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Paul [167]
4 years ago
8

A certain reaction has the following general form. aA → bB At a particular temperature and [A]0 = 2.80 ✕ 10−3 M, concentration v

ersus time data were collected for this reaction, and a plot of 1/[A] versus time resulted in a straight line with a slope value of +3.40 ✕ 10−2 L mol−1 s−1. (a) Determine the rate law, the integrated rate law, and the value of the rate constant for this reaction. (Rate expressions take the general form: rate = k . [A]a . [B]b.) rate law:
Chemistry
1 answer:
Delvig [45]4 years ago
8 0

Answer:

Rate law: r=k[A]^2

Integrated rate law: \frac{1}{[A]}=kt+ \frac{1}{[A]_0}

Rate constant: k=3.40x10^{-2}\frac{L}{mol*s}

Explanation:

Hello,

In this case, since the slope is obtained by plotting 1/[A] and it has the units L/(mol*s) or 1/(M*s), we can infer the reaction is second-order, therefore, its rate law is:

r=k[A]^2

The integrated rate law:

\frac{1}{[A]}=kt+ \frac{1}{[A]_0}

That is obtained from the integration of:

\frac{d[A]}{dt}=-k[A]^2

And of course, since the slope equals the rate constant, its value is:

k=3.40x10^{-2}\frac{L}{mol*s}

Regards.

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Answer:

Equilibrium constant expression for \rm 2\; H^{+}\, (aq) + {CO_3}^{2-}\, (aq) \rightleftharpoons H_2CO_3\, (aq):

\displaystyle K = \frac{\left(a_{\mathrm{H_2CO_3\, (aq)}}\right)}{\left(a_{\mathrm{H^{+}}}\right)^2\, \left(a_{\mathrm{{CO_3}^{2-}\, (aq)}}\right)} \approx \frac{[\mathrm{H_2CO_3}]}{\left[\mathrm{H^{+}\, (aq)}\right]^{2} \, \left[\mathrm{CO_3}^{2-}\right]}.

Where

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Explanation:

<h3>Equilibrium Constant Expression</h3>

The equilibrium constant expression of a (reversible) reaction takes the form a fraction.

Multiply the activity of each product of this reaction to get the numerator.\rm H_2CO_3\; (aq) is the only product of this reaction. Besides, its coefficient in the balanced reaction is one. Therefore, the numerator would simply be \left(a_{\mathrm{H_2CO_3\, (aq)}}\right).

Similarly, multiply the activity of each reactant of this reaction to obtain the denominator. Note the coefficient "2" on the product side of this reaction. \rm 2\; H^{+}\, (aq) + {CO_3}^{2-}\, (aq) is equivalent to \rm H^{+}\, (aq) + H^{+}\, (aq) + {CO_3}^{2-}\, (aq). The species \rm H^{+}\, (aq) appeared twice among the reactants. Therefore, its activity should also appear twice in the denominator:

\left(a_{\mathrm{H^{+}}}\right)\cdot \left(a_{\mathrm{H^{+}}}\right)\cdot \, \left(a_{\mathrm{{CO_3}^{2-}\, (aq)}})\right = \left(a_{\mathrm{H^{+}}}\right)^2\, \left(a_{\mathrm{{CO_3}^{2-}\, (aq)}})\right.

That's where the exponent "2" in this equilibrium constant expression came from.

Combine these two parts to obtain the equilibrium constant expression:

\displaystyle K = \frac{\left(a_{\mathrm{H_2CO_3\, (aq)}}\right)}{\left(a_{\mathrm{H^{+}}}\right)^2\, \left(a_{\mathrm{{CO_3}^{2-}\, (aq)}}\right)} \quad\begin{matrix}\leftarrow \text{from products} \\[0.5em] \leftarrow \text{from reactants}\end{matrix}.

<h3 /><h3>Equilibrium Constant of Concentration</h3>

In dilute solutions, the equilibrium constant expression can be approximated with the concentrations of the aqueous "(\rm aq)" species. Note that all the three species here are indeed aqueous. Hence, this equilibrium constant expression can be approximated as:

\displaystyle K = \frac{\left(a_{\mathrm{H_2CO_3\, (aq)}}\right)}{\left(a_{\mathrm{H^{+}}}\right)^2\, \left(a_{\mathrm{{CO_3}^{2-}\, (aq)}}\right)} \approx \frac{\left[\mathrm{H_2CO_3\, (aq)}\right]}{\left[\mathrm{H^{+}\, (aq)}\right]^2\cdot \left[\mathrm{{CO_3}^{2-}\, (aq)}\right]}.

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