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. Then, centrifuge it for 1 minute. On the side, weight a boiling test tube containing 2 boiling chips. When the separation is complete, remove the small test tubes from the centrifuge and decant the supernatant into the boiling test tube. Add 1 mL of deionized water to the small test tube containing the precipitate and mix it and centrifuge it for 60 seconds.
Using a measuring cylinder, add 50cm3 of 1.0mol dm-3 sulphuric(VI) acid to the thyme extract in the conical flask. 8. Titrate the solution in the conical flask with the potassium manganate(VII) solution until a pale pink colour persists for 10 seconds. 9. Repeat the titration until there are two titres within 0.1cm3 of each other.
Add 10 ml of ph 10 buffer to the same Erienmeyer flask. Start swirling immediately to dissolve, 7. Add 15 ml of water next. Use a squeeze bottle so you can wash the inside walls of the flask. 8.
Cylinder was rinsed with distilled water. * * 2. 2.0 ppm standard: 2.00 mL of 10.0 ppm phosphate solution was placed in a 25 mL graduated cylinder and diluted to exactly the 10 mL mark with distilled water then poured into a plastic cup labeled 2. Cylinder was rinsed with distilled water. * 3.
Set min temperature to 15-18C c. Time should range from 0-250 seconds 7. Press DISPLAY to accept all values 8. Heat up 200mL of water in a microwave for about two minutes 9. Place hot water on a hot plate to keep warm 10. Nest one Styrofoam cup in another 11.
The other lab partner should add the 20 mL water to the 100 mL beaker and stir for one minute. 19. Measure another 20 mL water using the graduated cylinder. 20. Add another 20 mL water to the 100 mL beaker and stir for one minute.
Using another 125-mL flask, 60-mL of 0.3622 M potassium hydroxide in ethanol was deposited. Both flasks were clamped in a temperature-controlled bath regulated at 50.0˚C. The solutions were then set in the temperature bath for ten minutes to equilibrate. An empty 250-mL Erlenmeyer flask was also clamped in the same water bath. In another flask 50-mL of ice water was deposited with three-drop phenolphthalein.
In the first part, five 100 mL flasks of 5 mL ligand solution, 5 mL 2 M sodium acetate, 4 mL 3 M NH2OH, and 1-5 mL Fe2+ solution are diluted with water. The absorption spectrum for varying concentrations of Fe2+ are measured using a spectrophotometer and the data is graphed in Excel. The slope of the line is ε in the Beer-Lambart equation A = εcl. In the second part of the experiment, eleven flasks containing diluted stock solutions of Fe2+ and ligand are mixed with 5 mL 2 M sodium acetate and 4 mL 3 M NH2OH and diluted with water. The absorption spectrum is measured using a spectrophotometer and the data is graphed in Excel.
Materials and Methods Part 1 For the cation elimination test first 10 drops of potassium, iron (III), zinc (II), copper (II), and cobalt (II) were added to 5 centrifuge tubes and the color was recorded. Then for the metal hydroxide test, 6 M NaOH was added drop wise till a precipitate was formed. Each solution except potassium formed a precipitate, so then 10 additional drops of NaOH were added to the remaining solutions. Tubes were cleaned with distilled water and 6 M HCL. Next was the ammonia test 10 drops of each metal solution were added to new centrifuge tubes and 15 M NH4OH was added until the solution changed color or a precipitate was formed.
After 1 hour we boiled a beaker of water on the hot plate (for Benedict’s and AgNO3 test). 5. We took all of the dialysis sacs