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The reaction $$ 0^{\circ} \mathrm{C}, $$ These relationships hold only if there is a very small amount of \(\mathrm{I}_{3}^{-}\) present. What is the rate law and the value of the rate constant? (Assume that rate \(=-\frac{\Delta\left[\mathrm{H}_{2} \mathrm{SeO}_{3}\right]}{\Delta t} )\)

Short Answer

Expert verified
The rate law for the reaction between hydrogen selenite and iodate is given by \(Rate = 2 \times 10^{-1}[\mathrm{IO_3^-}]\), and the value of the rate constant is \(2 \times 10^{-1} \frac{L}{mol\cdot min}\).

Step by step solution

01

Determine the balanced chemical equation

The balanced chemical equation for the reaction between hydrogen selenite and iodate can be written as follows: \[ 2\mathrm{IO_3}^- + 5\mathrm{H_2SeO_3} + 12\mathrm{H^+} \rightarrow I_3^- + 5\mathrm{Se} + 6\mathrm{H_2O} \] Step 2: Determine the order of the reaction with respect to each reactant
02

Determine the order of the reaction with respect to each reactant

To determine the order of the reaction with respect to \(\mathrm{IO_3^-}\), we will analyze the experimental data provided. We can see that when the concentration of \(\mathrm{IO_3^-}\) is doubled, the reaction rate doubles as well. This indicates that the reaction is first-order with respect to \(\mathrm{IO_3^-}\). The rate expression for \(\mathrm{IO_3^-}\) is given by: \[ Rate = k[\mathrm{IO_3^-}]^n \] Now, let's analyze the experimental data provided for \(\mathrm{H_2SeO_3}\). We can see that when the concentration of \(\mathrm{H_2SeO_3}\) is doubled, the reaction rate remains the same. This indicates that the reaction is zero-order with respect to \(\mathrm{H_2SeO_3}\). Thus, the rate law can be expressed as: \[ Rate = k[\mathrm{IO_3^-}]^n[\mathrm{H_2SeO_3}]^0 \] Step 3: Calculate the rate constant
03

Calculate the rate constant

Given that rate \(= -\frac{\Delta[\mathrm{H_2SeO_3}]}{\Delta t}\). We can use the experimental data and the rate expression we found in step 2 to calculate the rate constant. Let's use the data from the first row of the table: \(Rate = 4.0 \times 10^{-4} \frac{mol}{L \cdot min}\) \[\left[\mathrm{IO_3^-}\right] = 2.0 \times 10^{-3} \frac{mol}{L}\] Using the rate expression: \[Rate = k[\mathrm{IO_3^-}]^n\] We can plug in the values and find the rate constant: \[4.0\times10^{-4} = k(2.0\times10^{-3})^n\] Solving for k, we get: \[k = \frac{4.0\times 10^{-4}}{(2.0\times 10^{-3})}\] Thus, the rate constant, k, equals \(2 \times 10^{-1} \frac{L}{mol\cdot min}\). Step 4: Write the final rate law expression
04

Write the final rate law expression

Combining our findings from Steps 2 and 3, we can now write the complete rate law for the reaction: \[Rate = (2 \times 10^{-1} \frac{L}{mol\cdot min})[\mathrm{IO_3^-}]^1[\mathrm{H_2SeO_3}]^0\] Or simply as: \[Rate = 2 \times 10^{-1}[\mathrm{IO_3^-}]\] So, the rate law is \(Rate = 2 \times 10^{-1}[\mathrm{IO_3^-}]\) and the value of the rate constant is \(2 \times 10^{-1} \frac{L}{mol\cdot min}\).

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Chemical Kinetics
Chemical kinetics focuses on understanding the speed or rate at which a chemical reaction occurs. It tells us how swiftly reactants are transformed into products, offering insights into the reaction mechanisms. When we study chemical kinetics, we often determine a rate law, like in the exercise given. The rate law provides a mathematical description of how the reaction rate depends on the concentration of reactants.
  • Reaction rates are generally measured in terms of concentration changes over time, like moles per liter per second or minute.
  • Kinetics can help us predict how a reaction will proceed under different conditions.
  • It also offers clues about which reactants have the greatest impact on the rate of reaction.
Studying kinetics is crucial in fields like pharmaceuticals, where precise reaction control can impact drug production and effectiveness. Understanding kinetics can also help in environmental chemistry, aiding in the design of more effective chemical processes to reduce pollutants.
Reaction Order
Reaction order explains how the rate of a chemical reaction is affected by the concentration of reactants. It is usually expressed in the rate law as an exponent associated with each reactant concentration. In the given exercise, understanding the reaction order is key to figuring out the rate law.Here's a breakdown of reaction order:
  • First-order reactions: The rate changes linearly with the concentration of a single reactant. If the concentration doubles, the rate doubles.
  • Zero-order reactions: The rate is independent of the concentration of a reactant. No matter how much the concentration changes, the rate stays the same.
In the step-by-step solution, the reaction was determined to be first-order with respect to \[\mathrm{IO_3^-}\], and zero-order with respect to \[\mathrm{H_2SeO_3}\]. This decision was made by observing changes in the reaction rate when altering the concentrations.
Rate Constant
The rate constant, symbolized by \(k\), is a crucial element in the rate law. It is a coefficient reflecting the speed of a reaction, and it varies with conditions such as temperature. A rate constant links the reaction rate to the concentration of reactants through the rate law expression.
  • The value of \(k\) is derived by inserting known values of concentration and rate into the rate law formula.
  • The units of \(k\) vary depending on the overall order of the reaction.
  • For a first-order reaction, \(k\) has units of \( ext{time}^{-1}\), while for a second-order reaction, \(k\) has units of \(\text{L/mol}\cdot\text{time}\).
In the provided exercise, the rate constant was calculated using the equation \[4.0\times 10^{-4} = k(2.0\times10^{-3})\]resulting in \(k\) equaling \[2 \times 10^{-1} \text{ L/mol}\cdot\text{min}.\]This illustrates how the rate constant connects the reaction rate to the concentration of \[\mathrm{IO_3^-}\], helping us understand the kinetic behavior of the reaction.

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Most popular questions from this chapter

Consider the general reaction $$ \mathrm{aA}+\mathrm{bB} \longrightarrow \mathrm{cC} $$ and the following average rate data over some time period \(\Delta t :\) $$ \begin{aligned}-\frac{\Delta \mathrm{A}}{\Delta t} &=0.0080 \mathrm{mol} / \mathrm{L} \cdot \mathrm{s} \\\\-& \frac{\Delta \mathrm{B}}{\Delta t}=0.0120 \mathrm{mol} / \mathrm{L} \cdot \mathrm{s} \\ \frac{\Delta \mathrm{C}}{\Delta t} &=0.0160 \mathrm{mol} / \mathrm{L} \cdot \mathrm{s} \end{aligned} $$ Determine a set of possible coefficients to balance this general reaction.

Assuming that the mechanism for the hydrogenation of \(\mathrm{C}_{2} \mathrm{H}_{4}\) given in Section 12.7 is correct, would you predict that the product of the reaction of \(\mathrm{C}_{2} \mathrm{H}_{4}\) with \(\mathrm{D}_{2}\) would be \(\mathrm{CH}_{2} \mathrm{D}-\mathrm{CH}_{2} \mathrm{D}\) or \(\mathrm{CHD}_{2}-\mathrm{CH}_{3} ?\) How could the reaction of \(\mathrm{C}_{2} \mathrm{H}_{4}\) with \(\mathrm{D}_{2}\) be used to confirm the mechanism for the hydrogenation of \(\mathrm{C}_{2} \mathrm{H}_{4}\) given in Section 12.7\(?\)

Rate Laws from Experimental Data: Initial Rates Method. The reaction $$2 \mathrm{NO}(g)+\mathrm{Cl}_{2}(g) \longrightarrow 2 \mathrm{NOCl}(g)$$ was studied at \(-10^{\circ} \mathrm{C}\). The following results were obtained where $$\text { Rate }=-\frac{\Delta\left[\mathrm{Cl}_{2}\right]}{\Delta t}$$ $$ \begin{array}{ccc} {[\mathrm{NO}]_{0}} & {\left[\mathrm{Cl}_{2}\right]_{0}} & \text { Initial Rate } \\ (\mathrm{mol} / \mathrm{L}) & (\mathrm{mol} / \mathrm{L}) & (\mathrm{mol} / \mathrm{L} \cdot \mathrm{min}) \\ 0.10 & 0.10 & 0.18 \\ 0.10 & 0.20 & 0.36 \\ 0.20 & 0.20 & 1.45 \end{array} $$ a. What is the rate law? b. What is the value of the rate constant?

A popular chemical demonstration is the "magic genie" procedure, in which hydrogen peroxide decomposes to water and oxygen gas with the aid of a catalyst. The activation energy of this (uncatalyzed) reaction is 70.0 \(\mathrm{kJ} / \mathrm{mol}\) . When the catalyst is added, the activation energy (at \(20 .^{\circ} \mathrm{C} )\) is 42.0 \(\mathrm{kJ} / \mathrm{mol}\) . Theoretically, to what temperature ( \((\mathrm{C})\) would one have to heat the hydrogen peroxide solution so that the rate of the uncatalyzed reaction is equal to the rate of the catalyzed reaction at \(20 .^{\circ} \mathrm{C} ?\) Assume the frequency factor \(A\) is constant, and assume the initial concentrations are the same.

A certain reaction has the following general form: $$ \mathrm{aA} \longrightarrow \mathrm{bB} $$ At a particular temperature and \([\mathrm{A}]_{0}=2.00 \times 10^{-2} M,\) con- centration versus time data were collected for this reaction, and a plot of \(\ln [\mathrm{A}]\) versus time resulted in a straight line with a slope value of \(-2.97 \times 10^{-2} \mathrm{min}^{-1}\) . a. Determine the rate law, the integrated rate law, and the value of the rate constant for this reaction. b. Calculate the half-life for this reaction. c. How much time is required for the concentration of A to decrease to \(2.50 \times 10^{-3} M ?\)

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