For the isothermal expansion of a gas into a vacuum, \(\Delta E=0, q=0,\) and \(w=0 .\) (a) Is this a spontaneous process? (b) Explain why no work is done by the system during this process. (c) What is the "driving force" for the expansion of the gas: enthalpy or entropy?

Short Answer

Expert verified
(a) Yes, the process is spontaneous because the change in entropy (\(\Delta S\)) is positive, resulting in a negative change in Gibbs Free Energy (\(\Delta G < 0\)). (b) No work is done during this process because the external pressure (\(P_{ext}\)) is zero, as the gas is expanding into a vacuum. Therefore, the work done (\(w\)) is also zero. (c) The driving force for the expansion of the gas is entropy, as the enthalpy (\(\Delta H\)) remains constant (equal to zero) during the isothermal process, while the entropy (\(\Delta S\)) increases.

Step by step solution

01

(a) Evaluate the spontaneity of the process

To determine if a process is spontaneous, we need to consider the change in Gibbs free energy, which is given by the following equation: \(\Delta G = \Delta H - T \Delta S\) where \(\Delta G\) is the change in Gibbs free energy, \(\Delta H\) is the change in enthalpy, \(T\) is the temperature, and \(\Delta S\) is the change in entropy. A process is considered spontaneous if \(\Delta G < 0\). In the given problem, since the process is isothermal, we can re-write the equation as: \(\Delta G = q + w - T \Delta S\) We are given that \(q = 0\) and \(w = 0\), so the equation simplifies to: \(\Delta G = - T \Delta S\) If \(\Delta S > 0\), the process will be spontaneous since \(\Delta G\) will be less than zero. An expansion of a gas results in an increase in entropy because the particles of the gas have more space to move around, which means \(\Delta S > 0\). Thus, the process is spontaneous.
02

(b) Explain why no work is done during the process

During the isothermal expansion of a gas into a vacuum, the gas expands freely with no pressure exerted externally (since it is in a vacuum). Work is defined as the energy transferred due to the force acting on an object over a certain distance, and in this case, the force would be exerted by the pressure of the gas. The formula for work done in a thermodynamic system involving a gas is given by: \(w = - \int_{V_1}^{V_2} P_{ext} dV\) where \(w\) is the work done by the gas, \(V_1\) and \(V_2\) are the initial and final volumes of the gas, and \(P_{ext}\) is the external pressure. In this case, since the gas is expanding into a vacuum, \(P_{ext} = 0\), and hence, the work done is equal to \(0\).
03

(c) Identify the driving force for expansion: enthalpy or entropy

In order to determine the driving force for the expansion of the gas, we need to consider whether the change in enthalpy (\(\Delta H\)) or the change in entropy (\(\Delta S\)) is the dominant factor in the Gibbs free energy equation (\(\Delta G = \Delta H - T \Delta S\)). Since the process is isothermal, \(\Delta E = 0\), and the internal energy of a gas depends only on its temperature, the enthalpy of the gas also remains constant during the expansion process because \(\Delta H = \Delta E + P_\Delta V\). Therefore, \(\Delta H = 0\). On the other hand, as mentioned earlier, the entropy of the gas increases during expansion, which means \(\Delta S > 0\). Since \(\Delta H = 0\) and \(\Delta S > 0\), the driving force for the gas expansion is the entropy change. The expansion of the gas results in an increase in disorder or randomness in the system, which is consistent with an increase in entropy.

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!

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

Consider the following three reactions: $$ \begin{array}{l}{\text { (i) } \operatorname{Ti}(s)+2 \mathrm{Cl}_{2}(g) \longrightarrow \operatorname{TiCl}_{4}(g)} \\ {\text { (ii) } \mathrm{C}_{2} \mathrm{H}_{6}(g)+7 \mathrm{Cl}_{2}(g) \longrightarrow 2 \mathrm{CCl}_{4}(g)+6 \mathrm{HCl}(g)} \\ {\text { (iii) } \mathrm{BaO}(s)+\mathrm{CO}_{2}(g) \longrightarrow \mathrm{BaCO}_{3}(s)}\end{array} $$ (a) For each of the reactions, use data in Appendix \(C\) to calculate \(\Delta H^{\circ}, \Delta G^{\circ}, K,\) and \(\Delta S^{\circ}\) at \(25^{\circ} \mathrm{C}\) . (b) Which of these reactions are spontaneous under standard conditions at \(25^{\circ} \mathrm{C} ?(\mathbf{c})\) For each of the reactions, predict the manner in which the change in free energy varies with an increase in temperature.

A system goes from state 1 to state 2 and back to state \(1 .\) (a) Is \(\Delta E\) the same in magnitude for both the forward and reverse processes? (b) Without further information, can you conclude that the amount of heat transferred to the system as it goes from state 1 to state 2 is the same or different as compared to that upon going from state 2 back to state 1\(?(\mathbf{c})\) Suppose the changes in state are reversible processes. Is the work done by the system upon going from state 1 to state 2 the same or different as compared to that upon going from state 2 back to state 1\(?\)

(a) For a process that occurs at constant temperature, does the change in Gibbs free energy depend on changes in the enthalpy and entropy of the system? (b) For a certain process that occurs at constant \(T\) and \(P\) , the value of \(\Delta G\) is positive. Is the process spontaneous? (c) If \(\Delta G\) for a process is large, is the rate at which it occurs fast?

In each of the following pairs, which compound would you expect to have the higher standard molar entropy: (a) \(\mathrm{C}_{2} \mathrm{H}_{2}(g)\) or \(\mathrm{C}_{2} \mathrm{H}_{6}(g),(\mathbf{b}) \mathrm{CO}_{2}(g)\) or \(\mathrm{CO}(g) ?\)

The value of \(K_{a}\) for nitrous acid \(\left(\mathrm{HNO}_{2}\right)\) at \(25^{\circ} \mathrm{C}\) is given in Appendix D. (a) Write the chemical equation for the equilibrium that corresponds to \(K_{a \cdot}\) (b) By using the value of \(K_{a},\) calculate \(\Delta G^{\circ}\) for the dissociation of nitrous acid in aqueous solution. (c) What is the value of \(\Delta G\) at equilibrium? (d) What is the value of \(\Delta G\) when \(\left[\mathrm{H}^{+}\right]=5.0 \times 10^{-2} M\) \(\left[\mathrm{NO}_{2}^{-}\right]=6.0 \times 10^{-4} M,\) and \(\left[\mathrm{HNO}_{2}\right]=0.20 \mathrm{M} ?\)

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