Calculate standard entropy change in the reaction $$ \mathrm{Fe}_{2} \mathrm{O}_{3}(s)+3 \mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{Fe}(s)+3 \mathrm{H}_{2} \mathrm{O}(l) $$ Given : \(S_{m}^{\circ}\left(\mathrm{Fe}_{2} \mathrm{O}_{3}, \mathrm{~S}\right)=87.4, S_{m}^{\circ}(\mathrm{Fe}, S)=27.3\) \(S_{m}^{\circ}\left(\mathrm{H}_{2}, g\right)=130.7, S_{m}^{\circ}\left(\mathrm{H}_{2} \mathrm{O}, l\right)=69.9 \mathrm{JK}^{-1} \mathrm{~mol}^{-1}\)

Short Answer

Expert verified
-215.2 JK^{-1} mol^{-1}

Step by step solution

01

Write the Reaction

First, write down the reaction for which you need to calculate the standard entropy change: \[ \mathrm{Fe}_{2} \mathrm{O}_{3}(s) + 3 \mathrm{H}_{2}(g) \longrightarrow 2 \mathrm{Fe}(s) + 3 \mathrm{H}_{2} \mathrm{O}(l) \]
02

Apply the Formula for Standard Entropy Change

The standard entropy change (\(\Delta S^\circ\)) for the reaction can be calculated using the formula: \[ \Delta S^\circ = \sum S_{m}^\circ(\text{products}) - \sum S_{m}^\circ(\text{reactants}) \]where \(S_{m}^\circ\) is the standard molar entropy of each substance.
03

Insert the Given Standard Molar Entropies

Insert the given standard molar entropies into the formula: \[ \Delta S^\circ = [2 \times S_{m}^\circ(\mathrm{Fe}, s) + 3 \times S_{m}^\circ(\mathrm{H}_{2} \mathrm{O}, l)] - [S_{m}^\circ(\mathrm{Fe}_{2} \mathrm{O}_{3}, s) + 3 \times S_{m}^\circ(\mathrm{H}_{2}, g)] \]
04

Calculate the Standard Entropy Change

Perform the calculation: \[ \Delta S^\circ = [(2 \times 27.3) + (3 \times 69.9)] - [(87.4) + (3 \times 130.7)] \]\[ \Delta S^\circ = (54.6 + 209.7) - (87.4 + 392.1) \]\[ \Delta S^\circ = 264.3 - 479.5 \]\[ \Delta S^\circ = -215.2 \, \mathrm{JK}^{-1} \mathrm{mol}^{-1} \]

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Key Concepts

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

Thermodynamics
Thermodynamics is a branch of physical science that deals with the relations between heat and other forms of energy. In the context of chemistry, thermodynamics helps us understand how energy is transferred during chemical reactions and how it influences the properties of substances. One fundamental concept in thermodynamics is the principle of entropy, which is a measure of the disorder or randomness in a system. The second law of thermodynamics states that for any spontaneous process, the total entropy of the system and its surroundings always increases.

In practical terms, calculating the entropy change, such as the standard entropy change (\(\Delta S^\circ\)), for a reaction offers insights into the feasibility of the reaction and the amount of energy that might be dispersed into the surroundings. This is critical in predicting how reactions occur and designing processes that take these energy changes into account.
Chemical Reactions
Chemical reactions involve the transformation of one or more substances into different substances, and thermodynamics allows chemists to predict if and how a reaction will proceed. Entropy change is a significant aspect of chemical reactions because it gives an idea of the energy distribution. A reaction may be favorable if it increases the entropy of the surroundings, often releasing energy. Conversely, reactions that lead to a decrease in entropy are typically non-spontaneous unless energy is provided.

The computation of the entropy change is especially important for understanding endothermic and exothermic reactions. For instance, our exercise shows a negative entropy change (\(-215.2 \, \mathrm{JK}^{-1} \mathrm{mol}^{-1}\)) indicating that the reaction might not proceed spontaneously under standard conditions, as it leads to a decrease in the system's disorder.
Physical Chemistry
Physical chemistry is the study of how matter behaves on a molecular and atomic level and how chemical reactions occur. Within this field, thermodynamics plays an essential role, providing quantitative data about the changes that occur during reactions. Standard entropy change calculations, like the one we've discussed, help in determining the direction and spontaneity of chemical reactions.

Understanding these concepts is fundamental for students who wish to apply physical chemistry principles to real-world scenarios in industries such as pharmaceuticals, energy, and materials science. The ability to perform accurate calculations of entropy changes is a skill that ties together the theoretical and practical aspects of physical chemistry.
JEE Exam Preparation
Students preparing for competitive exams like the Joint Entrance Examination (JEE) in India need to have a strong understanding of thermodynamics, including entropy and Gibbs free energy. Proficiency in calculating entropy changes for chemical reactions is crucial, as it forms a key concept not only in physical chemistry but also in engineering applications.

For effective JEE exam preparation, students should practice a variety of entropy calculation problems. This will help them develop the necessary problem-solving skills and apply the thermodynamic principles confidently. Furthermore, understanding the theoretical underpinnings of these calculations, as explained in the previous sections, is vital for a deep and intuitive grasp of the subject matter required to excel in such competitive exams.

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Most popular questions from this chapter

10 mole of ideal gas expand isothermally and reversibly from a pressure of \(10 \mathrm{~atm}\) to \(1 \mathrm{~atm}\) at \(300 \mathrm{~K}\). What is the largest mass which can lifted through a height of 100 meter? (a) \(31842 \mathrm{~kg}\) (b) \(58.55 \mathrm{~kg}\) (c) \(342.58 \mathrm{~kg}\) (d) None of these

For a process to be spontaneous at constant \(T\) and \(P\) : (a) \((\Delta G)_{\text {system }}\) must be negative (b) \((\Delta G)_{\text {system }}\) must be positive (c) \((\Delta S)_{\text {system }}\) must be positive (d) \((\Delta S)_{\text {system }}\) must be negative

Which of the following is not correct? (a) Dissolution of \(\mathrm{NH}_{4} \mathrm{Cl}\) in excess of water is an endothermic process (b) Neutralisation is always exothermic (c) The absolute value of enthalpy (H) can be determined experimentally (d) The heat of reaction at constant volume is denoted by \(\Delta E\)

Calculate the standard enthalpy of reaction for the following reaction using the listed enthalpies of reaction : $$ \begin{aligned} 3 \mathrm{Co}(s)+2 \mathrm{O}_{2}(g) & \longrightarrow \mathrm{Co}_{3} \mathrm{O}_{4}(s) \\ 2 \mathrm{Co}(s)+\mathrm{O}_{2}(g) & \longrightarrow 2 \mathrm{CoO}(s) ; \quad \Delta H_{1}^{\circ}=-475.8 \mathrm{~kJ} \\ 6 \mathrm{CoO}(s)+\mathrm{O}_{2}(g) & \longrightarrow 2 \mathrm{Co}_{3} \mathrm{O}_{4}(s) ; \Delta H_{2}^{\circ}=-355.0 \mathrm{~kJ} \end{aligned} $$ (a) \(-891.2 \mathrm{~kJ}\) (b) \(-120.8 \mathrm{~kJ}\) (c) \(+891.2 \mathrm{~kJ}\) (d) \(-830.8 \mathrm{~kJ}\)

Which of the following exprésstons' is 'true for an ideal gas ? (a) \(\left(\frac{\partial V}{\partial T}\right)_{P}=0\) (b) \(\left(\frac{\partial P}{\partial T}\right)_{V: n}=0^{6}\) (c) \(\left(\frac{\partial U}{\partial V}\right)_{T}=0\) (d) \(\left(\frac{\partial U}{\partial T}\right)_{V}=0\)

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