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.
6. How many moles of NaCl are in 250. mL of a 0.200 M solution? 1. 15.8 g of KCl is dissolved in 225 mL of water. Calculate the molarity.
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.
c. Prepare the solution by dissolving 38.90 grams of ZnI2 with 500 mL of water. d. 0.0125/0.25 = 0.05 L = 50 mL. This produces 0.0125 moles of ZnI2 5. Exercise 5: a. (0.125)(0.1) = 0.0125 moles of solute b. Pour 50 mL of the stock solution to get the number of moles needed.
Obtain another 50-mL beaker and add 0.05g of Chromium(III) Nitrate to the beaker. Then, add 17 mL of distilled water and mix until the solid is dissolved. 3. Obtain a final 50-mL beaker and add 0.05 grams of the unknown substance to the beaker. Add 17 mL of distilled water and mix with a stir bar until the solid is completely dissolved.
The two unknown solids are weighed to a mass of 0.15g each. The unknown solids are dropped carefully into the corresponding Erlenmeyer flask wit 50mL of distilled water. The solid in the water must be dissolved and afterwards add 10 drops of Bromecresol green to indicate the change of color when the solution has been titrated. The flask should start with a blue tint. HCl is carefully dropped into the Erlenmeyer flasks with the primed pipette until the solution turn to a green tint.
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.
Obtain beaker filled with 250 mL of HCl and 5 pennies. 2. Get a pipette and remove 10 mL of that solution (HCl + Zn) and place it in a 100 mL beaker. 3. Add color indicator 4.
Single Replacement Reaction Laboratory Modified from Glencoe Chemistry - Matter and Change, Glencoe McGraw-Hill, 2002 Objectives Observe a single replacement reaction Measure the masses of iron and copper Determine the mole ratios and the limiting reactant Chemicals Iron filings (Fe) – 20 mesh Copper(II) sulfate pentahydrate, (CuSO4·5H2O) Distilled water Materials Stir rod 100-mL beaker 250-mL beaker 25-mL graduated cylinder Weigh paper Balance Hot plate Beaker tongs Wire mesh insulated pad screen Distilled water wash bottles |Lab Data - Reaction of Copper(II) Sulfate and Iron | | Mass of empty 100-mL beaker |(g) | | | Mass of 100-mL beaker
Enough water should be added so that the flask is full to the 250 ml mark Tightly wrap the top of the flask with a Parafilm when finished 2. Set up the titration apparatus 3. Fill a dry 50 ml buret with EDTA solution using a small