Problem 69
Question
Consider the following reaction between oxides of nitrogen: $$ \mathrm{NO}_{2}(g)+\mathrm{N}_{2} \mathrm{O}(g) \longrightarrow 3 \mathrm{NO}(g) $$ (a) Use data in Appendix \(C\) to predict how \(\Delta G\) for the reaction varies with increasing temperature. (b) Calculate \(\Delta G\) at \(800 \mathrm{~K}\), assuming that \(\Delta H^{\circ}\) and \(\Delta S^{\circ}\) do not change with temperature. Under standard conditions is the reaction spontaneous at \(800 \mathrm{~K} ?\) (c) Calculate \(\Delta G\) at \(1000 \mathrm{~K}\). Is the reaction spontaneous under standard conditions at this temperature?
Step-by-Step Solution
Verified Answer
(a) The Gibbs Free Energy equation is given by \(\Delta G = \Delta H - T \Delta S\). (b) At 800 K, we have \(\Delta H = 55.8 \: kJ\), \(\Delta S = 173.5 \: J/K\), and \(\Delta G = -84,000 \: J/mol\). The reaction is spontaneous at 800 K, as \(\Delta G\) is negative. (c) At 1000 K, \(\Delta G = -117,700 \: J/mol\), which means the reaction is also spontaneous under standard conditions at 1000 K.
1Step 1: a) Knowing the Gibbs Free Energy Equation:
We need to know the Gibbs Free Energy equation which is as follows:
\[
\Delta G = \Delta H - T \Delta S
\]
where ∆G is the change in Gibbs free energy, ∆H is the change in enthalpy, T is the temperature in Kelvin, and ∆S is the change in entropy.
2Step 2: b) Calculating ∆G at 800 K:
We are given that ∆H° and ∆S° do not change with temperature. Using the data given in Appendix C, we have:
∆H°(NO2) = 33.1 kJ/mol, ∆S°(NO2) = 240.0 J/mol·K
∆H°(N2O) = 82.0 kJ/mol, ∆S°(N2O) = 218.6 J/mol·K
∆H°(NO) = 90.3 kJ/mol, ∆S°(NO) = 210.7 J/mol·K
Now, we have to calculate the ∆H and ∆S of the reaction by using stoichiometric coefficients.
∆H = [3∆H°(NO)] - [∆H°(NO2) + ∆H°(N2O)] = (3*90.3) - (33.1+82.0) = 55.8 kJ
∆S = [3∆S°(NO)] - [∆S°(NO2) + ∆S°(N2O)] = (3*210.7) - (240.0+218.6) = 173.5 J/K
Now we can calculate ∆G at 800 K:
∆G = ∆H - T∆S = 55.8*10^3 J/mol - (800 K)(173.5 J/mol·K) = -84,000 J/mol
As ∆G is negative, the reaction is spontaneous at 800 K.
3Step 3: c) Calculating ∆G at 1000 K:
We already have ∆H and ∆S for the reaction; we only need to change the temperature in the equation for Gibbs Free Energy.
∆G = ∆H - T∆S = 55.8*10^3 J/mol - (1000 K)(173.5 J/mol·K) = -117,700 J/mol
As ∆G is negative at 1000 K, the reaction is spontaneous under standard conditions at this temperature as well.
Key Concepts
Spontaneous ReactionEnthalpy ChangeEntropy Change
Spontaneous Reaction
A reaction is considered spontaneous if it occurs on its own without any external input of energy once it has begun. The spontaneity of a reaction is often determined by the change in Gibbs Free Energy (\(\Delta G\)). When \(\Delta G\) is negative, the reaction proceeds spontaneously. This negativity indicates that the reaction releases energy, typically resulting in a more stable, lower energy state of the system.
- Negative \(\Delta G\): Spontaneous reaction (energy is released)
- Positive \(\Delta G\): Non-spontaneous reaction (energy is required)
- Zero \(\Delta G\): Reaction at equilibrium (no net change occurs)
Enthalpy Change
Enthalpy change (\(\Delta H\)) is the amount of heat released or absorbed during a chemical reaction at constant pressure. It's a crucial factor in the determination of reaction spontaneity and can be either positive or negative.
- Exothermic reaction (\(\Delta H < 0\)): Releases heat, contributing to a potentially negative \(\Delta G\).
- Endothermic reaction (\(\Delta H > 0\)): Absorbs heat, which may require careful consideration regarding \(\Delta G\).
Entropy Change
Entropy change (\(\Delta S\)) reflects the degree of disorder or randomness in a system. A positive \(\Delta S\) indicates an increase in entropy or disorder, often favoring spontaneity in a reaction.
- Positive \(\Delta S\): Greater disorder, often leads to a negative \(\Delta G\).
- Negative \(\Delta S\): Lesser disorder, could increase \(\Delta G\).
Other exercises in this chapter
Problem 64
From the values given for \(\Delta H^{\circ}\) and \(\Delta S^{\circ},\) calculate \(\Delta G^{\circ}\) for each of the following reactions at \(298 \mathrm{~K}
View solution Problem 67
For a particular reaction, \(\Delta H=30.0 \mathrm{~kJ}\) and \(\Delta S=90.0 \mathrm{~J} / \mathrm{K}\). Assume that \(\Delta H\) and \(\Delta S\) do not vary
View solution Problem 72
(a) Using data in Appendix \(C\), estimate the temperature at which the free- energy change for the transformation from \(\mathrm{I}_{2}(s)\) to \(\mathrm{I}_{2
View solution Problem 73
Acetylene gas, \(\mathrm{C}_{2} \mathrm{H}_{2}(g)\), is used in welding. (a) Write a balanced equation for the combustion of acetylene gas to \(\mathrm{CO}_{2}(
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