Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

The rate constant for the forward reaction: \(\mathrm{A}(\mathrm{g}) \rightleftharpoons 2 \mathrm{~B}(\mathrm{~g})\) is \(1.5 \times 10^{-3} \mathrm{~s}^{-1}\) at \(300 \mathrm{~K}\). If \(10^{-5}\) moles of 'A' and 100 moles of ' \(\mathrm{B}\) ' are present in a 10 litre vessel at equilibrium, then the rate constant of the backward reaction at this temperature is (a) \(1.5 \times 10^{-3} \mathrm{M}^{-1} \mathrm{~s}^{-1}\) (b) \(1.5 \times 10^{-1} \mathrm{M}^{-1} \mathrm{~s}^{-1}\) (c) \(1.5 \times 10^{-11} \mathrm{M}^{-1} \mathrm{~s}^{-1}\) (d) \(1.5 \times 10^{-12} \mathrm{M}^{-1} \mathrm{~s}^{-1}\)

Short Answer

Expert verified
The rate constant of the backward reaction at this temperature is \(1.5 \times 10^{-11} \mathrm{M}^{-1} \mathrm{~s}^{-1}\), which corresponds to option (c).

Step by step solution

01

Write the Equilibrium Expression

The equilibrium expression for the reversible reaction \(\mathrm{A}(\mathrm{g}) \rightleftharpoons 2 \mathrm{B}(\mathrm{g})\) is given by the equilibrium constant \(K_c = \frac{[\mathrm{B}]^2}{[\mathrm{A}]}\), where [\mathrm{A}] and [\mathrm{B}] are the molar concentrations of A and B at equilibrium.
02

Calculate the Molar Concentrations at Equilibrium

Calculate the molar concentrations using the number of moles and volume of the vessel. For A: \[ [\mathrm{A}] = \frac{10^{-5}\ \text{moles}}{10\ \text{L}} = 10^{-6}\ \text{M} \] For B: \[ [\mathrm{B}] = \frac{100\ \text{moles}}{10\ \text{L}} = 10\ \text{M} \]
03

Calculate the Equilibrium Constant \(K_c\)

Using the forward reaction rate constant (\(k_f\)) and the molar concentrations: \(K_c = \frac{k_f}{k_b}\) where \(k_b\) is the backward reaction rate constant. Since \(k_f\) is given and Kc can be calculated from the equilibrium concentrations, we can find \(k_b\).
04

Calculate the Equilibrium Constant \(K_c\) Using Concentrations

Substitute the calculated concentrations into the equilibrium expression: \[ K_c = \frac{[\mathrm{B}]^2}{[\mathrm{A}]} = \frac{(10)^2}{10^{-6}} = \frac{100}{10^{-6}} = 10^8 \]
05

Solve for the Backward Reaction Rate Constant \(k_b\)

Rearrange the equation \(K_c = \frac{k_f}{k_b}\) to solve for \(k_b\): \[ k_b = \frac{k_f}{K_c} = \frac{1.5 \times 10^{-3}\ \text{s}^{-1}}{10^8} = 1.5 \times 10^{-11}\ \text{M}^{-1}\text{s}^{-1} \] This matches answer option (c).

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

Key Concepts

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

Understanding Chemical Equilibrium
In chemistry, chemical equilibrium is a state in which the rate of the forward reaction equals the rate of the backward reaction, meaning that the concentrations of reactants and products remain constant over time. This does not imply that the reactants and products are in equal concentrations, but rather that their ratios are stable. It's important to understand that equilibrium is dynamic; molecules continue to react, but there's no net change in concentration.

Think of it like a busy street where the number of cars entering equals the number of cars leaving, so the total number of cars on the street stays the same. In the context of the exercise, equilibrium involves the gas A transforming into gas B and vice versa. When the system has reached equilibrium, we can quantify the position of this equilibrium in terms of the equilibrium constant, \(K_c\), which compares the concentration of the products raised to the power of their coefficients to the concentration of the reactants raised to the power of their coefficients.
Rate Constant and its Role in Reactions
The rate constant, denoted as \(k\), is a crucial parameter in chemical kinetics, offering insight into the speed of a reaction. It is independent of the concentration of reactants but varies with temperature and the presence of a catalyst. In a given reaction, the rate constant for the forward reaction \(k_f\), and the backward reaction \(k_b\), are generally not equal and are reflective of how quickly products form and revert to reactants, respectively.

For instance, the exercise presents us with a scenario where the forward rate constant \(1.5 \times 10^{-3} \text{s}^{-1}\) is given, and we must infer the backward rate constant using the equilibrium concentrations. It's similar to knowing how fast a pendulum swings in one direction and using that information, along with the equilibrium point, to determine how fast it swings back.
Reaction Kinetics Fundamentals
Reaction kinetics is the field that studies the rates of chemical reactions and the factors that affect these rates. It tells us not just how long a reaction will take to reach equilibrium, but also how the presence of different substances or changes in conditions like temperature can speed up or slow down this process. Kinetics is central to understanding reaction mechanisms—the steps that take place during a reaction.

Effects of Concentration and Temperature

For example, increasing the concentration of reactants typically increases the rate of reaction because there are more particles to collide and react. Temperature also plays a key role; as it increases, particles move faster, leading to more frequent and energetic collisions, thus increasing the rate of reaction. In the given exercise, the reaction kinetics principles allow us to determine the backward reaction rate constant by understanding the relationship between the equilibrium constant and the forward reaction rate constant.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

When \(\alpha\) -D-glucose is dissolved in water, it undergoes a partial conversion to \beta-D-glucose. This conversion, called mutarotation, stops when \(64.0 \%\) of the glucose is in the \(\beta\) -form. Assuming that equilibrium has been attained, what is \(\Delta G^{\circ}\) for the reaction: \(\alpha\) -D-glucose \(\rightleftharpoons \beta-\mathrm{D}\) glucose, at this experimental temperature? (a) \(-R T \log _{10}(1.6)\) (b) \(-R T \log _{10}(1.78)\) (c) \(-R T \log _{e}(1.78)\) (d) \(-R T \log _{e}(1.6)\)

\(\mathrm{I}_{2}+\mathrm{I}^{-} \rightleftharpoons \mathrm{I}_{3}^{-} .\) This reaction is set up in aqueous medium. We start with \(1 \mathrm{~mol}\) of \(\mathrm{I}\), and \(0.5 \mathrm{~mol}\) of \(\mathrm{I}^{-}\) in \(1 \mathrm{~L}\) flask. After equilibrium is reached, excess of \(\mathrm{AgNO}_{3}\) gave \(0.25 \mathrm{~mol}\) of yellow precipitate. Equilibrium constant is (a) \(1.33\) (b) \(2.66\) (c) \(0.375\) (d) \(0.75\)

What is the approximate value of \(\log K_{\mathrm{p}}\) for the reaction: \(\mathrm{N}_{2}(\mathrm{~g})+3 \mathrm{H}_{2}(\mathrm{~g}) \rightleftharpoons 2 \mathrm{NH}_{3}(\mathrm{~g})\) at \(25^{\circ} \mathrm{C}\) The standard enthalpy of formation of \(\mathrm{NH}_{3}(\mathrm{~g})\) is \(-40.0 \mathrm{~kJ} / \mathrm{mol}\) and standard entropies of \(\mathrm{N}_{2}(\mathrm{~g}), \mathrm{H}_{2}(\mathrm{~g})\) and \(\mathrm{NH}_{3}(\mathrm{~g})\) are 191,130 and \(192 \mathrm{JK}^{-1} \mathrm{~mol}^{-1}\), respectively. (a) \(0.04\) (b) \(7.05\) (c) \(8.6\) (d) \(3.73\)

Amounts of \(0.8 \mathrm{~mol}\) of \(\mathrm{PCl}_{5}\) and \(0.2\) mole of \(\mathrm{PCl}_{3}\) are mixed in a \(1 \mathrm{i}\) flask. At equilibrium, \(0.4\) mole of \(\mathrm{PCl}_{3}\) is present. The equilibrium constant for the reaction, \(\mathrm{PCl}_{5}(\mathrm{~g}) \rightleftharpoons \mathrm{PCl}_{3}(\mathrm{~g})+\mathrm{Cl}_{2}(\mathrm{~g})\) will be (a) \(0.05 \mathrm{~mol}^{-1}\) (b) \(0.13 \mathrm{~mol} 1^{-1}\) (c) \(0.013 \mathrm{~mol} 1^{-1}\) (d) \(0.60 \mathrm{~mol} 1^{-1}\)

Reaction: \(\mathrm{A}(\mathrm{g})+\mathrm{B}(\mathrm{g}) \rightleftharpoons \mathrm{C}(\mathrm{g})\) \(+\mathrm{D}(\mathrm{g})\), occurs in a single step. The rate constant of forward reaction is \(2.0 \times 10^{-3} \mathrm{~mol}^{-1} \mathrm{~L} \mathrm{~s}^{-1} .\) When the reaction is started with equimolar amounts of \(\mathrm{A}\) and \(\mathrm{B}\), it is found that the concentration of \(\mathrm{A}\) is twice that of \(\mathrm{C}\) at equilibrium. The rate constant of the backward reaction is (a) \(5.0 \times 10^{-4} \mathrm{~mol}^{-1} \mathrm{~L} \mathrm{~s}^{-1}\) (b) \(8.0 \times 10^{-3} \mathrm{~mol}^{-1} \mathrm{~L} \mathrm{~s}^{-1}\) (c) \(1.25 \times 10^{2} \mathrm{~mol}^{-1} \mathrm{~L} \mathrm{~s}^{-1}\) (d) \(2.0 \times 10^{3} \mathrm{~mol}^{-1} \mathrm{~L} \mathrm{~s}^{-1}\)

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free