For the reaction CO(g) + \(\frac{1}{2}\) O\(_2\)(g) \(\rightarrow\) CO\(_2\)(g) Which one of the statement is correct at constant T and P?
Show Hint
Just count the moles of gases!
If products have fewer moles of gas (\(\Delta n_g \textless 0\)), then \(\Delta H \textless \Delta E\).
If products have more moles of gas (\(\Delta n_g \textgreater 0\)), then \(\Delta H \textgreater \Delta E\).
\(\Delta H\) is independent of physical state of the reactants
Show Solution
The Correct Option isB
Solution and Explanation
Step 1: Understanding the Concept:
The relationship between enthalpy change ($\Delta H$) and internal energy change ($\Delta E$, also denoted as $\Delta U$) for a gaseous reaction is governed by the change in the number of moles of gaseous products and reactants. Step 2: Key Formula or Approach:
\[ \Delta H = \Delta E + \Delta n_g RT \]
where $\Delta n_g = (\text{Total moles of gaseous products}) - (\text{Total moles of gaseous reactants})$. Step 3: Detailed Explanation:
1. Write the balanced equation: $CO(g) + \frac{1}{2}O_{2}(g) \rightarrow CO_{2}(g)$.
2. Calculate $\Delta n_g$:
- Moles of products = 1 ($CO_2$).
- Moles of reactants = $1 + 0.5 = 1.5$ ($CO$ and $O_2$).
- $\Delta n_g = 1 - 1.5 = -0.5$.
3. Substitute $\Delta n_g$ into the formula:
\[ \Delta H = \Delta E + (-0.5)RT \]
\[ \Delta H = \Delta E - 0.5RT \]
4. Since $R$ and $T$ are positive, we are subtracting a positive value from $\Delta E$ to get $\Delta H$. This means $\Delta H$ is smaller than $\Delta E$. Step 4: Final Answer
At constant $T$ and $P$, $\Delta H<\Delta E$.