For a given reaction, $∆$H =35.5 kJ mol^-1 and $∆$S = 83.6JK^-1 mol^-1. The reaction is spontaneous at:
(Assume that $∆$H and $∆$S do not vary with temperature)

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 given reaction, ∆H = 35.5 kJ mol^–1 and ∆S = 83.6 J K^–1 mol^–1. The reaction is spontaneous at:
(Assume that ∆H and ∆S  do not vary with temperature)
1. T > 425K
2. All temperatures
3. T > 298K
4. T < 425K

A gas is allowed to expand in a well-insulated container against a constant external pressure of 2.5atm from an initial volume of 2.50 L to a final volume of 4.50L. The change in internal energy U of the gas in joules will be:
1. –500J
2. –505J
3. –506J
4. –508J

The heat of combustion of carbon to CO₂ is –393.5 KJ/mol. The heat changed 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. +630 KJ

The correct statement for a reversible process in a state of equilibrium is:
1. $∆$G = – 2.30RT log K
2. $∆$G = 2.30RT log K
3. $∆$G^o = – 2.30RT log K
4. $∆$G^o = 2.30RT log K

Which of the following statements is correct for the spontaneous adsorption of a gas?

Given the reaction: 
X₂O₄(l) → 2XO₂(g) 
ΔU = 2.1 kcal, ΔS = 20 cal K^–1 at 300 K 
The value of ΔG is:
1. 2.7 kcal
2. –2.7 kcal
3. 9.3 kcal
4. –9.3 kcal