For a given reaction, if ΔH = 35.5 kJ/mol and ΔS = 83.6 J/K·mol, at what temperature is the reaction spontaneous?
(Assume ΔH and ΔS remain constant with temperature.)
1. | T < 425 K | 2. | T > 425 K |
3. | All temperatures | 4. | T > 298 K |
A gas is allowed to expand in a well insulated container against a constant external pressure of 2.5 atm from an initial volume of 2.50 L to a final volume of 4.50 L. The change in internal energy U of the gas in joules will be
(1) 1136.25 J
(2) - 500 J
(3) - 505 J
(4) + 515 J
For a sample of perfect gas when its pressure is changed isothermally from pi to pf, the entropy change is given by
(1) S = nRln(pf/pi)
(2) S = nRln(pi/pf)
(3) S = nRTln(pf/pi)
(4) S = RTln(pf/pi)
The correct thermodynamic conditions for the spontaneous reaction at all temperatures is
The heat of combustion of carbon to CO2 is -393.5 kJ/mol. The heat released upon the
formation of 35.2 g of CO2 from carbon and oxygen gas is
1. -315 kJ
2. +315 kJ
3. -630 kJ
4. -3.15 kJ
For the reaction, X2O4(l) 2XO2(g)
U = 2.1 kcal, S = 20 cal K-1 at 300 K. Hence, G is
1. 2.7 kcal
2. -2.7 kcal
3. 9.3 kcal
4. -9.3 kcal
The standard enthalpy of vaporisation vapH for water at 100C is 40.66 kJ mol-1. The
internal energy of vaporisation of water at 100C (in kJ mol-1) is-
(Assume water vapour to behave like an ideal gas)
1. +37.56
2. -43.76
3. +43.76
4. +40.66
If the enthalpy change for the transition of liquid water to steam is 30 kJ mol-1 at 27°C,
the entropy change for the process would be
1. 1.0 J mol-1 K-1
2. 0.1 J mol-1K-1
3. 100 J mol-1K-1
4. 10 J mol-1K-1
1. \(\mathrm{q} \neq 0, \quad \Delta \mathrm{T}=0, \quad \mathrm{~W}=0\)
2. \(\mathrm{q}=0, \quad \Delta \mathrm{T}=0, \quad \mathrm{~W}=0\)
3. \(\mathrm{q}=0, \quad \Delta \mathrm{T}<0, \quad \mathrm{~W} \neq 0\)
4. \(\mathrm{q}=0, \quad \Delta \mathrm{T} \neq 0, \quad \mathrm{~W}=0\)
Enthalpy change for the reaction,
4H(g) 2H2(g) is -869.6 kJ
The dissociation energy of H-H bond is
1. -869.6 kJ
2. + 434.8 kJ
3. +217.4 kJ
4. -434.8 kJ