Hydrogen sulfide \(\left(\mathrm{H}_{2} \mathrm{S}\right)\) is a common and troublesome pollutant in industrial wastewaters. One way to remove \(\mathrm{H}_{2} \mathrm{S}\) is to treat the water with chlorine, in which case the following reaction occurs: $$ \mathrm{H}_{2} \mathrm{S}(a q)+\mathrm{Cl}_{2}(a q) \longrightarrow \mathrm{S}(s)+2 \mathrm{H}^{+}(a q)+2 \mathrm{Cl}^{-}(a q)$$ The rate of this reaction is first order in each reactant. The rate constant for the disappearance of \(\mathrm{H}_{2} \mathrm{S}\) at \(28^{\circ} \mathrm{C}\) is \(3.5 \times 10^{-2} \mathrm{M}^{-1} \mathrm{s}^{-1}\) . If at a given time the concentration of \(\mathrm{H}_{2} \mathrm{S}\) is \(2.0 \times 10^{-4} \mathrm{M}\) and that of \(\mathrm{Cl}_{2}\) is \(0.025 \mathrm{M},\) what is the rate of formation of \(\mathrm{Cl}^{-} ?\)

Short Answer

Expert verified
The rate of formation of Cl⁻ is \(3.5 \times 10^{-6} \mathrm{M}\cdot\mathrm{s}^{-1}\).

Step by step solution

01

Write down the rate law for the reaction

Since the reaction is first order with respect to both reactants, the rate law can be written as: \(Rate = k[\mathrm{H}_{2}\mathrm{S}][\mathrm{Cl}_{2}]\) where \(Rate\) is the reaction rate, \(k\) is the rate constant, and \([\mathrm{H}_{2}\mathrm{S}]\) and \([\mathrm{Cl}_{2}]\) are the concentrations of H₂S and Cl₂, respectively.
02

Calculate the reaction rate using given values

We are given that the rate constant \(k = 3.5 \times 10^{-2} \mathrm{M}^{-1} \mathrm{s}^{-1}\), the concentration of H₂S at that time \([\mathrm{H}_{2}\mathrm{S}] = 2.0 \times 10^{-4} \mathrm{M}\), and the concentration of Cl₂ at that time \([\mathrm{Cl}_{2}] = 0.025 \mathrm{M}\). Plug these values into the rate law: \(Rate = (3.5\times 10^{-2} \mathrm{M}^{-1} \mathrm{s}^{-1})(2.0 \times 10^{-4} \mathrm{M})(0.025 \mathrm{M})\) Now calculate the rate: \(Rate = 1.75 \times 10^{-6} \mathrm{M}\cdot\mathrm{s}^{-1}\)
03

Determine the stoichiometric relationship between the reactants and products

From the balanced reaction, we can see that for every 1 mole of H₂S that reacts, 2 moles of Cl⁻ are produced: \(\mathrm{H}_{2}\mathrm{S}(aq) + \mathrm{Cl}_{2}(aq) \longrightarrow \mathrm{S}(s) + 2\mathrm{H}^{+}(aq) + 2\mathrm{Cl}^{-}(aq)\) So, the rate of production of Cl⁻ is twice the rate of disappearance of H₂S.
04

Calculate the rate of formation of Cl⁻

Using the stoichiometric relationship and the calculated rate of reaction, we can find the rate of formation of Cl⁻: \(Rate_{formation}\, of\, \mathrm{Cl}^{-} = 2 \times Rate_{disappearance}\, of\, \mathrm{H}_{2}\mathrm{S}\) \(Rate_{formation}\, of\, \mathrm{Cl}^{-} = 2 \times 1.75 \times 10^{-6} \mathrm{M}\cdot\mathrm{s}^{-1}\) Now calculate the rate: \(Rate_{formation}\, of\, \mathrm{Cl}^{-} = 3.5 \times 10^{-6} \mathrm{M}\cdot\mathrm{s}^{-1}\) So, the rate of formation of Cl⁻ is \(3.5 \times 10^{-6} \mathrm{M}\cdot\mathrm{s}^{-1}\).

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Most popular questions from this chapter

\(\begin{array}{l}{\text { (a) What is meant by the term elementary reaction? }} \\ {\text { (b) What is the difference between a unimolecular }} \\\ {\text { and a bimolecular elementary reaction? (c) What is a }}\end{array}\) \(\begin{array}{l}{\text {reaction mechanism?}(\mathbf{d}) \text { What is meant by the term rate- }} \\ {\text { determining step? }}\end{array}\)

Many primary amines, RNH \(_{2},\) where \(R\) is a carbon-containing fragment such as \(C H_{3}, C H_{3} C H_{2},\) and so on, undergo reactions where the transition state is tetrahedral. (a) Draw a hybrid orbital picture to visualize the bonding at the nitrogen in a primary amine (just use a \(C\) atom for \(^{4} \mathrm{R}^{\prime \prime}\) . (b) What kind of reactant with a primary amine can produce a tetrahedral intermediate?

Urea \(\left(\mathrm{NH}_{2} \mathrm{CONH}_{2}\right)\) is the end product in protein metabolism in animals. The decomposition of urea in 0.1 \(\mathrm{M} \mathrm{HCl}\) occurs according to the reaction $$\mathrm{NH}_{2} \mathrm{CONH}_{2}(a q)+\mathrm{H}^{+}(a q)+2 \mathrm{H}_{2} \mathrm{O}(l) \longrightarrow 2 \mathrm{NH}_{4}^{+}(a q)+\mathrm{HCO}_{3}^{-}(a q)$$ The reaction is first order in urea and first order overall. When \(\left[\mathrm{NH}_{2} \mathrm{CONH}_{2}\right]=0.200 M,\) the rate at \(61.05^{\circ} \mathrm{C}\) is \(8.56 \times 10^{-5} \mathrm{M} / \mathrm{s}\) , (a) What is the rate constant, \(k ?\) units of \(s^{-1}\) . (c) Calculate the half-life of the reaction. (d) How long does it take for the absorbance to fall to 0.100\(?\)

(a) What are the units usually used to express the rates of reactions occurring in solution? (b) As the temperature increases, does the reaction rate increase or decrease? (c) As a reaction proceeds, does the instantaneous reaction rate increase or decrease?

Dinitrogen pentoxide \(\left(\mathrm{N}_{2} \mathrm{O}_{5}\right)\) decomposes in chloroform as a solvent to yield \(\mathrm{NO}_{2}\) and \(\mathrm{O}_{2} .\) The decomposition is first order with a rate constant at \(45^{\circ} \mathrm{C}\) of \(1.0 \times 10^{-5} \mathrm{s}^{-1} .\) Calculate the partial pressure of \(\mathrm{O}_{2}\) produced from 1.00 \(\mathrm{L}\) of 0.600 \(\mathrm{MN}_{2} \mathrm{O}_{5}\) solution at \(45^{\circ} \mathrm{C}\) over a period of 20.0 \(\mathrm{h}\) if the gas is collected in a \(10.0-\mathrm{L}\) container. (Assume that the products do not dissolve in chloroform.)

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