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Second Order Reaction Kinetics

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Second Order Reaction Kinetics
Abstract

The objective of this experiment was to determine if the specific rate constant of the reduction reaction of hexacyanoferrate (III) ion with ascorbic acid (C6H8O6) is affected by the ionic strength of the solution and the charges of the ion species within the solution. A Cary Bio 50 Spectrophotometer and its associated software was used to measure the absorbance of the solution at a wavelength of 418 nm. Analysis of the data collected supports the conclusion that the ionic strength of the solution and the charges of ions on the activated complex have a direct relation to the rate constant. The experimental value of 2.237 for the ionic strength of 0.025 M when compared to the literature value of 1.72 in a similar experiment by Nobrega and Rocha, has a percent error of 30%. For the ionic strength of 0.05 M, the percent error between the experimental value 2.851 and the literature value of 2.58 was 11%. The ionic strength of 0.1 had an error of -1% between the literature value of 3.97 and the experimental value 3.924. For the ionic strength of 0.2 there was a -23% error between the experimental value of 5.301 and the literature value of 6.89 (Nobrega, 1997). The experimental value of the product of the charges of the ions in the activated complex, 2.1, was lower than the expected value 3, which could be due to the shielding of the charges on the reactants due to the ions witihin the solution.

Introduction

The reduction of the hexacyanoferrate (III) ion with ascorbic acid to form the dehydroascorbic acid (C6H6O6) has the following reaction:

2[Fe(CN)6]3- + C6H8O6 = 2[Fe(CN)6]4- + C6H6O6 + 2H+ [1]

Which follows the mechanism: (fast) [2]

AH2 k1 k-1 AH-+H+ FeCN63-+ AH- k2 FeCN64-+ AH∙ (slow) [3]
(fast) [4]

FeCN63-+ AH∙ k3 FeCN64-+ A+H+

Where AH2 is the ascorbic acid, AH- is the ascorbate

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