Determine the enthalpy of formation of \(\mathrm{B}_{2} \mathrm{H}_{6}(g)\) in \(\mathrm{kJ} / \mathrm{mol}\) of the following reaction. $$ \mathrm{B}_{2} \mathrm{H}_{6}(g)+3 \mathrm{O}_{2}(g) \longrightarrow \mathrm{B}_{2} \mathrm{O}_{3}(s)+3 \mathrm{H}_{2} \mathrm{O}(g) $$ Given : \(\Delta_{r} H^{\circ}=-1941 \cdot \mathrm{kJ} / \mathrm{mol} ; \quad \Delta H_{f}^{\circ}\left(\mathrm{B}_{2} \mathrm{O}_{3}, s\right)=-1273 \mathrm{~kJ} / \mathrm{mol}\) \(\mathrm{W}_{f}^{\circ}\left(\mathrm{H}_{2} \mathrm{O}, g\right)=-241.8 \mathrm{~kJ} / \mathrm{mol}\) (a) \(-75.6\) (b) \(+7 \overline{5} .6\) (c) \(-57.4\) (d) \(-28.4\)

Short Answer

Expert verified
-57.4 kJ/mol

Step by step solution

01

Write down known enthalpies

We have the enthalpy of reaction, \(\Delta_r H^\circ = -1941\ kJ/mol\), the enthalpy of formation for \(\mathrm{B}_2 \mathrm{O}_3(s)\), \(\Delta H_f^\circ(\mathrm{B}_2 \mathrm{O}_3, s) = -1273\ kJ/mol\), and the enthalpy of formation for \(\mathrm{H}_2 \mathrm{O}(g)\), \(\Delta H_f^\circ(\mathrm{H}_2 \mathrm{O}, g) = -241.8\ kJ/mol\).
02

Set up the enthalpy change of formation equation

The enthalpy change of the reaction can be represented as the sum of the enthalpy changes of formation of the products minus the sum of the enthalpy changes of formation of the reactants. We need to find the unknown \(\Delta H_f^\circ(\mathrm{B}_2 \mathrm{H}_6, g)\).
03

Calculate enthalpy change for products

The total enthalpy change for the products is the sum of the enthalpy of formation of \(\mathrm{B}_2 \mathrm{O}_3\) and \(3\) times the enthalpy of formation of \(\mathrm{H}_2 \mathrm{O}\) because there are \(3\) moles of \(\mathrm{H}_2 \mathrm{O}(g)\): \[ '\Delta H_p= \Delta H_f^\circ(\mathrm{B}_2 \mathrm{O}_3, s) + 3 \times \Delta H_f^\circ(\mathrm{H}_2 \mathrm{O}, g) = -1273\ kJ/mol + 3 \times (-241.8\ kJ/mol) \]
04

Express \(\Delta_r H^\circ\) using \(\Delta H_p\)

According to Hess's Law, \(\Delta_r H^\circ = \Delta H_p - \Delta H_f^\circ(\mathrm{B}_2 \mathrm{H}_6, g)\). Rearrange to solve for \(\Delta H_f^\circ(\mathrm{B}_2 \mathrm{H}_6, g)\): \[\Delta H_f^\circ(\mathrm{B}_2 \mathrm{H}_6, g) = \Delta H_p - \Delta_r H^\circ \]
05

Substitute the values into the equation

Substitute the given values into the equation to find the enthalpy of formation for \(\mathrm{B}_2 \mathrm{H}_6(g)\): \[\Delta H_f^\circ(\mathrm{B}_2 \mathrm{H}_6, g) = (-1273 + 3 \times (-241.8))\ kJ/mol - (-1941\ kJ/mol) = -1998.4\ kJ/mol + 1941\ kJ/mol \]
06

Solve for the enthalpy of formation

Now solve for \(\Delta H_f^\circ(\mathrm{B}_2 \mathrm{H}_6, g)\): \[\Delta H_f^\circ(\mathrm{B}_2 \mathrm{H}_6, g) = -57.4\ kJ/mol \]

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Key Concepts

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

Hess's Law
Understanding Hess's Law is fundamental when tackling enthalpy of formation problems in chemical thermodynamics. It states that the total enthalpy change during a chemical reaction is the same, regardless of the number of stages in which the reaction occurs. This is a powerful concept because it allows us to use known enthalpy values for individual reactions to calculate unknown ones, like in the given exercise.

In the context of our exercise, we apply Hess's Law by breaking down the reaction into a series of hypothetical steps whose enthalpies are known, facilitating the calculation of the enthalpy of formation for a compound. For instance, the enthalpy of formation for \(\mathrm{B}_2 \mathrm{H}_6(g)\) can be deduced if we have the enthalpy for the overall reaction and the enthalpies of formation for all other products and reactants.
Enthalpy Change Calculation
The calculation of enthalpy change allows chemists to predict the heat exchange associated with a chemical reaction. When determining the enthalpy of formation for \(\mathrm{B}_2 \mathrm{H}_6(g)\), we must consider both the reactants and products within the chemical reaction provided.

By writing the enthalpy change of the reaction as the difference between the sum of the enthalpies of formation of products and reactants, we can establish a formula that incorporates Hess's Law. In this exercise, we organized our known data and applied arithmetic to deduce the missing enthalpy value. It's imperative to account for the stoichiometry of the reaction, as the quantity of reactants and products can significantly affect the final enthalpy change calculation.
Chemical Thermodynamics
Chemical thermodynamics is the study of the energy and heat associated with chemical reactions and physical changes. One of its core components is enthalpy, a measure of the heat content in a system at constant pressure.

The enthalpy of formation is a specific type of enthalpy change and refers to the heat change that occurs when one mole of a substance is formed from its elements at their standard states. Through problems such as the one presented, students engage with chemical thermodynamics by learning to compute these changes. This is vital for predicting reaction spontaneity and feasibilities in real-world scenarios, ranging from industrial processes to environmental change predictions.
IIT JEE Chemistry
The Indian Institutes of Technology Joint Entrance Examination (IIT JEE) is a highly competitive exam among aspiring engineering undergraduates. Chemistry is one of the critical subjects in this exam, covering topics like chemical thermodynamics and enthalpy calculations.

For IIT JEE aspirants, mastering problems involving Hess's Law and enthalpy of formation is essential. The exam requires a deep understanding of concepts, accuracy, and speed in problem-solving. Therefore, solving exercises similar to the provided one is an excellent practice, as it trains students to quickly grasp the concepts and apply their knowledge efficiently under exam conditions.

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Most popular questions from this chapter

With what minimum pressure (in \(k P a\) ), a given volume of an ideal gas \(\left(C_{p, m}=7 / 2 R\right.\) ), originally at \(400 \mathrm{~K}\) and \(100 \mathrm{kPa}\) pressure can be compressed irreversibly adiabatically in order to raise its temperature to \(600 \mathrm{~K}\) : (a) \(362.5 \mathrm{kPa}\) (b) \(275 \mathrm{kPa}\) (c) \(437.5 \mathrm{kPa}\) (d) \(550 \mathrm{kPa}\)

Stearic acid \(\left[\mathrm{CH}_{3}\left(\mathrm{CH}_{2}\right)_{16} \mathrm{CO}_{2} \mathrm{H}\right]\) is a fatty acid, the part of fat that stores most of the energy. \(1.0 \mathrm{~g}\) of stearic acid was burned in a bomb calorimeter. The bomb had a heat capacity of 652 \(\mathrm{~J} /{ }^{\circ} \mathrm{C} .\) If the temperature of \(500 \mathrm{~g}\) water \(\left(c=4.18 \mathrm{~J} / \mathrm{g}^{\circ} \mathrm{C}\right)\) rose from \(25.0\) to \(39.3^{\circ} \mathrm{C}\), how much heat was released when the stearic acid was burned? \(\left[\right.\) Given \(\left.C_{p}\left(\mathrm{H}_{2} \mathrm{O}\right)=4.18 \mathrm{~J} / \mathrm{g}^{\circ} \mathrm{C}\right]\) (a) \(39.21 \mathrm{~kJ}\) (b) \(29.91 \mathrm{~kJ}\) (c) \(108 \mathrm{~kJ}\) \(\begin{array}{llll}\text { (d) } 9.32 \mathrm{~kJ} & \therefore \therefore\end{array}\)

The entropy change for a phase transformation is : (a) \(\frac{\Delta U}{\gamma+d T}\) (b) \(\frac{\Delta T}{\Delta H}\) (c) \(\frac{\Delta H}{T}\) (d) \(\frac{\Delta H+\Delta G}{T}\)

One mole of an ideal gas \(\left(C_{v, m}=\frac{5}{2} R\right)\) at \(300 \mathrm{~K}\) and \(5 \mathrm{~atm}\) is expanded adiabatically to a final pressure of 2 atm against a constant pressure of 2 atm. Final temperature of the gas is : (a) \(270 \mathrm{~K}\) (b) \(273 \mathrm{~K}\) (c) \(248.5 \mathrm{~K}\) (d) \(200 \mathrm{~K}\)

Temperature of 1 mole of a gas is increased by \(2^{\circ} \mathrm{C}\) at constant pressure, work done is : (a) \(R\) (b) \(2 R\) (c) \(R / 2\) (d) \(3 R\)

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