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Calculate the Delta(r)G^(@) for the reac...

Calculate the `Delta_(r)G^(@)` for the reaction:
`C_(6)H_(12)O_(6)(s) + 6O_(2)(g) to 6CO_(2)(g) + 6H_(2)O(l)`
`Delta_(f)G^(@)` values (kJ `mol^(-1)`) are :
`C_(12)H_(12)O_(6)(s) = -910.2, CO_(2)(g) = -394.4, H_(2)O(l) = -237.2`

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To calculate the standard Gibbs free energy change (Δ_rG°) for the reaction: \[ \text{C}_6\text{H}_{12}\text{O}_6(s) + 6\text{O}_2(g) \rightarrow 6\text{CO}_2(g) + 6\text{H}_2\text{O}(l) \] we will use the standard Gibbs free energy of formation (Δ_fG°) values provided: - Δ_fG° for C₆H₁₂O₆(s) = -910.2 kJ/mol - Δ_fG° for CO₂(g) = -394.4 kJ/mol - Δ_fG° for H₂O(l) = -237.2 kJ/mol - Δ_fG° for O₂(g) = 0 kJ/mol (since it is in its standard state) ### Step-by-Step Solution: 1. **Write the Gibbs Free Energy Change Equation:** The standard Gibbs free energy change for the reaction can be calculated using the formula: \[ \Delta_rG° = \sum (\Delta_fG° \text{ of products}) - \sum (\Delta_fG° \text{ of reactants}) \] 2. **Calculate the Gibbs Free Energy of Products:** For the products, we have: - 6 moles of CO₂: \[ 6 \times (-394.4 \text{ kJ/mol}) = -2366.4 \text{ kJ} \] - 6 moles of H₂O: \[ 6 \times (-237.2 \text{ kJ/mol}) = -1423.2 \text{ kJ} \] - Total Gibbs Free Energy for products: \[ -2366.4 \text{ kJ} + (-1423.2 \text{ kJ}) = -3789.6 \text{ kJ} \] 3. **Calculate the Gibbs Free Energy of Reactants:** For the reactants, we have: - 1 mole of C₆H₁₂O₆: \[ -910.2 \text{ kJ} \] - 6 moles of O₂ (which is 0): \[ 6 \times 0 \text{ kJ} = 0 \text{ kJ} \] - Total Gibbs Free Energy for reactants: \[ -910.2 \text{ kJ} + 0 \text{ kJ} = -910.2 \text{ kJ} \] 4. **Substitute into the Gibbs Free Energy Change Equation:** Now substitute the values into the equation: \[ \Delta_rG° = (-3789.6 \text{ kJ}) - (-910.2 \text{ kJ}) \] \[ \Delta_rG° = -3789.6 + 910.2 = -2879.4 \text{ kJ} \] 5. **Final Result:** The standard Gibbs free energy change for the reaction is: \[ \Delta_rG° = -2879.4 \text{ kJ/mol} \]

To calculate the standard Gibbs free energy change (Δ_rG°) for the reaction: \[ \text{C}_6\text{H}_{12}\text{O}_6(s) + 6\text{O}_2(g) \rightarrow 6\text{CO}_2(g) + 6\text{H}_2\text{O}(l) \] we will use the standard Gibbs free energy of formation (Δ_fG°) values provided: - Δ_fG° for C₆H₁₂O₆(s) = -910.2 kJ/mol - Δ_fG° for CO₂(g) = -394.4 kJ/mol ...
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Consider the reaction, C_(6)H_(12)O_(6)(g)+6O_(2)(g) to 6CO_(2)(g) +6H_(2)O(l) , which of the following expressions is /are correct?

Calculate the standard Gibbs enegry change for the combustion of alpha-D glucose at 300K . C_(6)H_(12)O_(6)(s) +6O_(2)(g) rarr 6CO_(2)(g) +6H_(2)O(l) Given the standard enthalpies of formation (kJ mol^(-1)) C_(6)H_(12)O_(6) =- 1274.5, CO_(2) =- 393.5, H_(2)O =- 285.8 . Entropies (J K mol^(-1)) C_(6)H_(12)O_(6) = 212.1, O_(1) = 205.0, CO_(2) =213, H_(2)O = 69.9

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The value of x in balanced equation is C_(6)H_(12)O_(6(aq))+6O_(2(g))to"x"CO_(2(g))+6H_(2)O_((l))+"energy"

For the reaction , 2C_(2)H_(6)(g)+7O_(2)(g)rarr4CO_(2)(g)+6H_(2)O(l) , the rate of disappearnce of C_(2)H_(6)(g) :

Compounds with carbon-carbon double bond, such as ethylene, C_(2)H_(4) , add hydrogen in a reaction called hydrogenation. C_(2)H_(4)(g)+H_(2)(g) rarr C_(2)H_(6)(g) Calculate enthalpy change for the reaction, using the following combustion data C_(2)H_(4)(g) + 3O_(2)(g) rarr 2CO_(2)(g) + 2H_(2)O(g) , Delta_("comb")H^(Θ) = -1401 kJ mol^(-1) C_(2)H_(6)(g) + 7//2O_(2)(g)rarr 2CO_(2) (g) + 3H_(2)O(l) , Delta_("comb")H^(Θ) = -1550kJ H_(2)(g) + 1//2O_(2)(g) rarr H_(2)O(l) , Delta_("comb")H^(Θ) = -286.0 kJ mol^(-1)

Calculate Delta_(f)H^(@) for the reaction, CO_(2)(g) + H_(2)(g) to CO(g) + H_(2)O(g) Given that Delta_(f)H^(@) for CO_(2)(g) , CO(g) and H_(2)O(g) are -393.5, -111.3 and -241.8 kJ mol^(-1) respectively.

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