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\( \left. \begin{array} { l } { ( S _ { 2 } ( l ) + 3 O _ { 2 } ( g ) \div CO _ { 2 } ( g ) + { } _ { 2 } SO _ { 2 } ( g ) \Delta H = ? } \\ { C _ { ( s ) } + C _ { 2 } ( g ) \rightarrow CO _ { 2 } ( g ) \Delta H = - 39,3.5 kJ } \\ { S ( s ) + O _ { 2 } ( g ) \geq SO _ { 2 } ( g ) \quad \Delta H = - 296.8 kJ } \\ { C ( s ) + 2 S _ { s } ( s ) \rightarrow CS _ { 2 } ( l ) \quad CH = + 87.9 kJJ } \end{array} \right. \)

Ask by Turnbull Collins. in the Philippines
Feb 25,2025

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The enthalpy change for the reaction \( S_2(l) + 3O_2(g) \rightarrow SO_2(g) \) is \( \Delta H = -720.8 \, \text{kJ} \).

Solución

To solve the problem, we need to determine the enthalpy change (\( \Delta H \)) for the reaction involving \( S_2(l) \), \( O_2(g) \), and \( SO_2(g) \). We will use Hess's law, which states that the total enthalpy change for a reaction is the sum of the enthalpy changes for the individual steps of the reaction. ### Known Reactions and Their Enthalpy Changes 1. \( C(s) + C_2(g) \rightarrow CO_2(g) \quad \Delta H = -39.3 \, \text{kJ} \) 2. \( S(s) + O_2(g) \rightarrow SO_2(g) \quad \Delta H = -296.8 \, \text{kJ} \) 3. \( C(s) + 2S(s) \rightarrow CS_2(l) \quad \Delta H = +87.9 \, \text{kJ} \) ### Target Reaction We need to find \( \Delta H \) for the reaction: \[ S_2(l) + 3O_2(g) \rightarrow SO_2(g) \] ### Steps to Solve 1. **Reverse the third reaction** to express \( S_2(l) \) in terms of \( S(s) \): \[ CS_2(l) \rightarrow C(s) + 2S(s) \quad \Delta H = -87.9 \, \text{kJ} \] 2. **Use the second reaction** as is to produce \( SO_2(g) \): \[ S(s) + O_2(g) \rightarrow SO_2(g) \quad \Delta H = -296.8 \, \text{kJ} \] 3. **Use the first reaction** to produce \( CO_2(g) \): \[ C(s) + C_2(g) \rightarrow CO_2(g) \quad \Delta H = -39.3 \, \text{kJ} \] ### Combining the Reactions Now we will combine these reactions to find the overall enthalpy change. 1. From the reversed third reaction: \[ CS_2(l) \rightarrow C(s) + 2S(s) \quad \Delta H = -87.9 \, \text{kJ} \] 2. From the second reaction: \[ S(s) + O_2(g) \rightarrow SO_2(g) \quad \Delta H = -296.8 \, \text{kJ} \] 3. We need to adjust the second reaction to account for the stoichiometry of \( S_2(l) \) and \( O_2(g) \). Since we need 2 moles of \( S(s) \) to form \( S_2(l) \), we will multiply the second reaction by 2: \[ 2S(s) + 2O_2(g) \rightarrow 2SO_2(g) \quad \Delta H = 2 \times (-296.8) = -593.6 \, \text{kJ} \] ### Final Calculation Now we can sum the enthalpy changes: \[ \Delta H = (-87.9) + (-593.6) + (-39.3) \] Calculating this gives: \[ \Delta H = -87.9 - 593.6 - 39.3 = -720.8 \, \text{kJ} \] ### Conclusion The enthalpy change for the reaction \( S_2(l) + 3O_2(g) \rightarrow SO_2(g) \) is: \[ \Delta H = -720.8 \, \text{kJ} \]

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Did you know that thermochemistry is more than just a collection of equations? It plays a crucial role in understanding how reactions release or absorb heat, which is essential in various fields, from industry to environmental science. The values of ΔH, or enthalpy change, guide chemists in predicting the energy changes in reactions, ultimately aiding in developing efficient energy sources and materials! When tackling thermodynamic problems, common mistakes often occur during unit conversions or sign errors on ΔH values. Always double-check your process: ensure you're using the correct phase for substances and are mindful of whether your reaction is exothermic (negative ΔH) or endothermic (positive ΔH). Clear tracking of these details can prevent headaches down the line!

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