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

For the reaction \(\mathrm{H}_{2}(\mathrm{~g})+\frac{1}{2} \mathrm{O}_{2}(\mathrm{~g}) \longrightarrow \mathrm{H}_{2} \mathrm{O}(1)\), the value of \(\Delta \mathrm{H}=-285.8 \mathrm{~kJ} \mathrm{~mol}^{-1}\) and \(\Delta \mathrm{S}=0.163\) \(\mathrm{JK}^{-1} \mathrm{~mol}^{-1}\). The free energy change at \(300 \mathrm{~K}\). for the reaction, is: (a) \(-289.6 \mathrm{~kJ} \mathrm{~mol}^{-1}\) (b) \(437.5 \mathrm{~kJ} \mathrm{~mol}^{-1}\) (c) \(-334.7 \mathrm{~kJ} \mathrm{~mol}^{-1}\) (d) \(-291.6 \mathrm{~kJ} \mathrm{~mol}^{-1}\)

Short Answer

Expert verified
The free energy change is closest to -289.6 kJ/mol, so the answer is (a).

Step by step solution

01

Identify the Formula

We need the formula for calculating the Gibbs free energy change \( \Delta G \). The formula is given by:\[ \Delta G = \Delta H - T \Delta S \] where \( \Delta G \) is the change in free energy, \( \Delta H \) is the enthalpy change, \( T \) is the temperature in Kelvin, and \( \Delta S \) is the entropy change.
02

Substitute Known Values

We are given \( \Delta H = -285.8 \ \mathrm{kJ \ mol}^{-1} \), \( \Delta S = 0.163 \ \mathrm{J \ K}^{-1} \mathrm{~mol}^{-1} \), and \( T = 300 \ \mathrm{K} \). First, we need to convert \( \Delta S \) from \( \mathrm{J} \) to \( \mathrm{kJ} \) to match the units of \( \Delta H \). \[ \Delta S = 0.163 \ \mathrm{J \ K}^{-1} \mathrm{~mol}^{-1} = 0.000163 \ \mathrm{kJ \ K}^{-1} \mathrm{~mol}^{-1} \]Now substitute these values into the formula:\[\Delta G = -285.8 - (300 \times 0.000163)\]
03

Perform the Calculation

Calculate the term \( T \Delta S \):\[ 300 \times 0.000163 = 0.0489 \ \mathrm{kJ \ mol}^{-1} \]Now compute \( \Delta G \):\[ \Delta G = -285.8 - 0.0489 = -285.8489 \ \mathrm{kJ \ mol}^{-1} \]
04

Select the Closest Answer

The calculated \( \Delta G \) is \(-285.8489 \ \mathrm{kJ \ mol}^{-1} \), which is closest to option (a) \(-289.6 \ \mathrm{kJ \ mol}^{-1}\). Therefore, the correct answer is:(a) \(-289.6 \ \mathrm{kJ \ mol}^{-1}\).

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.

Enthalpy Change
Understanding enthalpy change is crucial in thermodynamics. Enthalpy change, denoted as \(\Delta H\), represents the heat absorbed or released during a chemical reaction at constant pressure. It helps in determining whether a reaction is exothermic or endothermic.
For exothermic reactions, \(\Delta H\) is negative as the system releases heat to the surroundings. For the given reaction of hydrogen gas with oxygen to form water, \(\Delta H\) is \(-285.8 \ \, \mathrm{kJ \ mol}^{-1}\), indicating an exothermic process. This means energy is released, making the environment around the reaction warm.
Knowing the sign and magnitude of \(\Delta H\) helps in predicting how the reaction will affect its surroundings. Positive values denote that heat is absorbed, categorizing it as an endothermic reaction. Understanding enthalpy provides insight into energy changes in chemical systems.
Entropy Change
Entropy change, represented as \(\Delta S\), is a measure of disorder or randomness in a system. In thermodynamics, understanding entropy helps predict the spontaneity of a process.
In our exercise, the entropy change is \(0.163 \, \mathrm{J \ K}^{-1} \mathrm{~mol}^{-1}\). This indicates a slight increase in disorder as the reaction proceeds from reactants to products. Entropy is a crucial factor when calculating Gibbs free energy.
  • Positive \(\Delta S\) implies that the disorder increases, which tends to favor spontaneous reactions.
  • Negative \(\Delta S\) implies a decrease in disorder, usually making the process non-spontaneous unless driven by other factors like enthalpy change.
Understanding entropy is essential for predicting how changes in temperature and pressure will influence the favorability of reactions.
Thermodynamics in Chemistry
Thermodynamics in chemistry involves studying energy changes and the physical properties of matter during chemical reactions and physical transformations.
The Gibbs free energy, \(\Delta G\), combines enthalpy and entropy to predict the spontaneity of a reaction. It is calculated with the formula: \[ \Delta G = \Delta H - T \Delta S \] where \(T\) is the temperature measured in Kelvin.
A negative \(\Delta G\) suggests that a reaction is spontaneous, meaning it can proceed without any external energy input. In the given exercise, calculation shows \(\Delta G = -285.8489 \, \mathrm{kJ \ mol}^{-1}\), meaning the reaction is spontaneous.
  • If \(\Delta G\) is zero, the system is at equilibrium, and no net change occurs.
  • A positive \(\Delta G\) indicates a non-spontaneous reaction, requiring energy input to proceed.
Overall, thermodynamics in chemistry helps chemists understand and predict the direction and extent of chemical reactions.

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

In monoatomic gases, ratio of specific heat at constant pressure to that at constant volume is: (a) \(3 / 5\) (b) \(5 / 3\) (c) \(7 / 5\) (d) \(4 / 5\)

The change in entropy, in the conversion of one mole of water at \(373 \mathrm{~K}\) to vapour at the same temperature is (Latent heat of vaporization of water \(=2.257 \mathrm{~kJ} \mathrm{~g}^{-1}\) ) (a) \(99 \mathrm{JK}^{-1}\) (b) \(129 \mathrm{JK}^{-1}\) (c) \(89 \mathrm{JK}^{-1}\) (d) \(109 \mathrm{JK}^{-1}\)

Standard state Gibbs free energy change for isomerization reaction, cis-2-pentene \(\rightleftharpoons\) trans-2-pentene is \(-3.67 \mathrm{~kJ} / \mathrm{mol}\) at \(400 \mathrm{~K}\). if more trans- 2 -pentene is added to the reaction vessel, then: (a) More cis-2-pentene is formed (b) Additional trans-2-pentene is formed (c) Equilibrium remains unaffected (d) Equilibrium is shifted in the forward direction

If the standard entropies of \(\mathrm{CH}_{4}(\mathrm{~g}), \mathrm{H}_{2} \mathrm{O}(\mathrm{g}), \mathrm{CO}_{2}(\mathrm{~g})\) and \(\mathrm{H}_{2}(\mathrm{~g})\) are \(186.2,188.2,197.6\) and \(130.6 \mathrm{JK}^{-1}\) \(\mathrm{mol}^{-1}\) respectively, then the standard entropy change for the reaction: \(\mathrm{CH}_{4}(\mathrm{~g})+\mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \longrightarrow \mathrm{CO}_{2}(\mathrm{~g})+3 \mathrm{H}_{2}(\mathrm{~g})\) is: (a) \(215 \mathrm{JK}^{-1} \mathrm{~mol}^{-1}\) (b) \(225 \mathrm{JK}^{-1} \mathrm{~mol}^{-1}\) (c) \(145 \mathrm{JK}^{-1} \mathrm{~mol}^{-1}\) (d) \(285 \mathrm{JK}^{-1} \mathrm{~mol}^{-1}\)

Which of the following is not an endothermic reaction? (a) Combustion of methane (b) Decomposition of water (c) Dehydrogenation of ethane or ethylene (d) Conversion of graphite to diamond

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