Pb(NO3)2 = 1.25 g Pb(NO3)2 X 1 mol Pb(NO3)2 X 1 mol PbI 2 X 461.0 g PbI2 331.2 g Pb(NO3) 2 1 mol Pb(NO3)2 1 mol PbI2 =1.739 g od PbI2 3.The theoretical yield of the precipitate in the reaction is 1.735 g of potassium iodide. Observation Table Material | Mass with no substance | Mass with substance | Physical property of Reactants | Beaker A | 66.97g | 68.22g including KI | White Powder | Beaker B | 65.91 g | 67.16 g including Pb(NO3)2 | Solid white crystals
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oxide 5) sodium iodide 6) strontium fluoride 7) lithium sulfide 8) radium chloride 9) calcium oxide 10) aluminum phosphide 11) potassium sulfide 12) lithium bromide 13) strontium phosphide 14) barium chloride 15) sodium bromide 16) magnesium fluoride 17) sodium oxide 18) strontium sulfide 19) boron nitride 20) aluminum nitride 21) cesium oxide 22) rubidium iodide 23) magnesium oxide 24) calcium bromide 25) lithium iodide 26) berylium bromide 27) potassium oxide 28) strontium iodide 29) boron fluoride
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Chemicals 0.20 M potassium iodide (KI solution)‚ 0.0050 M sodium thiosulfate (Na2S2O3 containing 0.4% starch indicator)‚ 0.10 M potassium peroxydisulfate (K2S2O8) . Procedure Part 1 : Finding the Rate Law and Rate Constant 1. The most accurate piece of glassware that allows
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CSEC CHEMISTRY NOTES ON SOLUBILITY OF COMPOUNDS IN WATER and SATURATED SOLUTION Reference: Chemistry‚ a Concise Revision Course for CXC by Anne Tindale From Chemistry for CSEC by Tania Chung-Harris and Mike Taylor Factors that influence solubility Temperature * The solubility of solids in liquids generally increases as temperature increases. * The solubility of gases in liquids generally decreases as temperature increases. (gases are less soluble in warm water than in cold water)
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iodometry‚ where iodine “is produced in-situ from the quantitative oxidation of iodide and then subsequently titrated with thiosulfate solution‚”2 being the difference from the former type of iodine titration. Iodometry is more widely used‚ as in this experiment‚ because there are only a few strong reducing agents; thus few iodometric determinations. (2) As mentioned earlier‚ iodometry involves the oxidation of iodide ion; it is added in excess to the oxidizing agent being determined. This would
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monochloride solution from a burette and mix. Then add about 5 mL of a 2.5% solution of mercuric acetate in glacial acetic acid‚ which will act to catalyse the reaction. Insert the stopper which has been previously moistened with a solution of potassium iodide. Keep in a dark place for 3 minutes to allow the unsaturated fatty acid residues of the
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iodine produced from potassium iodide by manganese(III) hydroxide. 2Mn(OH)3(s) + 2I-(aq) + 6 H+(aq) －－＞ 2Mn2+(aq) + I2(aq) + 6H2O(l) Sodium thiosulphate is used as the titrant. Success of the method is critically dependent upon the manner in which the sample is manipulated. At all stages‚ every method must be made to assure that oxygen is neither introduced to nor lost from the sample. Furthermore‚ the sample must be free of any solutes that will oxidize iodide or reduce iodine. Chemicals:
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C25-C29 C30-C39 C40-C49 C50-C100 A Chemical formula Synonyms CAS number AgCl3Cu2 dicopper silver trichloride 69569-0 AgClO4 silver perchlorate 7783-93-9 AgF silver fluoride 7775-41-9 AgF2 silver difluoride 7775-41-9 AgI silver iodide 7783-96-2 AgIO3 silver iodate 7783-97-3 AgMnO4 silver permanganate 7783-98-4 AgN3 silver azide 13863-88-2 AgNO3 silver nitrate 7761-88-8 Ag2O silver oxide 1301-96-8 AgONC silver fulminate 5610-59-3 AgSNC silver thiocyanate 14104-20-2
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10.0 EXPERIMENT ON DETERMINATION OF DISSOLVED OXYGEN Sl. No. Contents Preamble 10.1 Aim 10.2 Introduction 10.2.1 Environmental Significance 10.3 Principle 10.4 Materials Required 10.4.1 Apparatus Required 10.4.2 Chemicals Required 10.5 Sample Handling and Preservation 10.5.1 10.6 Precautions Procedure 10.6.1 Preparation of Reagents 10.6.2 Testing of Water Sample 10.7 Calculation 10.7.1 Table 10.7.2 Data Sheet 10.8 Interpretation of Results 10.9 Inference 10.10 Evaluation
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Abstract Tetramethylammonium iodide was dissolved in a mixture of of Iodine and 95% ethanol while gently heated in a fume hood. Once cooled‚ crystals started to form in the beaker‚ which were then collected and washed with hexane through a series of processes involving vacuum filtration. Then a mixture of 5mh of the crystals and 5ml of 95% ethanol was created and tested on a slice of potato to analyse the iodine content. After‚ with sodium thiosulphate in the buret‚ the iodide solution was titrated until
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