Math Problem Statement

Calculate the temperature at which each of the following reactions becomes spontaneous.

(a)    CaO(s) + H2O(l)  Ca(OH)2(s)

Solution

To determine the temperature at which a reaction becomes spontaneous, we use the Gibbs free energy equation:

ΔG=ΔHTΔS\Delta G = \Delta H - T \Delta S

A reaction becomes spontaneous when ΔG<0\Delta G < 0. Therefore, for spontaneity:

ΔHTΔS<0orT>ΔHΔS\Delta H - T \Delta S < 0 \quad \text{or} \quad T > \frac{\Delta H}{\Delta S}

Where:

  • ΔH\Delta H is the enthalpy change of the reaction.
  • ΔS\Delta S is the entropy change of the reaction.
  • TT is the temperature at which the reaction becomes spontaneous (in Kelvin).

Now, for the reaction:

CaO(s)+H2O(l)Ca(OH)2(s)\text{CaO(s)} + \text{H}_2\text{O(l)} \rightarrow \text{Ca(OH)}_2\text{(s)}

We need the values of ΔH\Delta H and ΔS\Delta S, which are typically found in thermodynamic tables.

Step 1: Gathering Thermodynamic Data

  • Standard enthalpy of formation (ΔHf\Delta H_f^\circ) and entropy (SS^\circ) for each substance at standard conditions (298 K):
    • CaO(s):
      • ΔHf=635.1kJ/mol\Delta H_f^\circ = -635.1 \, \text{kJ/mol}
      • S=39.8J/(mol\cdotpK)S^\circ = 39.8 \, \text{J/(mol·K)}
    • H2O(l):
      • ΔHf=285.8kJ/mol\Delta H_f^\circ = -285.8 \, \text{kJ/mol}
      • S=69.9J/(mol\cdotpK)S^\circ = 69.9 \, \text{J/(mol·K)}
    • Ca(OH)2(s):
      • ΔHf=986.1kJ/mol\Delta H_f^\circ = -986.1 \, \text{kJ/mol}
      • S=83.4J/(mol\cdotpK)S^\circ = 83.4 \, \text{J/(mol·K)}

Step 2: Calculate ΔH\Delta H and ΔS\Delta S

ΔH=ΔHf(products)ΔHf(reactants)\Delta H = \sum \Delta H_f^\circ \, \text{(products)} - \sum \Delta H_f^\circ \, \text{(reactants)}

ΔS=S(products)S(reactants)\Delta S = \sum S^\circ \, \text{(products)} - \sum S^\circ \, \text{(reactants)}

Enthalpy change (ΔH\Delta H):

[ \Delta H = [-986.1 , \text{kJ/mol}] - [-635.1 , \text{kJ/mol} + (-285.8 , \text{kJ/mol})] ]

ΔH=986.1(920.9)=65.2kJ/mol\Delta H = -986.1 - (-920.9) = -65.2 \, \text{kJ/mol}

Entropy change (ΔS\Delta S):

[ \Delta S = [83.4 , \text{J/(mol·K)}] - [39.8 , \text{J/(mol·K)} + 69.9 , \text{J/(mol·K)}] ]

ΔS=83.4109.7=26.3J/(mol\cdotpK)\Delta S = 83.4 - 109.7 = -26.3 \, \text{J/(mol·K)}

Step 3: Calculate the temperature at which the reaction becomes spontaneous

To find the temperature where the reaction becomes spontaneous, we set ΔG=0\Delta G = 0:

T=ΔHΔST = \frac{\Delta H}{\Delta S}

Convert ΔH\Delta H to J/mol:

ΔH=65.2kJ/mol=65200J/mol\Delta H = -65.2 \, \text{kJ/mol} = -65200 \, \text{J/mol}

Now, calculate the temperature:

T=6520026.3KT = \frac{-65200}{-26.3} \, \text{K}

T=2479KT = 2479 \, \text{K}

Conclusion:

The reaction becomes spontaneous at a temperature above 2479 K.


Would you like further details on this or have any other questions?

Here are 5 related questions to explore:

  1. What is the significance of ΔG=0\Delta G = 0 in thermodynamics?
  2. How do enthalpy and entropy influence the spontaneity of a reaction?
  3. What are the typical temperature ranges for various industrial reactions?
  4. How is Gibbs free energy used in biological systems?
  5. What methods can be used to experimentally determine ΔH\Delta H and ΔS\Delta S?

Tip: Always ensure that your thermodynamic data is consistent, using the same units when performing calculations.

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Math Problem Analysis

Mathematical Concepts

Thermodynamics
Gibbs Free Energy
Enthalpy
Entropy

Formulas

ΔG = ΔH - TΔS
T = ΔH / ΔS

Theorems

Gibbs Free Energy Theorem
Spontaneity Condition (ΔG < 0)

Suitable Grade Level

College/University Level (Thermodynamics, Chemistry)