The phosphate in a 3.000-g sample of industrial detergent was precipitated by the addition of 1.000 g of AgNO3. The solution was filtered and filtrate, upon addition of 1.00 mL of 0.01 M fecl3, required 18.23 mL of 0.1377 M KSCN for titration to the end point. (a) what type of precipitation titrimetry was used. (b) which served as the indicator (c) the color at the endpoint
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The phosphate in a 3.000-g sample of industrial detergent was precipitated by the addition of 1.000 g of AgNO3. The solution was filtered and filtrate, upon addition of 1.00 mL of 0.01 M fecl3, required 18.23 mL of 0.1377 M KSCN for titration to the end point. (a) what type of precipitation titrimetry was used. (b) which served as the indicator (c) the color at the endpoint (d) the weight percent of phosphate in the detergent.
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- A mixture of NaBr, Nal and NaNO3 weighs 0.6500 g. With AgNO3, a precipitate of the two halides is obtained and is found to weigh 0.9390 g. When heated in a current of C2, the precipitate is converted entirely to AgCi weighing 0.6566 g. What is the %NaNO3 in the original sample?1.0 g of a solid sample known to contain a mixture of NaOH and Na2CO3 is dissolved with distilled water and completed to 25 mL. By adding 2 drops of phenolphthalein (pT = 9.0) to the solution obtained, it was titrated with 0.107 M calibrated HCl solution, and the consumption was determined as 10.6 mL. Subsequently, 2 drops of methyl red (pT = 4.4) were added onto the same solution and titrated, the consumption was determined as 6.1 mL. Accordingly, calculate the amount of NaOH and Na2CO3 in the sample solution as% (a/a) by writing the related reactions. (Na: 23, C: 12, O: 16, H: 1 g / mol)A saturated solution of magnesium hydroxide is prepared and the excess solid magneisum hydorixed is allowed to settle. A 25.0 mL aliquot of the saturated solution is withdrawn and transfered to a flask, two drops of inficator are added. A 0.00053 M HCL is dispensed from a buret into a solution. The solution changes color after the addition of 13.2 mL. What is the solubility product, Ksp, for magensium hydroxide?
- If a sample of silver coin weighing 0.2500 g gives a precipitate of AgCl weighing 0.2991 g, What wt of AgI could have been obtained from the same wt of sample?The level of dissolved oxygen in a water sample can be determined by the Winkler method. In a typical analysis, a 100.0-mL sample is made basic, and treated with a solution of MnSO4, resulting in the formation of MnO2. An excess of KI is added, and the solution is acidified, resulting in the formation of Mn2+ and I2. The liberated I2 is titrated with a solution of 0.00870 M Na2S2O3, requiring 8.90 mL to reach the starch indicator end point. Calculate the concentration of dissolved oxygen as parts per million of O2.1.00 grams of table salt was dissolved in 100 mL water and excess AgNO3 reagent was added and yielded 2.3789 grams of precipitate. Calculate the percentage of NaCl in the table salt.
- A sample of soluble salt weighs 1.2 g and contains chloride, bromide and iodide. With AgNO3, a precipitate is obtained which weighs 0.4500 g. On heating this precipitate with Cl2 gas, the AgBr and AgI are converted to AgCl, and the precipitate then weighs 0.3300 g. A similar sample, when treated with palladous chloride, precipitates only PdI2, and this precipitate weighs 0.0900 grams. (*)Find the approximate percentage of chlorine, bromine and iodine in the sampleIron (55.845 g/mol) can be determined gravimetrically by precipitation as Fe(OH)3 (106.867 g/mol) and subsequent inflammation of the precipitate to convert it to Fe2O3 (159.69 g/mol). A 0.7873 g sample to be analyzed was weighed and transferred to a 400 mL beaker, where it was dissolved in 50 mL of H2O and 10 mL of 6M HCl. Then 2 mL of concentrated HNO3 was added to the solution. After boiling to remove excess HNO3 and nitrogen oxides, the solution was diluted to 200 mL, brought to boiling, and Fe(OH)3 was precipitated by the slow addition of 1:1 NH4OH solution until an odor of NH3 was detected (indicating the presence of excess NH3 in the medium). The solution was left in a water bath at 80 ºC for 30 min at rest. The precipitate was then filtered and washed with several portions of hot 1% m/v NH4NO3 until no Cl– was detected in the wash water. Finally, the precipitate was ignited at 500-550 °C, then left in a desiccator to cool and weighed as Fe2O3, resulting in a mass of 0.4512 g.…A 0.6407g sample containing chloride and iodide ions gave a silver halide precipitate weighing 0.4430g. This precipitate was then strongly heated in a stream of chlorine gas to convert the AgI to AgCl; on completion of this treatment, the precipitate weighed 0.3181g. Calculate the percentage of chloride and iodide in the sample.
- The purity of a pharmaceutical preparation of sulfanildamide (C6H4N2O2S), is prolonged oxidizing the sulfur in the sample to SO2 and bubbling this SO2 through a solution of H2O2 which converts it to H2SO4. The acid is titrated with a standard solution of NaOH (0.1251 M) until the end point with bromothymol blue, which changes color when both protons of the acid sulfuric have been neutralized. Calculate the purity of the preparation in % by weight given that a sample of 0.5136 g required 50.00 mL of the NaOH solutionAs part of a soil analysis on a plot of land, a scientist wants to determine the ammonium content using gravimetric analysis with sodium tetraphenylborate, Na+B(C6H5)4−. Unfortunately, the amount of potassium, which also precipitates with sodium tetraphenylborate, is non‑negligible and must be accounted for in the analysis. Assume that all potassium in the soil is present as K2CO3 and all ammonium is present as NH4Cl. A 5.095 g soil sample was dissolved to give 0.500 L of solution. A 150.0 mL aliquot was acidified and excess sodium tetraphenylborate was added to precipitate both K+ and NH4+ ions completely. B(C6H5)4-+K+⟶KB(C6H5)4(s) B(C6H5)4-+NH4+⟶NH4B(C6H5)4(s) The resulting precipitate amounted to 0.269 g. A new 300.0 mL aliquot of the original solution was made alkaline and heated to remove all of the NH4+ as NH3. The resulting solution was then acidified, and excess sodium tetraphenylborate was added to give 0.129 g of precipitate. Find the mass percentages of NH4Cl and…The amount of sulfate in a solid sample was determined by first dissolving 562.2 mg of sample in water, and then precipitating the sulfate by the addition of 25.00 mL of 0.022 96 M BaCl2. The precipitate was filtered from the solution and the remaining Ba2+ was titrated with 16.52 mL of 0.014 57 M EDTA. What was the mass percent of sulfate in the solid?