Then, I filled the tube to the shoulder with distilled water. I added one nitrate tablet. I capped the tube and I mixed until the tablet disintegrates. I wait 5 minutes for the color to develop. Then I compared the blue color of the solution to the nitrogen color chart: L = 40 lbA/6" soil, M = 160 lb A/6" soil, and H = 320 lb A/6"
Record the mass of thyme used. 2. Using a measuring cylinder, add 50cm3 of 1.0mol dm-3 sulphuric(VI) acid and boil gently for 5 minutes. 3. Allow the mixture to cool for a few minutes then filter it, using either gravity or vacuum filtration.
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.
Results and Discussion For the first part of the experiment (Part A), five different 100 mL volumetric flasks were each filled with 1,2,3,4 and 5 mL of iron (II) solution. Then 5 mL of YY ligand, were poured to each of the five flasks. Each flask had 5 mL of 2M sodium acetate and 4 mL of 3M NH2OH. Then the whole solution was diluted up to the 100 mL fill mark with distilled water. This was the solution that was used in order to obtain the absorption spectrum for each of the different iron (II) ligand examples different flasks.
Ryan Hopkins TA: Carla Terry Chem 1212K lab INTRODUCTION The purpose of this research is to identify an inorganic acid that was selected by chance. It was bottled in a small glass jar labeled as number three. In the quest to find what was in the jar several experiments were performed. The scientific approaches performed were purifying the sample, analyzing the percent halide, percent NH3, prep and standardization of 0.1M Na2S2O3, and the examination of percent Cobalt (III) using 0.1 M Thiosulfate and the analysis of an unknown Fe (III) salt. SYNTHESIS 3 Purifying an unknown solid by recrystallization involved preparing cobalt amine chloride product.
Materials & Methods Identifying the unknown compound solution (#2314) first required the identification of each individual solution. One drop of each solution was added to five individual wells of a spot plate. Next, three drops of 3M hydrochloric acid (to be referred to from now on as HCl). The spot plate was then cleaned, and the procedure above was recreated two more times, the second test done by adding 3M ammonium hydroxide (NH4OH), and the third by adding 1 drop of dimethylglyoxime (DMG). All color observations were recorded and compared to the known behaviors of the focus metals.
Materials and Methods To begin, .4001 grams of Na2HPO4 and .4081 grams of NaH2PO4 solid was added together into a clean, dry 150 mL glass beaker. Then, approximately 50 mL of distilled water was added to the mixture, and the phosphate solids were stirred until fully dissolved. The last ingredient added to the beaker was exactly 20 drops of the liquid .04% bromothymol blue solution. Using the Vernier pH probe, the initial pH of this soluton was found to be 7.10. After obtaining three clean, dry 50mL glass beakers (Labeled one of each “yellow,” “blue,” and “green.”) approximately 5.00 mL of the solution from the 150mL beaker was added to all three with a volumetric pipet.
In this lab, two different titrations were performed with three different antacids to determine which brand is the most effective at the cheapest price. The antacids were ground up separately and approximately 0.2 grams of it was placed in a flask. Methyl Orange, an indicator, and a stir bar were added into the flask. The flask was then put on a stir plate which was under a buret with 0.1M hydrochloric acid. The acid was poured into the flask until there was a permanent pink colour.
Each of the 3 unknowns was distributed by dispensing 2ml of sample solution in to three test tubes. Once in the test tube 400ug of each reagent was dispensed in the separate solutions. The test tube with Benedict ’s reagent was heated to 65 degrees C and let cool to see color change. The results from this test were then compared to our known nutrients and recorded in Table 2. Determining Absorbency of Starch To determine the absorbency of starch; a
Once the procedure was performed three times, the collected iron fillings mass was obtained by using the digital weighing scale. After removing the iron fillings, the sand was removed next by using the property of sand that the sand was completely insoluble in the water. The iron free solids mixture was dissolved in 15.00 mille liters of distal water and heated by using stove top in a beaker. The solution was mixed for a while the benzoic acid and salt were allowed to dissolve completely and solubility was enhanced by heating the solution. The solution was decanted into another beaker.