Computerized Data Acquisition of a Second Order Reaction Essay

The rambles at which replys occur depend on the opus and the temperature of the reaction mixture. Usually the localize of reaction is found to be comparative to the concentrations of the reactants raised to a exponent.1 There are many reactions that have a invest law in the form of (1) v = kAaBbAccording to reference1 the power to which the concentration of a species (product or reactant) is raised in a pace law of this nature is the order of the reaction with respect to that species. In equality (1) original order with respect to A and first order with respect to B however, the boilersuit reaction is the sum of the individual orders. Thus we have a turn order reaction. In this experiment a hexacyanoferrate(III) ion (Fe(CN)63-) oxidizes ascorbic dosage (C6H8O6) by the following(a) reaction (2) 2Fe(CN)63- + C6H8O6 = 2Fe(CN)64- + C6H6O6 + 2H+The reaction above is of a first order reaction at room temperature with respect to individual reactants therefore the reaction stoich iometry and rate law at time t are (3) aA + bBproducts and (4) -dA = kA Bwhere A represents the concentration of ascorbic acid and B represents the concentrations of Fe(CN)63- at time t. For this experiment we will use an integrated rate law in the form of (5) ln A = b A0 a B0 kt + ln A0where A0 and B0 are the initial concentrations of C6H8O6 and Fe(CN)63- and a=1 and b=2. From equation (5), it is possible to calculate the second-order rate changeless k by plotting ln A/B against time (find slope of line where b=2 and a=1). EDTA in this experiment is used as a masking agent to hide metal ions that would normally interfere with the abridgment in this reaction. Thus the absorbance of Fe(CN)63- at time t is given by (6) Absorbance = 1012 Fe(CN)63-The oxidation of C6H8O6 by Fe(CN)63- involves a mechanism that consists of 3 criterions.2 In the first step, the ascorbate ion (AH-) is cursorily formed by ionization of the ascorbic acid. (7) AH2 AH + H+Following the ionization is the s low rate-determining step, the oxidation of the ascorbate ion to an ascorbate free radical (AH) (8) Fe(CN)63- + AH-Fe(CN)64- + AH During the final step, an electron is rapidly transferred from the ascorbate free radical to the hexacyanoferrate(III) anion, producing dehydroascorbic acid (A) (9) Fe(CN)63- + AH- Fe(CN)64- + A + H+The slow rate-determining step is an ionic reaction between Fe(CN)63- and AH-. According to reference3, the specific rate constant of an ionic reaction in aqueous issue depends on dickens factors the ionic strength I of the final result and on the charges ZA and ZB of the ionic species reacting to for the initiate complex. (10) log k = log k0 + 1.02ZAZB I1/2ExperimentalAll reagents in this experiment were of reagent grade. Mass measurements were taken on a Shimadzu Libror AEG-120 analytical scale with an uncertainty of 0.0001. Manual data acquisition was taken with a Barnstead/ turner SP-830 spectrophotometer and a stopwatch. The computerized data acquisi tion was completed by a Cary 50 Bio. The experiment began by preparing four solutions of 1 x 10-3 M of K3Fe(CN)6 with alter concentrations of NaNO3 0.025 M, 0.05 M, 0.1 M and 0.2 M.This was completed by dissolving 0.0329245 (0.001) g of K3Fe(CN)6 with the specified concentrations of NaNO3 and deionized weewee in a 100 mL volumetric flask. A 25 mL aliquot of each solution was transferred into a 250 mL Erlenmeyer flask and the temperature of the aliquot was recorded. Next, a 500 mL 2.5 x 10-4 M solution of ascorbic acid was prepared by utilise a standardized 0.01 M HNO3 solution dissolved in 0.005 g of EDTA and deionized water. A 25 mL aliquot was transferred into each of the four 100 mL beakers by using a 25 mL pipet.The spectrophotometer was set to 418 nm and the absorbance reading was zeroed by using deionized water as a standard. The ascorbic acid in the beaker was poured into the K3Fe(CN)6 solution and the timer was immediately started. The Erlenmeyer flask was swirled for 2- 3 seconds before pouring the reacting mixture into a 1-cm cuvette. The cuvette was conditioned with the reacting solution 4 times before being primed(p) into the sample holder of the spectrophotometer. An absorbance reading was taken at 30 seconds and all(prenominal) 30 seconds thereafter for a total of 6 minutes. The same cover was implemented with the Cary 50 Bio except that each sample was analyzed by the computer for 7 minutes and 53 seconds. Data/Results