t=0 min, [A]=.80 M; 8 min, [A]=.60 M; 24 min, [A]=.35 M; 40 min, [A]=.20 M.
a) Establish the order of the reaction.
b) What is the value of the rate constant, k?
c) Calculate the rate of formation of B at 22 min.
Any help would be greatly appreciated, thank you.
For the reaction A---%26gt;2B+C, the following data are obtained for [A] as a function of time:?
(a)
Assume a simple power law kinetic:
r(A) = d[A]/dt = - k·[A]ⁿ
The corresponding integrated forms of the rate late law are:
ln( [A]₀/[A]) = k·t for n =1
[A]₀⁽¹ ⁻ⁿ⁾- [A]⁽¹ ⁻ⁿ⁾= (1-n)·k·t for n≠1
Standard procedure would be to plot [A]⁽¹ ⁻ⁿ⁾ (or ln[A] ) versus t for various n. The graph which yields a straight line is the one with correct reaction order n.
But plotting is a bit difficult here. So assume n and calculate calculate rate constant for each time. If k is (almost) constant assumed n was correct. If k tend to increase or decrease with time assumed n was incorrect
Assume n=1
k = ln( [A]₀/[A]) / t
t = 8min
k = ln( 0.8M / 0.6M) / 8min = 0.3596min⁻¹
t = 24min
k = ln( 0.8M / 0.35M) / 24min = 0.3444min⁻¹
t = 40min
k = ln( 0.8M / 0.2M) / 40min = 0.3466min⁻¹
That looks good. So reaction is first order:
r(A) = d[A]/dt = - k·[A]
(b)
You could simply take the average of the values calculated in (a). To minimize deviation from data points by linear regression.
Fitting
ln( [A]₀/[A]) = k·t
to the data points leads to
k = ( Σ ln([A]₀/[A])·t ) / ( Σ t² )
= (ln(0.8/0.6)·8min + (0.8/0.35)·24min + ln(0.8/0.2)·40min ) / ((8min)² + (24min)² + (40min)² )
= 0.03464min⁻¹
(c)
ln( [A]₀/[A]) = k·t
%26lt;=%26gt;
[A] = [A]₀· exp(-k·t)
Hence rate of reaction of A is
r(A) = -k·[A] = - k · [A]₀· exp(-k·t)
According to reaction equation 2moles of B are formed per mole A consumed.
Hence
d[B] = -2·d[A]
%26lt;=%26gt;
r(B) = d[B]/dt = -2·d[A]/dt = -2·r(A)
=%26gt;
r(B) = 2 · k · [A]₀· exp(-k·t)
at t=22min
r(B) = 2 · 0.03464min⁻¹ · 0.8M · exp(-0.03464min⁻¹
·22min)
= 0.02586 M/min = 0.02586 mol/Lmin
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