using pH meters, add a pH meter to the acid solution. Record several points of pH and NaOH added (especially near equivalence point) to be use later to prepare a titration curve.
At first we dried the crucible in the flame three times and let it come to a constant mass by measuring the weight each time. To determine percentage of water in Epsom salt, we measured about 2g of the salt into three different, dried crucibles. The crucibles were first heated gently, then intensely to drive off all the water. The final data was reported as percent hydrate with 95% confidence level. RESULTS & DISCUSSION Weights of the crucible.
At the same time, place the second thermometer bulb just at about the bottom of the beaker 6. Record the initial temperature near the bottom 7. Place ONE drop of food coloring at the bottom of the beaker after the initial 90 second beaker warm-up period *LEAVE THE BEAKER BURNER ON THE HOT PLATE THROUGHOUT THE 3 MINUTES OF TEMPERATURE MEASUREMENTS 8. Record your observations 9.
Compare the MPs of the once recrystallized and the twice recrystallized trimyristin. After the hydrolysis has proceeded for 45 minutes, allow the flask to cool to RT and pour the contents into a 50 mL beaker containing 8 mL of water. Carefully, in the hood, add dropwise with stirring, 2 mL of concentrated HCl (caution: corrosive liquid/noxious vapors). Myristic acid should precipitate. Cool the beaker in ice water for 10 min, with stirring, and collect the solid by vacuum filtration on a small Hirsch funnel.