Calculations
Calculations
Calculations
Initial standard:
−1
M (bet )=551.48 gmol
m(bet )=0.5130.0005 g % ∆ m=0.0975
m
n(bet )= % ∆ n=% ∆ m
M
0.513
n(bet )=
551.48
n(bet )=0.000930 9 ×10−7 mol % ∆ n=0.0975
n
c=
v
% ∆ c=% ∆ n+% ∆ v
diluted standards:
vi
c f =c i % ∆ c f =% ∆ ci + % ∆ v i+ % ∆ v f
vf
0.002
c f (1)=0.00186 % ∆ c f =0.138+2.5+0.04
0.1
c f (1)=0.0000372± 1× 10−6 mol l−1 % ∆ c f =2.68
0.004
c f (2)=0.00186 % ∆ c f =0.138+1.25+0.04
0.1
c f (2)=0.0000744 ±1 ×10−6 mol l −1 % ∆ c f =1.428
0.006
c f (3)=0.00186 % ∆ c f =0.138+0.833+0.04
0.1
c f (3)=0.000112± 1× 10−6 mol l−1 % ∆ c f =1.01
0.008
c f (4 )=0.00186 % ∆ c f =0.138+0.625+0.04
0.1
c f (4 )=0.000149 ±1 ×10−6 mol l−1 % ∆ c f =0.803
0.01
c f (5)=0.00186 % ∆ c f =0.138+0.5+ 0.04
0.1
−6 −1
c f (5)=0.000186 ±1 ×10 mol l % ∆ c f =0.678
calculation of absorbance, concentration relationship.
Io
log 10 =l c
I
Io
log 10 = Absorbance=|¿|
I
|¿|1257 c−0.01071
secondary standard:
m
n= % ∆ n=% ∆ m
M
0.983
n=
551.48
−6
n=0.00178 ±1 ×10 mol % ∆ n=0.0699
n
c= % ∆ c=% ∆ n+% ∆ v
v
vi
c f =c i % ∆ c f =% ∆ ci + % ∆ v i+ % ∆ v f
vf
0.03
c=0.00357 % ∆ c f =0.1099+0.1+0.04
0.5
−7
c=0.000214 ± 4 ×10 mol l
−1
% ∆ c f =0.2199
Temperature vs concentration relationship:
Linear fit:
|¿|1257 c−0.01071
−5
∆ ICPT =( 0.000247−0.000230 )=1.70 ×10
Arrhenius equation.
−E a
k = A e RT
By combining the Arrhenius equation for the rate constant, k with the
1st order kinetics equation we get a very accurate relationship
( )
−Ea
− A e RT t
[ c ] =[c ]o e
substituting values, we get…
−226.3
T
−3.74 e
c=0.0002168 e
[c ]o=0.0002168
− At=−3.74
t=3 ×60=180 s
A=0.0208
−Ea
=−2263
R
−1
R=8.314 JK mol
−1
Ea =18814 J mol