5.0g of an alloy of copper was dissolved in one litre of dilute sulphuric acid. In 20 ml of this solutoin, excess of potassium iodide was added and final solution required 25ml hypo solutoion for titration. In 20ml of potassium dichromate solution (containing 2.4 g of pottassium dichromate per litre of solution), sulphuric acid and excess KI were added. This solution required 30 ml of same hypo solution. Calculate the percentage by weight of copper present in the allov
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- While working in a metal processing facility, Letlen had accidentally mixed two metal vatstogether creating an alloy. One vat was labeled for cadmium, while the other was not. It canbe assumed that these are of pure metal composition. To identify this metal, Letlen took 1.000 g of the homogenous alloy sample composed ofcadmium and the unknown metal, dissolved, and diluted it to exactly 100.0 mL in avolumetric flask. A 20.00-mL aliquot was taken and titrated this using 22.82 mL of 0.05000M EDTA. In a second 20.00-mL aliquot, the Cd was masked through the addition of HCN/NaCN buffer.The titration of the unknown metal in the aliquot required 15.13 mL of EDTA.MW: Cd (112.411 g/mol) a. Calculate the moles of Cd and the moles of unknown metal in the 20.00-mL aliquot.b. Calculate the moles of Cd and the moles of unknown metal in the sample.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) the weight percent of phosphate in the detergentUsing basic conditions, MnO4- can be used as titrant for the analysis of Mn2+, with both the analyte and the titrant ending up as MnO2. In the analysis of a mineral sample for manganese, a 0.5165-g sample is dissolved, and the manganese is reduced to Mn2+. The solution is made basic and titrated with 0.03358 M KMnO4, requiring 34.88 mL to reach the endpoint. Calculate the %w/w Mn in the mineral sample. Answer: % Mn =
- It is required to know the concentration of an aqueous solution of H2SO4 that appeared in the laboratoryChemistry III and it's unlabeled. To this end, a student of analytical chemistry carried out the followingProcedure: He took 5.00 mL of a fresh and standardized solution of 0.525M NaOH and brought them to a250.0 mL balloon to be completed with distilled water. Subsequently, he poured 15.00 mL of the solutionH2SO4 of unknown concentration in an Erlenmeyer flask and added 2 drops of phenolphthalein.Using a burette filled with the last NaOH solution, he noticed that when adding 39.40 mL of the hydroxidethe Erlenmeyer solution reached a faint but permanent pink. With the above dataDetermine the concentration and pH of the H2SO4 solution.Q: The concentration of the sulphate ion in a mineral water can be determinedby the turbidity which results from the addition of excess BaCl2, to a quantityof measured sample. A turbidometer used for this analysis has been standardisedwith a series of standard solutions of NaSO4. The following resultswere obtained:Standard solution Conc. (SO4)2− (mg/L) Reading of turbidometerS0 0.00 0.06S1 5.00 1.48S2 10.00 2.28S3 15.00 3.98S4 20.00 4.61i. In supposing that a linear relationship exists between the readings takenfrom the apparatus and the sulphur ion concentration, derive an equationrelating readings of the turbidometer and sulphate concentration(method of least squares).ii. Calculate the concentration of sulphate in a sample of mineral waterfor which the turbidometer gives a reading of 3.67.A 3.25 g sample of an iron-containing mineral was dissolved in an acid medium and calibrated to 500 mL. A 25.00 mL aliquot was titrated with 0.0025 M KMnO4 spending a volume of 9.32 mL. Subsequently, a 25.00 mL aliquot was passed through a Walden reducer to later titrate it with the same permanganate solution, using a volume of 14.15 mL for the titration. Determine the percentage of Fe(III) in the sample and report it as % Fe2O3
- 1ml of 1mg/ml of diluted aspirin powder solution is titrated by 0.005M NaOH. Before titration, 5 ml ethanol, 14 ml CO2 free water, and 4 drops bromothymol blue indicator is added into diluted aspirin powder solution. Mass of 0.005M NaOH used is obtained by weight titration = 1.1384g . [Molar mass of aspirin =180.15]; for solution, 1g=1mL at 25 degree Celcius. Calculate the purity of the powder.A shipment of containing NaOH (40 g/mol) and Na2CO3 (106 g/mol) was declared to contain less than 10 % impurity. However, Noel is suspicious that the declared impurity is higher. Being the best and brightest employee of the year, Noel weighed 1.000 g sample, dissolved in 50.0 mL of distilled water and titrated with cold 0.5000 M HCl. With Phenolphthalein as indicator, the solution turns colorless after the addition of 30.00 mL of the acid. Methyl Orange is then added, and 5.00 mL more of the acid is required before this this indicator changes color. Calculate the following: a. Determine the volume of the acid to fully neutralize NaOH (final answer up to one decimal place) =calculate the mass of Sn when 50 mL of a sample containing Sn2+ is titrated with 42.00 mL of 0.0150M MnO4- to reach endpoint
- 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 Ksp of magnesium hydroxide?The arsenic in a 1.010 g sample of a pesticide was converted to H3AsO4 by suitable treatment. The acid was then neutralized, and exactly 40.00 mL of 0.06222M AgNO3 was added to precipitate the arsenic quantitatively as Ag3AsO4. The excess Ag in the filtrate and in the washings from theprecipitate was titrated with 10.76 mL of 0.1000MKSCN; the reaction wasAg+ + SCN-→ AgSCN(s) Calculate the percent AsO3 in the sample.The sulfur content of insoluble sulfides that do not readilydissolve in acid can be measured by oxidation with Br2to SO42.25Metal ions are then replaced with Hby an ion-exchange column,and sulfate is precipitated as BaSO4with a known excess ofBaCl2. The excess Ba2is then titrated with EDTA to determinehow much was present. (To make the indicator end point clearer,a small, known quantity of Zn2also is added. The EDTA titratesboth the Ba2and the Zn2.) Knowing the excess Ba2, we cancalculate how much sulfur was in the original material. To analyzethe mineral sphalerite (ZnS, FM 97.46), 5.89 mg of powderedsolid were suspended in a mixture of CCl4and H2O containing1.5 mmol Br2. After 1 h at 20 C and 2 h at 50 C, the powder dis-solved and the solvent and excess Br2were removed by heating.The residue was dissolved in 3 mL of water and passed throughan ion-exchange column to replace Zn2with H. Then 5.000 mLof 0.014 63 M BaCl2were added to precipitate all sulfate as BaSO4.After the addition of…