Change in entropy is negative for:

1. Bromine (l)$\to$Bromine(g)

2. C(s) + H₂O(g) $\to$CO(g) + H₂(g)

3. N₂(g,10 atm)$\to$N₂(g,1 atm) 

4. Fe ( 1mol, 400 K) $\to$ Fe( 1mol, 300 K)

For the following given equations and $∆\mathrm{H}°$ values, determine the enthalpy of reaction at 298 K for the reaction:

C₂H₄(g) + 6F₂(g) $\to$ 2CF₄(g) + 4HF(g)

H₂(g) + F₂(g) $\to$ 2HF(g)       $∆{\mathrm{H}}_1^{°}$= -537 kJ

C(s) + 2F₂(g) $\to$CF₄(g)         $∆{\mathrm{H}}_2^{°}$=-680 kJ

2C(s) + 2H₂(g) $\to$C₂H₄(g)    $∆{\mathrm{H}}_3^{°}$= 52 kJ

1. –1165 kJ

2. –2486 kJ

3. +1165 kJ

4. +2486 kJ

Entropy decreases during:

1. Crystallization of sucrose from solution

2. Rusting of iron

3. Melting of ice

4. Vaporization of camphor

A piston filled with 0.04 mol of an ideal gas expands reversibly from 50.0 mL to 375 mL at a constant temperature of 37.0ºC. As it does so, it absorbs 208 J of heat. The values of q and w for the process will be-
(R = 8.314 J/mol K) (ln 7.5 = 2.01)

$∆{\mathrm{H}}_{\mathrm{f}}^0$ (298K) of methanol is given by the chemical equation:

1. \(\mathrm{C}(\text { diamond })+\frac{1}{2} \mathrm{O}_{2(\mathrm{~g})}+2 \mathrm{H}_{2(\mathrm{~g})} \rightarrow \mathrm{CH}_3 \mathrm{OH}_{(\mathrm{l})}\)

2. \(\mathrm{CH}_{4(\mathrm{~g})}+\frac{1}{2} \mathrm{O}_{2(\mathrm{~g})} \rightarrow \mathrm{CH}_3 \mathrm{OH}_{(\mathrm{g})}\)

3. \(\mathrm{CO}_{(\mathrm{g})}+2 \mathrm{H}_{2(\mathrm{~g})} \rightarrow \mathrm{CH}_3 \mathrm{OH}_{(\mathrm{l})}\)

4. \(\mathrm{C}(\text { graphite })+\frac{1}{2} \mathrm{O}_{2(\mathrm{~g})}+2 \mathrm{H}_{2(\mathrm{~g})} \rightarrow \mathrm{CH}_3 \mathrm{OH}_{(\mathrm{l})}\)

When 4 g of iron is burnt to ferric oxide at a constant pressure, 29.28 kJ of heat is evolved.

The enthalpy of formation of ferric oxide will be-

(At. mass of Fe = 56) ?

1. $-$81.98 kJ

2. $-$ 819.8 kJ

3. $-$ 40.99 kJ

4.  +819.8 kJ

The entropy change in the isothermal reversible expansion of 2 moles of an ideal gas from 10 to 100 L at 300 K is

1. $42.3<mspace\; width="1em"></mspace>\mathrm{J}<mspace\; width="1em"></mspace>{\mathrm{K}}^{-1}$

2. $35.8<mspace\; width="1em"></mspace>\mathrm{J}<mspace\; width="1em"></mspace>{\mathrm{K}}^{-1}$

3. $38.3<mspace\; width="1em"></mspace>\mathrm{J}<mspace\; width="1em"></mspace>{\mathrm{K}}^{-1}$

4. $32.3<mspace\; width="1em"></mspace>\mathrm{J}<mspace\; width="1em"></mspace>{\mathrm{K}}^{-1}$

As an isolated box, equally partitioned, contains two ideal gasses A and B as shown:

When the partition is removed, the gases mix. The changes in enthalpy $(∆\mathrm{H})$ and entropy $(∆\mathrm{S})$ in the process, respectively, are

1. Zero, positive

2. Zero, negative

3. Positive, zero

4. Negative, zero

Hydrolysis of sucrose is given by the following reaction

Sucrose + H₂O $\rightleftharpoons$ Glucose + Fructose

If the equilibrium constant (K_c) is 2$\times$10¹³ at 300 K, the value of ${∆}_r{G}^{⊝}$ at the same temperature will be:

1. 8.314 J mol^–1 K^–1$\times$300 K$\times$ln (2$\times$10¹³)

2. 8.314 J mol^–1 K^–1$\times$300 K$\times$ln (3$\times$10¹³)

3. –8.314 J mol^–1 K^–1$\times$300 K$\times$ln (4$\times$10¹³)

4. –8.314 J mol^–1 K^–1$\times$300 K$\times$ln (2$\times$10¹³)

What is the value of ∆H for the reaction 2Al + Cr₂O₃ → 2Cr + Al₂O₃, knowing that the enthalpies of
formation of Al₂O₃ and Cr₂O₃ are –1596 kJ and –1134 kJ, respectively?