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The \(\Delta \mathrm{H}_{\mathrm{f}}^{\circ}\) for \(\mathrm{CO}_{2}(\mathrm{~g}), \mathrm{CO}(\mathrm{g})\) and \(\mathrm{H}_{2} \mathrm{O}(\mathrm{g})\) are \(-393.5\), \(-110.5\) and \(-241.8 \mathrm{~kJ} \mathrm{~mol}^{-1}\) respectively. The standard enthalpy change (in \(\mathrm{kJ}\) ) for the reaction: \(\mathrm{CO}_{2}(\mathrm{~g})+\mathrm{H}_{2}(\mathrm{~g}) \longrightarrow \mathrm{CO}(\mathrm{g})+\mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \mathrm{is}\) (a) \(524.1\) (b) \(41.2\) (c) \(-262.5\) (d) \(-41.2\)

Short Answer

Expert verified
The standard enthalpy change is \(41.2 \, \mathrm{kJ}\).

Step by step solution

01

Write the Reaction Formula

The given reaction is \( \mathrm{CO}_{2}(\mathrm{~g}) + \mathrm{H}_{2}(\mathrm{~g}) \longrightarrow \mathrm{CO}(\mathrm{g}) + \mathrm{H}_{2}\mathrm{O}(\mathrm{g}) \). We need to calculate the standard enthalpy change for this reaction.
02

Recall the Formula for Enthalpy Change

The standard enthalpy change for a reaction \( \Delta H_{\text{reaction}}^{\circ} \) is calculated using the formula: \[ \Delta H_{\text{reaction}}^{\circ} = \sum \Delta H_{f}^{\circ}(\text{products}) - \sum \Delta H_{f}^{\circ}(\text{reactants}) \] where \( \Delta H_{f}^{\circ} \) is the standard enthalpy of formation.
03

Input Values for Products and Reactants

For the products, \( \Delta H_{f}^{\circ}(\mathrm{CO}(\mathrm{g})) = -110.5 \, \mathrm{kJ} \, \mathrm{mol}^{-1} \) and \( \Delta H_{f}^{\circ}(\mathrm{H}_{2}\mathrm{O}(\mathrm{g})) = -241.8 \, \mathrm{kJ} \, \mathrm{mol}^{-1} \). For the reactants, \( \Delta H_{f}^{\circ}(\mathrm{CO}_{2}(\mathrm{~g})) = -393.5 \, \mathrm{kJ} \, \mathrm{mol}^{-1} \) and \( \Delta H_{f}^{\circ}(\mathrm{H}_{2}(\mathrm{~g})) = 0 \, \mathrm{kJ} \, \mathrm{mol}^{-1} \) since it is an element in its standard state.
04

Calculate the Enthalpy Change for the Reaction

Substitute the values into the formula: \[ \Delta H_{\text{reaction}}^{\circ} = [(-110.5) + (-241.8)] - [(-393.5) + 0] \] This simplifies to: \[ \Delta H_{\text{reaction}}^{\circ} = (-352.3) - (-393.5) = 41.2 \, \mathrm{kJ} \]

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Key Concepts

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

Enthalpy Change
Enthalpy change, represented by \( \Delta H \), is a crucial concept in thermodynamics. It refers to the heat content variation between reactants and products during a chemical reaction under constant pressure conditions. Understanding enthalpy change helps to determine if a reaction is exothermic (releases heat) or endothermic (absorbs heat). In essence, \( \Delta H \) is calculated using the formula:
  • \( \Delta H_{\text{reaction}}^{\circ} = \sum \Delta H_{f}^{\circ}(\text{products}) - \sum \Delta H_{f}^{\circ}(\text{reactants}) \)
This method involves subtracting the total enthalpy of the reactants from the total enthalpy of the products. If the result is negative, the reaction releases heat, and if positive, it absorbs heat.
In our exercise, we found \( \Delta H_{\text{reaction}}^{\circ} = 41.2 \, \mathrm{kJ} \), indicating the process absorbs heat.
Enthalpy of Formation
The enthalpy of formation, denoted by \( \Delta H_{f}^{\circ} \), is a specific type of enthalpy change. It refers to the change in enthalpy when one mole of a compound is formed from its elements in their standard states. This value helps assess the energy efficiency of producing compounds. Values for the enthalpies of formation are usually given in \( \mathrm{kJ} \, \mathrm{mol}^{-1} \).
  • For our chemical reaction calculation:
    • \( \Delta H_{f}^{\circ}(\mathrm{CO}_{2}(\mathrm{g})) = -393.5 \, \mathrm{kJ} \, \mathrm{mol}^{-1} \)
    • \( \Delta H_{f}^{\circ}(\mathrm{CO}(\mathrm{g})) = -110.5 \, \mathrm{kJ} \, \mathrm{mol}^{-1} \)
    • \( \Delta H_{f}^{\circ}(\mathrm{H}_{2} \mathrm{O}(\mathrm{g})) = -241.8 \, \mathrm{kJ} \, \mathrm{mol}^{-1} \)
    • \( \Delta H_{f}^{\circ}(\mathrm{H}_{2}(\mathrm{g})) = 0 \, \mathrm{kJ} \, \mathrm{mol}^{-1} \)
These described values are critical for calculating the standard enthalpy change of reactions, as they provide the necessary basis for determining the energy absorbed or released.
Chemical Reaction
Chemical reactions are the basis of chemistry, involving the transformation of reactants into products. This transformation is often coupled with an energy exchange, which can be measured and analyzed through thermodynamic principles.
The specific reaction in our example is:
  • \( \mathrm{CO}_{2}(\mathrm{g}) + \mathrm{H}_{2}(\mathrm{g}) \longrightarrow \mathrm{CO}(\mathrm{g}) + \mathrm{H}_{2} \mathrm{O}(\mathrm{g}) \)
This reaction highlights the conversion of carbon dioxide and hydrogen gas into carbon monoxide and water vapor. Expressing this process helps us understand which bonds are broken and formed, providing insights into the enthalpy changes involved.
Understanding the dynamics of chemical reactions, alongside enthalpy changes, allows scientists and students to predict how energy-efficient and feasible reactions are.

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Most popular questions from this chapter

In the conversion of lime stone to lime, \(\mathrm{CaCO}_{3}(\mathrm{~s}) \longrightarrow \mathrm{CaO}(\mathrm{s})+\mathrm{CO}_{2}(\mathrm{~g})\) The values of \(\Delta \mathrm{H}^{\circ}\) and \(\Delta \mathrm{S}^{\circ}\) are \(+179.1 \mathrm{~kJ} \mathrm{~mol}^{-1}\) and \(160.2 \mathrm{~J} / \mathrm{K}\) respectively at \(298 \mathrm{~K}\) and 1 bar. Assuming that \(\Delta \mathrm{H}^{\circ}\) and \(\Delta \mathrm{S}^{\circ}\) do not change with temperature, temperature above which conversion of limestone to lime will be spontaneous is: (a) \(1200 \mathrm{~K}\) (b) \(845 \mathrm{~K}\) (c) \(1118 \mathrm{~K}\) (d) \(1008 \mathrm{~K}\)

The increase in internal energy of the system is \(100 \mathrm{~J}\) when \(300 \mathrm{~J}\) of heat is supplied to it. What is the amount of work done by the system? (a) - 200 J (b) \(+200 \mathrm{~J}\) (c) \(-300 \mathrm{~J}\) (d) - 400 J

Which of the following reaction defines \(\Delta \mathrm{H}_{\mathrm{f}}^{\mathrm{o}}\) ? (a) \(\mathrm{C}\) (diamond) \(+\mathrm{O}_{2}(\mathrm{~g}) \longrightarrow \mathrm{CO}_{2}(\mathrm{~g})\) (b) \(\frac{1}{2} \mathrm{H}_{2}(\mathrm{~g})+\frac{1}{2} \mathrm{~F}_{2}(\mathrm{~g}) \longrightarrow \mathrm{HF}(\mathrm{g})\) (c) \(\mathrm{N}_{2}(\mathrm{~g})+3 \mathrm{H}_{2}(\mathrm{~g}) \longrightarrow 2 \mathrm{NH}_{3}(\mathrm{~g})\) (d) \(\mathrm{CO}(\mathrm{g})+\frac{1}{2} \mathrm{O}_{2}(\mathrm{~g}) \longrightarrow \mathrm{CO}_{2}(\mathrm{~g})\)

Internal energy of a substance/system is a: (a) State function (b) Path function (c) Work function (d) None

The standard entropy change for the reaction: \(\mathrm{SO}_{2}(\mathrm{~g})+\frac{1}{2} \mathrm{O}_{2}(\mathrm{~g}) \longrightarrow \mathrm{SO}_{3}(\mathrm{~g})\) is (where \(\mathrm{S}^{\circ}\) for \(\mathrm{SO}_{2}\) (g), \(\mathrm{O}_{2}(\mathrm{~g})\) and \(\mathrm{SO}_{3}(\mathrm{~g})\) are \(248.5,205\) and \(256.2\) J \(\mathrm{K}^{-1} \mathrm{~mol}^{-1}\) respectively) (a) \(198.2 \mathrm{~J} \mathrm{~K}^{-1} \mathrm{~mol}^{-1} \quad\) (b) \(-192.8 \mathrm{~J} \mathrm{~K}^{-1} \mathrm{~mol}^{-1}\) (c) \(-94.8 \mathrm{~J} \mathrm{~K}^{-1} \mathrm{~mol}^{-1}\) (d) \(94.8 \mathrm{~J} \mathrm{~K}^{-1} \mathrm{~mol}^{-1}\)

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