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

Is \(\Delta S_{\text {surr }}\) favorable or unfavorable for exothermic reactions? Endothermic reactions? Explain.

Short Answer

Expert verified
For exothermic reactions, \(\Delta S_{\text{surr}}\) is positive, indicating an increase in the entropy of the surroundings, which is considered favorable. On the other hand, for endothermic reactions, \(\Delta S_{\text{surr}}\) is negative, indicating a decrease in the entropy of the surroundings, which is considered unfavorable.

Step by step solution

01

Define entropy

Entropy, represented as \(S\), is a measure of the degree of disorder or randomness in a system. An increase in entropy generally means a higher degree of disorder, while a decrease in entropy indicates a lower degree of disorder.
02

Calculate the change in entropy of the surroundings

For chemical reactions, the change in entropy of the surroundings, denoted as \(\Delta S_{\text{surr}}\), can be calculated using the relation: \begin{equation} \Delta S_{\text{surr}} = - \dfrac{q_{\text{sys}}}{T} \end{equation} where \(q_{\text{sys}}\) is the heat flow of the system, which is positive if the system absorbs heat (endothermic) and negative if the system releases heat (exothermic), and \(T\) is the temperature in Kelvin.
03

Analyze the change in entropy of surroundings for exothermic reactions

In an exothermic reaction, heat is released into the surroundings, so \(q_{\text{sys}}\) is negative. Therefore, when we plug this into the equation: \begin{equation} \Delta S_{\text{surr}} = - \dfrac{-q_{\text{sys}}}{T} \end{equation} Since both the numerator and denominator are positive, \(\Delta S_{\text{surr}}\) will be positive, meaning the entropy of the surroundings increases.
04

Analyze the change in entropy of surroundings for endothermic reactions

In an endothermic reaction, heat is absorbed from the surroundings, so \(q_{\text{sys}}\) is positive. Therefore, when we plug this into the equation: \begin{equation} \Delta S_{\text{surr}} = - \dfrac{q_{\text{sys}}}{T} \end{equation} Since the numerator is positive and the denominator is positive, \(\Delta S_{\text{surr}}\) will be negative, meaning the entropy of the surroundings decreases.
05

Conclude whether the change in entropy of the surroundings is favorable or unfavorable

From the analysis in Steps 3 and 4, we can conclude that: - For exothermic reactions, \(\Delta S_{\text{surr}}\) is positive, which indicates an increase in the entropy of the surroundings. Entropy increasing is generally considered favorable because it leads to a more dispersed and disordered state. - For endothermic reactions, \(\Delta S_{\text{surr}}\) is negative, indicating a decrease in the entropy of the surroundings, which is generally considered unfavorable because it leads to a less dispersed and more ordered state.

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.

Exothermic Reactions
Exothermic reactions are processes where heat is released into the surroundings. This type of reaction is characterized by the system losing energy as it transfers heat to its environment. A classic example of an exothermic reaction is combustion, like burning wood or fossil fuels.

When such reactions occur, the energy emitted increases the thermal energy of the surroundings, which has a direct impact on the entropy of the surroundings. Entropy, a concept in thermodynamics, relates to the level of disorder or randomness. In the case of an exothermic reaction, since the system releases energy (making the heat flow of the system, \(q_{\text{sys}}\), negative), the surroundings absorb this heat.

The change of entropy for the surroundings, \(\Delta S_{\text{surr}}\), is calculated using the formula:
  • \(\Delta S_{\text{surr}} = - \dfrac{q_{\text{sys}}}{T}\)
Here, a negative \(q_{\text{sys}}\) results in a positive change in entropy for the surroundings. This positive increase implies more disorder, which is typically favorable as systems naturally progress towards more random states. Thus, exothermic reactions contribute to increasing the entropy of their environment.
Endothermic Reactions
Endothermic reactions are processes where the system absorbs heat from its surroundings. These reactions require input of energy, which causes the surroundings to become cooler. A good example of an endothermic process is the melting of ice into water.

For these reactions, the heat flow, \(q_{\text{sys}}\), is positive as the system takes in energy. This absorption reduces the thermal energy available in the surroundings, affecting the entropy negatively.
  • The change in entropy of the surroundings for an endothermic reaction is given by:
  • \(\Delta S_{\text{surr}} = - \dfrac{q_{\text{sys}}}{T}\)
Since \(q_{\text{sys}}\) is positive in endothermic reactions, \(\Delta S_{\text{surr}}\) becomes negative. This decrease in entropy is often deemed unfavorable, as it indicates a move towards a more ordered state, contradicting the natural tendency towards disorder. Therefore, endothermic reactions result in a lowering of the entropy of the surroundings.
Entropy Change of Surroundings
The entropy change of the surroundings, represented as \(\Delta S_{\text{surr}}\), plays an essential role in understanding chemical reactions. It measures how the heat exchanged between the system and its environment impacts the latter's disorder or randomness. This value helps in predicting the favorability of reactions based on their thermal interactions with their surroundings.

For both exothermic and endothermic reactions, the entropy change of the surroundings is calculated using the equation:
  • \(\Delta S_{\text{surr}} = - \dfrac{q_{\text{sys}}}{T}\)
This equation reveals that the sign and magnitude of \(\Delta S_{\text{surr}}\) are inversely related to the heat flow of the system.
- In exothermic reactions, where heat is released, \(\Delta S_{\text{surr}}\) is positive, indicating increased disorder.- In endothermic reactions, where heat is absorbed, \(\Delta S_{\text{surr}}\) is negative, pointing to decreased disorder.Understanding whether \(\Delta S_{\text{surr}}\) is favorable or unfavorable is crucial in assessing how these reactions influence the overall entropy change, \(\Delta S_{\text{universe}} = \Delta S_{\text{sys}} + \Delta S_{\text{surr}}\), and therefore their spontaneity and feasibility.

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

Using data from Appendix 4, calculate \(\Delta H^{\circ}, \Delta G^{\circ}\), and \(K(\) at \(298 \mathrm{~K}\) ) for the production of ozone from oxygen: $$ 3 \mathrm{O}_{2}(g) \rightleftharpoons 2 \mathrm{O}_{3}(g) $$ At \(30 \mathrm{~km}\) above the surface of the earth, the temperature is about \(230 . \mathrm{K}\) and the partial pressure of oxygen is about \(1.0 \times 10^{-3}\) atm. Estimate the partial pressure of ozone in equilibrium with oxygen at \(30 \mathrm{~km}\) above the earth's surface. Is it reasonable to assume that the equilibrium between oxygen and ozone is maintained under these conditions? Explain.

The Ostwald process for the commercial production of nitric acid involves three steps: $$ \begin{array}{l} 4 \mathrm{NH}_{3}(g)+5 \mathrm{O}_{2}(g) \underset{825^{\circ} \mathrm{C}}{\longrightarrow} 4 \mathrm{NO}(g)+6 \mathrm{H}_{2} \mathrm{O}(g) \\\ 2 \mathrm{NO}(g)+\mathrm{O}_{2}(g) \longrightarrow 2 \mathrm{NO}_{2}(g) \\ 3 \mathrm{NO}_{2}(g)+\mathrm{H}_{2} \mathrm{O}(l) \longrightarrow 2 \mathrm{HNO}_{3}(l)+\mathrm{NO}(g) \end{array} $$ a. Calculate \(\Delta H^{\circ}, \Delta S^{\circ}, \Delta G^{\circ}\), and \(K\) (at \(\left.298 \mathrm{~K}\right)\) for each of the three steps in the Ostwald process (see Appendix 4). b. Calculate the equilibrium constant for the first step at \(825^{\circ} \mathrm{C}\), assuming \(\Delta H^{\circ}\) and \(\Delta S^{\circ}\) do not depend on temperature. c. Is there a thermodynamic reason for the high temperature in the first step, assuming standard conditions?

The standard free energies of formation and the standard enthalpies of formation at \(298 \mathrm{~K}\) for difluoroacetylene \(\left(\mathrm{C}_{2} \mathrm{~F}_{2}\right)\) and hexafluorobenzene \(\left(\mathrm{C}_{6} \mathrm{~F}_{6}\right)\) are $$ \begin{array}{|lcc|} & \left.\Delta G_{\mathrm{f}}^{\circ}(\mathrm{k}] / \mathrm{mol}\right) & \Delta H_{\mathrm{f}}^{\circ}(\mathrm{kJ} / \mathrm{mol}) \\ \mathrm{C}_{2} \mathrm{~F}_{2}(g) & 191.2 & 241.3 \\ \mathrm{C}_{6} \mathrm{~F}_{6}(g) & 78.2 & 132.8 \\ \hline \end{array} $$ For the following reaction: $$ \mathrm{C}_{6} \mathrm{~F}_{6}(g) \rightleftharpoons 3 \mathrm{C}_{2} \mathrm{~F}_{2}(g) $$ a. calculate \(\Delta S^{\circ}\) at \(298 \mathrm{~K}\). b. calculate \(K\) at \(298 \mathrm{~K}\). c. estimate \(K\) at \(3000 . \mathrm{K}\), assuming \(\Delta H^{\circ}\) and \(\Delta S^{\circ}\) do not depend on temperature.

As \(\mathrm{O}_{2}(l)\) is cooled at \(1 \mathrm{~atm}\), it freezes at \(54.5 \mathrm{~K}\) to form solid \(\mathrm{I}\). At a lower temperature, solid I rearranges to solid II, which has a different crystal structure. Thermal measurements show that \(\Delta H\) for the \(\mathrm{I} \rightarrow\) II phase transition is \(-743.1 \mathrm{~J} / \mathrm{mol}\), and \(\Delta S\) for the same transition is \(-17.0 \mathrm{~J} / \mathrm{K} \cdot\) mol. At what temperature are solids I and II in equilibrium?

List three different ways to calculate the standard free energy change, \(\Delta G^{\circ}\), for a reaction at \(25^{\circ} \mathrm{C}\). How is \(\Delta G^{\circ}\) estimated at temperatures other than \(25^{\circ} \mathrm{C} ?\) What assumptions are made?

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