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What are the units for each of the following if the concentrations are expressed in moles per liter and the time in seconds? a. rate of a chemical reaction b. rate constant for a zero-order rate law c. rate constant for a first-order rate law d. rate constant for a second-order rate law e. rate constant for a third-order rate law

Short Answer

Expert verified
a. The units of the rate of a chemical reaction are M/s. b. The units of the rate constant for a zero-order rate law are M/s. c. The units of the rate constant for a first-order rate law are \(s^{-1}\). d. The units of the rate constant for a second-order rate law are \(L * \text{mol}^{-1} * \text{s}^{-1}\). e. The units of the rate constant for a third-order rate law are \(L^2 * \text{mol}^{-2} * \text{s}^{-1}\).

Step by step solution

01

Identify the rate of a chemical reaction

The rate of a chemical reaction is defined as the change in concentration of one of the reactants or products over a change in time. Mathematically, we can write the rate as: \(\text{rate} = -\frac{1}{\Delta t} \Delta [A]\) or \(\frac{1}{\Delta t} \Delta [B]\), where \([A]\) and \([B]\) represent the concentrations of the reactants.
02

Determine the units

Given the concentration is provided in moles per liter (M) and time in seconds (s), the rate will have the units of M/s. #b-e. Units of Rate Constants for different order rate laws#
03

Using the general rate law equation

The general rate law equation is given by: rate = k * [A]^m * [B]^n, where k is the rate constant, [A] and [B] are concentrations of reactants, and m and n are the orders of the reaction concerning the reactants.
04

Calculate the rate constant units for different orders

b. For a zero-order rate law (\(m+n=0\)), the rate law equation becomes: rate = k. So the rate constant units will be the same as the rate, which is M/s. c. For a first-order rate law (\(m+n=1\)), the rate law equation becomes: rate = k * [A]. Thus, the rate constant units are \(\frac{\text{M}}{\text{s} * \text{M}}\), which simplifies to \(s^{-1}\). d. For a second-order rate law (\(m+n=2\)), the rate law equation becomes: rate = k * [A]^2 or rate = k * [A] * [B]. In this case, the rate constant units are \(\frac{\text{M}}{\text{s} * \text{M}^2}\), which simplifies to \(L * \text{mol}^{-1} * \text{s}^{-1}\). e. For a third-order rate law (\(m+n=3\)), the rate law equation becomes rate = k * [A]^3 or rate = k * [A]^2 * [B]. In this case, the rate constant units are \(\frac{\text{M}}{\text{s} * \text{M}^3}\), which simplifies to \(L^2 * \text{mol}^{-2} * \text{s}^{-1}\).

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Key Concepts

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

Chemical Reaction Rates
Understanding the rate of a chemical reaction is central to the study of chemical kinetics. This concept refers to how fast a reactant is used up or how fast a product forms in a chemical reaction. It's usually expressed as a change in concentration over time. For example, if the concentration of a reactant decreases over time, then the rate at which the reaction occurs is calculated based on this change. A general expression for this rate is:
\[\text{rate} = -\frac{1}{\Delta t}\Delta [A]\]
or
\[\text{rate} = \frac{1}{\Delta t}\Delta [B]\]
where \([A]\) and \([B]\) are the concentrations of the reactants, and \(\Delta\) signifies the change over time \(\Delta t\). In simpler terms, the negative sign is usually used when we are looking at the disappearance of a reactant, and we ignore it when we describe the formation of a product. We measure the rate in moles per liter per second (M/s), providing us insight into the dynamics of the chemical process.
Zero-Order Rate Law
The zero-order rate law describes a reaction where the rate is independent of the concentration of the reactant(s). This scenario might seem counterintuitive because we might expect that having more reactant molecules would lead to a faster reaction. However, in some cases, such as when a catalyst surface is fully saturated with reactant molecules, additional increases in concentration don't affect the rate. When we write the rate equation as
\[\text{rate} = k\]
for a zero-order reaction, \(k\) is the rate constant, which has units of M/s. This simplifies the understanding of the mechanism because the rate will always be constant as long as we have some reactant present. It's important to remember that these reactions will stop once the reactant is used up, as opposed to merely slowing down as the reactants are depleted.
First-Order Rate Law
In first-order reactions, the rate is directly proportional to the concentration of a single reactant. This is commonly observed in many natural and industrial processes, including radioactive decay and certain organic reactions. The rate law for a first-order reaction looks like this:
\[\text{rate} = k[A]\]
where \([A]\) is the concentration of the reactant and \(k\) is the rate constant. The units of the rate constant for first-order reactions are inverse seconds \(s^{-1}\), which signal that the rate will halve for every halving in the concentration of the reactant. This kind of behaviour is often advantageous to understand and predict how a single reactant can control the speed of a reaction.
Second-Order Rate Law
Second-order reactions are characterized by the reaction rate being proportional to the square of a reactant's concentration or the product of two reactants' concentrations. These reactions are described by the rate law
\[\text{rate} = k[A]^2\]
or alternatively
\[\text{rate} = k[A][B]\]
in cases where two different reactants are involved. The rate constant \(k\) has units of \(L \cdot \text{mol}^{-1} \cdot \text{s}^{-1}\), indicating that the reaction rate increases quadratically with an increase in concentration of a single reactant or linearly with the concentration of two reactants. Analyzing such reactions often requires careful consideration of how concentrations interact with each other to affect the reaction speed.
Third-Order Rate Law
A third-order reaction involves either the cubic dependence on the concentration of a single reactant or a combination where the rate is proportional to the product of three reactant concentrations. These cases are exemplified by:
\[\text{rate} = k[A]^3\]
or
\[\text{rate} = k[A]^2[B]\]
or any other combination where the sum of the powers equals three. The rate constant \(k\) in third-order reactions has units of \(L^2 \cdot \text{mol}^{-2} \cdot \text{s}^{-1}\). Due to the high order, even small changes in reactant concentration can lead to large changes in the reaction rate, making these reactions sensitive to concentration variations. Understanding third-order reactions is often necessary for complex chemical processes where multiple reactants are involved.

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Most popular questions from this chapter

A certain reaction has the following general form: $$\text { aA } \longrightarrow \mathrm{bB}$$ At a particular temperature and \([\mathrm{A}]_{0}=2.00 \times 10^{-2} \mathrm{M}, \)concentration 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 \(2.50 \times 10^{-3} \mathrm{M} ?\)

Table \(11-2\) illustrates how the average rate of a reaction decreases with time. Why does the average rate decrease with time? How does the instantaneous rate of a reaction depend on time? Why are initial rates used by convention?

One of the concerns about the use of Freons is that they will migrate to the upper atmosphere, where chlorine atoms can be generated by the following reaction: $$\mathrm{CCl}_{2} \mathrm{F}_{2}(g) \stackrel{h v}{\longrightarrow} \mathrm{CF}_{2} \mathrm{Cl}(g)+\mathrm{Cl}(g)$$ Chlorine atoms can act as a catalyst for the destruction of ozone. The activation energy for the reaction $$\mathrm{Cl}(g)+\mathrm{O}_{3}(g) \longrightarrow \mathrm{ClO}(g)+\mathrm{O}_{2}(g)$$is \(2.1 \mathrm{kJ} / \mathrm{mol} .\) Which is the more effective catalyst for the destruction of ozone, Cl or NO? (See Exercise 75.)

Chemists commonly use a rule of thumb that an increase of \(10 \space\mathrm{K}\) in temperature doubles the rate of a reaction. What must the activation energy be for this statement to be true for a temperature increase from 25 to \(35^{\circ} \mathrm{C} ?\)

The rate law for a reaction can be determined only from experiment and not from the balanced equation. Two experimental procedures were outlined in Chapter \(11 .\) What are these two procedures? Explain how each method is used to determine rate laws.

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