Use the ΔH°f and ΔH°rxn information provided to calculate ΔH°f
for SO3(g):
2 SO2(g) + O2(g) → 2 SO3(g) ΔH°rxn = -198 kJ
ΔH°f (kJ/mol)
SO2(g) -297
Use the ΔH°f and ΔH°rxn information provided to calculate ΔH°f for SO3(g): 2 SO2(g) + O2(g)...
Use the AHⓇ and AH°rxn information provided to calculate AHºf for SO3(g): AHºf (kJ/mol) | 2 SO2(g) + O2(g) → 2 SO3(9) AH°rxn = -198 kJ SO2(g) -297 de parte a 2 500) • 03 * 2 500) 0 -578 kJ/mol 0 -248 kJ/mol 0 -495 kJ/mol 0 -396 kJ/mol 0 -792 kJ/mol Submit Request Answer Provide Feedback
Use the standard reaction enthalpies given below to determine ΔH°rxn for the following reaction: 4 SO3(g) → 4 S(s) + 6O2(g) ΔH°rxn = ? Given: SO2(g) → S(s) +O2(E) ΔH°rxn = +296.8 kJ 2 SO2(g) + O2(g) → 2SO3(g) ΔH°rxn = -197.8 kJ-494.6 kJ -692.4 kJ -791.4 kJ 1583 kJ 293.0 kJ
9.Enter your answer in the provided box. S(rhombic) + O2(g) → SO2(g) ΔHo rxn= −296.06 kJ/mol S(monoclinic) + O2(g) → SO2(g) ΔHo rxn= −296.36 kJ/mol calculate the enthalpy change for the transformation S(rhombic) → S(monoclinic) (Monoclinic and rhombic are different allotropic forms of elemental sulfur.) _______kJ/mol 10. Enter your answer in the provided box Use the following data to calculate ΔHo/f for CS2(l): C(graphite) + O2(g) → CO2(g) ΔHo rxn= −393.5 kJ/mol S(rhombic) + O2(g) → SO2(g) ΔHo rxn=...
Given: C(s) + O2(g) ---> CO2(g) ΔH = −393.5 kJ/mol S(s) + O2(g) ---> SO2(g) ΔH = −296.8 kJ/mol C(s) + 2S(s) ---> CS2(ℓ) ΔH = +87.9 kJ/mol A) Calculate the standard enthalpy change for the following reaction CS2(ℓ) + 3O2(g) ---> CO2(g) + 2SO2(g) ΔH° rxn = -1075 kJ/mol B) Using the equation and standard enthalpy change for the reaction (from part A), calculate the amount of heat produced or consumed when 3.2 mol of CS2 reacts with excess...
The standard enthalpy change for the reaction of SO3(g) with H2O(l) to yield H2SO4(aq) is ΔH∘ = -227.8 kJ .? Use the following information S(s)+O2(g)→SO2(g), ΔH∘ = -296.8kJ SO2(g)+12O2(g)→SO3(g) , ΔH∘ = -98.9kJ to calculate ΔH∘f for H2SO4(aq) (in kilojoules per mole). [For H2O(l),ΔH∘f = -285.8kJ/mol]. Express your answer using four significant figures.
5) For the reaction 2 SO2(g) + O2(g) → 2 SO3(g), if initially P(SO2) = 1.2 atm, P(O2) = 1.8 atm, and P(SO3) = 2.1 atm, calculate AG for this reaction at 25°C. The following data is valid at 25°C: AG° (kJ/mol) SO 300.4 SO3 370.4 A) -140.0 kJ/mol B)-141.3 kJ/mol C)-138.7 kJ/mol D) 1,174.7 kJ/mol E) -137.6 kJ/mol
Use the ΔH°f values provided to determine ΔH°rxn for the following reaction CH4(g) + 3 Cl2(g) → CHCl3(l) + 3 HCl(g) ΔH°rxn = ? ΔH°f (kJ/mol): -75 -134 -92 A. +662 kJ B. +117 kJ C. -151 kJ D. -335 kJ The equation that corresponds to the enthalpy of formation for NH3(g) is A. N(g) + 3H(g) → NH3(g) B. N(g) + 3/2 H2(g) → NH3(g) C. 1/2 N2(g) + 3H(g) → NH3(g) D. 1/2 N2(g) + 3/2 H2(g) →...
Calculate ΔHf°(SO3) from the following information. S(s) + O2(g) → SO2(g) ΔHrxn° = -296.8 kJ SO2(g) + 1/2 O2(g) → SO3(g) ΔHrxn° = -98.9 kJ
1.For the reaction at equilibrium 2 SO3↔ 2 SO2 + O2 (∆Horxn= 198 kJ/mol), if we increase the reaction temperature, the equilibrium will (1 point ) * No shift None of the above Question lacks sufficient information Shift to the right 2. For the equilibrium reaction 2 SO2(g) + O2(g) ↔ 2 SO3(g), ∆Horxn = -198 kJ/mol. Which one of these factors would cause the equilibrium constant to increase? (1 point ) * Add a catalyst Decrease the temperature None...
Calculate Δ G for the reaction 2 SO2 (g) + O2 (g) → 2 SO3 (g) when P of SO2 = 0.500 atm, P of O2 = 0.0100 atm, and P of SO3 = 0.100 atm. The value for Δ G^o for this reaction at 298 K is -141.6 kJ. ΔG = ???? kJ I got -160.9 kj but it is incorrect.