The Spectrophotometric Determination of an Equilibrium Constant

With these absorbance numbers a concentration curve was constructed and the unknown solution was determined by finding the point of absorbance on the curve.

After this, the solution was poured into a volumetric flask just about to the 1dm3 line and then it was left there to cool to the same temperature as the room before filling precisely to the 1dm3 line with distilled water. The molar mass of CuSO4.5H20 was 249.5 so that means 249.5g of copper sulphate was needed to dissolve, in order to make a standard solution, into 1dm3of distilled water. Following this, a linear dilution of the CuSO4.5H2O was made in order to be used to make a calibration curve after using the colorimeter to write down the absorbance of each sample. A linear dilution is diluted with distilled water in order for it to make the concentration weaker and weaker. For this investigation, the dilutions made ranged from 0.01 to 0.1 M/l . It was essential to only make up 10cm3

In reference to the analysis of anions, Table 1 shows that a precipitate was formed when our unknown was combined with HNO3 and AgNO3, thus indicating the presence of a chloride ion. Because our unknown did not form a precipitate due to HCl and BaCl2, separate, effervesce, or smell, we concluded that neither sulfate, nitrate, carbonate nor

Spectrophotometer; the finding of protein concentration of an unknown sample of BSA, and by using the standard curve.

Hypothesis: The stoichiometric ratio of the reactants in the chemical synthesis of the (2, 4-pentanedianato) iron (III) complex ion is 3:1.

The Beers Law calibration experiment used many concentrations of crystal violet solutions. Each of these solutions were test and analyzed in order to determine the absorbance of each concentration The results were than graphed and produced a slope of 1.00E05 with an intercept of -2.21E-02.

AP Chemistry Background The solubility product constant, Ksp, is a particular type of equilibrium constant. The equilibrium is formed when an ionic solid dissolves in water to form a saturated solution. The equilibrium exists between the aqueous ions and the undissolved solid. A saturated solution contains the maximum concentration of ions of the substance that can dissolve at the solutions temperature. A knowledge of the Ksp of a salt is useful, since it allows us to determine the concentration of ions of the compound in a saturated solution. This allows us to control a solution so that precipitation of a compound will not occur, or to find the concentration needed to cause a precipitate to form. The solubility product which will be

Solutions of 6M H2SO4, 6M NH3, 6M HCl, 6M NaOH, and 1.0 M of NaCl, 1M Fe(NO3)3, 1M NiSO4, 1M AgNO3, 1M KSCN, 1M Ba(NO3)2, and 1M Cu(NO3)2 were given in separate test tubes. The color of possible precipitates, ions, acid-base behaviour, odor and solubility rules were conducted and were reported in Table 1. The key information about a mixture of two solutions was

Table 2: Addition of KSCN, Fe(NO₃)₃and Na₂HPO₄to Iron (III) Thiocyanate and Change of Direction of Equilibrium

This calibration curve then created an equation that allowed for the unknown concentration of the FeSCN2+ ions to be determined.

Seven test tubes were labeled numerically with 2 mL of VO3- and H2SO42- added to each tube. A small pea size portion of solid Na2SO3 was added to the first test tube. Then, 20 drops of distilled water were added to the second test tube. In the third test tube, 20 drops of (.2 M) NaBr were added. Then, to drops of (.2 M) NaNO2 were added into the fourth test tube. A small portion of Fe(NH4)2(SO4)2 * 6H2O was added into the fifth test tube. The sixth test tube had 20 drops of (.2 M) H2Cr2O4 added, where the seventh test tube was the control tube with no additional chemicals added. All the test tubes were left to react for 3 minutes and then heated in a heated bath for approximately 20 minutes.

In this experiment, two reactions were run to determine the molar absorptivity and the equilibrium constant of FeSCN2+. The main principles used in this lab are equilibrium, LeChatlier’s Principle, Beer’s Law and Spectrocopy. The first reaction was run to completion using LeChatier’s Principle and the second reaction was run to equilibrium. A spectrophotometer was used to measure absorbances. Using a graph of absorbance versus concentration of FeSCN2+ was used to determine that the molar absorptivity constant was 3670. Beer’s Law was used to determine that the average equilibrium constant was 33.1793.

The lab performed required the use of quantitative and analytical analysis along with limiting reagent analysis. The reaction of Copper (II) Sulfate, CuSO4, mass of 7.0015g with 2.0095g Fe or iron powder produced a solid precipitate of copper while the solution remained the blue color. Through this the appropriate reaction had to be determined out of the two possibilities. Through the use of a vacuum filtration system the mass of Cu was found to be 2.1726g which meant that through limiting reagent analysis Fe was determined to be the limiting reagent and the chemical reaction was determined to be as following:-

Instead, the relationship between the increase in Fe3+ and the increase in FeSCN2+ was used to determine Kc with the help of spectroscopy and mathematical manipulation of the equilibrium expression. The experiment started with a pure solution of KSCN. Knowing that KSCN decomposes into the reactant of interest, SCN-, the 50 mL of KSCN was rewritten as 50 mL of 1.2E-4 M SCN- since this value is written in terms useful to the experiment. After this, successive additions of 1 mL of 0.1 M Fe3+ was added to the SCN- solution, mixed, and measured for absorbency at 445 nm. FeSCN2+ has a characteristic orange color, allowing for the spectroscopy of the resulting solution to be recorded since this color falls within the visible range capabilities of the spectrometer.

Procedure: Part 1 1. Initial colours of Fe(NO3)3 and KSCN were recorded in an observation table. 2. A stock solution of FeSCN2+ was made by measuring 40mL of distilled water in a 50mL beaker. Using a titrant, 1mL of Fe(NO3)3 and 2mL of KSCN were added to the beaker.