Title | The Rate Law in Chemical Kinetics |
---|---|
Course | Chemistry of Solutions |
Institution | Dawson College |
Pages | 7 |
File Size | 150.5 KB |
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The Rate Law in Chemical KineticsI. IntroductionThe rate of a reaction is the change in concentration of a reactant or a product per unit of time. The goal of this experiment was to determine the rate law, which only takes into account the reactants, and the constant k of the following reaction:2 I(...
The Rate Law in Chemical Kinetics Experiments #8
Lab section: 20 202-NYB-05
Date the experiment was performed: Thursday, April 12 th 2018 Date of lab report submission: Thursday, April 19 th, 2018
I. Introduction The rate of a reaction is the change in concentration of a reactant or a product per unit of time. The goal of this experiment was to determine the rate law, which only takes into account the reactants, and the constant k of the following reaction: (aq) (aq) 2−¿ 2 SO ¿ 2−¿ O ¿ I 2(aq)+¿ −¿+S 2 ¿ ¿ 2 I (aq) 2−¿ n −¿ ] Rate = k [ I ¿ ]m[ S 2 O¿8 It is not possible to determine the rate law of this reaction without doing an experiment. In 2−¿ this lab, the method of initial rates was used. By maintaining the concentration of S 2 O 8¿ −¿ constant for the first five runs, the order of the reaction (m) with respect to I ¿ was found. −¿ ¿ remained constant and the concentration For the last four runs, the concentration of I 2−¿ ¿ of changed. S 2 O8 If starch is added only to the previous reaction, the color change would happen too fast. Therefore, a second reaction, which occurred at the same time as the other one, was used: (aq) (aq) 2−¿ S 4 O¿ −¿+¿ 2−¿ ¿ O ¿ I 2(aq) → 2 I (aq) 2 S2 ¿ In this reaction,
2−¿ S 2 O¿3
used up the I 2
; thus, delaying the apparition of the deep blue
2−¿ was consumed, the mixture turned blue. Since its initial S 2 O¿3 concentration could be calculated from the values already known, it was possible to determine color. When all of the
the initial rate of the reaction with the following formula: 2−¿ S2 O¿3 ¿ ∆¿ −1 R0 = ∙¿ 2
¿ ∆ t=time taken for the mixture ¿ change ¿
II. Procedure Refer to the Laboratory Manual.
III. Data and Results Table 1: Reagent Concentrations Reagent
Concentration (mol/L)
KI
0.180
Na 2 S2 O 3
0.0036
(NH 4 )2 S 2 O 8
0.180
Table 2: Time taken for each run Run
Time (s)
1
26.54
2
30.28
3
36.66
4
44.45
5
60.93
6
28.62
7
33.44
8
40.05
9
67.89
Table 3: Initial Concentrations −¿ ¿ I ¿ (mol/L) ¿ ¿
Run
1
0.0720
−¿ ¿ I Ln ¿ ¿ ¿
2−¿ S 2 O¿8 (mol/L) ¿ ¿ ¿
2−¿ S 2 O¿8 Ln ¿ ¿ ¿
-2.631
0.0720
-2.631
2
0.0600
-2.813
0.0720
-2.631
3
0.0480
-3.037
0.0720
-2.631
4
0.0360
-3.324
0.0720
-2.631
5
0.0240
-3.730
0.0720
-2.631
6
0.0720
-2.631
0.0600
-2.813
7
0.0720
-2.631
0.0480
-3.037
8
0.0720
-2.631
0.0360
-3.324
9
0.0720
-2.631
0.0240
-3.730
Table 4: The Initial Rates and the k Run
R0
Ln R0
k ( L/mol ∙ s )
1
0.000014
-11.21
0.0026
2
0.000012
-11.34
0.0028
3
0.0000098
-11.53
0.0028
4
0.0000081
-11.72
0.0031
5
0.0000059
-12.04
0.0034
6
0.000013
-11.28
0.0029
7
0.000011
-11.44
0.0031
8
0.0000090
-11.62
0.0035
9
0.0000053
-12.15
Table 5: Temperature and Average K Temperature (K)
295.5
Average K (mol/L ∙ s)
0.0030
IV. Sample Calculations Run 1 1) Number of moles of M=
2−¿ S 2 O 3¿
n V
n 0.0150 n=0.000054 mol
0.0036=
2) Concentration of M=
n V
2−¿ ¿ S 2 O3
0.0031
0.000054 0.0750 M =0.00072 mol / L M=
3) Concentration of
2−¿ reacted S 2 O¿8
2−¿ S2 O8¿ ¿ S ¿ 2−¿ ¿ 2O¿3 ¿ ¿ ¿ 2−¿ S 2 O¿8 ¿ ¿ 2−¿ ¿ S 2 O8 ¿ ¿ 4) Initial reaction rate 2−¿ ¿ S2 O 3 ¿ ∆¿ 1 R0 = ∙ ¿ 2 1 0.00072 R0 = ∙ 2 26.54 R0=0.000014 mol/ L ∙ s
5) Initial concentration of
−¿¿ I
M 1 ∙ V 1=M 2 ∙ V 2 0.180 ∙30.0 =M 2 ∙ 75.0 M 2=0.0720 mol / L 6) Initial concentration of
2−¿ ¿ S 2 O8
M 1 ∙ V 1=M 2 ∙ V 2 0.180 ∙30.0 =M 2 ∙ 75.0 M 2=0.0720 mol / L 7) k value 2−¿ 1 −¿ ¿ ] Rate = k [ I ¿ ]1[ S 2 O8 0.000014 =k ∙ 0.0720 ∙ 0.0720 k =0.0026 L/mol ∙ s
8) Average k average k=
0.0026 + 0.0028+ 0.0028 + 0.0031 + 0.0034 + 0.0029 + 0.0031 + 0.0035 + 0.0031 9
average k=0.0030 L/mol ∙ s
V. Conclusion The objective of this experiment was to determine the rate law and the constant of the following reaction: ( aq) ( aq) 2 SO2−¿ ¿ O 2−¿ I ¿ 2(aq)+ ¿ −¿+ S 2 ¿ ¿ 2 I (aq)
2−¿ −¿ It was achieved since the rate law and its constant were: Rate = k [ I ¿ ]1[ S O ¿ ]1. The 2 8 orders were found by taking the slope of the graphs. For this lab, there were some sources of error. For example, when the solution of flask 2 was poured into flask 1, it is likely that not all of the 30 mL got in the first flask, since spilling occurred. Therefore, next time, a beaker should be used instead of flask 1. Since the beaker has a larger opening, it is less probable for spilling to occur. In addition, there was always a delay between the moment the solution turned dark blue and the reaction time to record the time. This delay added more seconds to the times recorded....