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JEE CHEMISTRY MCQ: THERMODYNAMICS

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Application +4 | -1
The standard state Gibbs free energies of formation of CC (graphite) and C (diamond) at T=298 KT=298 {~K} are

ΔfG∘[C (graphite) ]=0 kJ mol−1ΔfG∘[C (diamond) ]=2.9 kJ mol−1\begin{aligned} & \Delta_f G^{\circ}[{C} \text { (graphite) }]=0 {~kJ} {~mol}^{-1} \\ & \Delta_f G^{\circ}[{C} \text { (diamond) }]=2.9 {~kJ} {~mol}^{-1} \end{aligned}

The standard state means that the pressure should be 1 bar, and substance should be pure at a given temperature. The conversion of graphite [C(graphite)] to diamond [C\left[C\right. (diamond)] reduces its volume by 2×10−6 m3 mol−12 \times 10^{-6} {~m}^3 {~mol}^{-1}. If C{C} (graphite) is converted to C{C} (diamond) isothermally at T{T} =298 K=298 {~K}, the pressure at which C{C} (graphite) is in equilibrium with C{C} (diamond), is :

[Useful information:[\text{Useful information:} 1 J=1 kg m2 s−21 {~J}=1 {~kg} {~m}^2 {~s}^{-2};
1 Pa=1 kg m−1 s−2;1bar=105 Pa]\left.1 {~Pa}=1 {~kg} {~m}^{-1} {~s}^{-2} ; 1 {bar}=10^5 {~Pa}\right]
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Correct option: A
14501 bar
Option A (14501 bar) is correct because it is the pressure calculated using the Gibbs free energy change and volume change for the conversion of graphite to diamond.

More Questions from THERMODYNAMICS

Practice All Chapter MCQs →
Consider following reactions
I:  C(s)+12O2( g)−CO(g),ΔH1=a\ \mathrm{C}(\mathrm{s})+\frac{1}{2} \mathrm{O}_2(\mathrm{~g})-\mathrm{CO}(\mathrm{g}), \Delta \mathrm{H}_1=\mathrm{a}

II: CO(g)+12O2( g)−CO2( g),ΔH2=b\mathrm{CO}(\mathrm{g})+\frac{1}{2} \mathrm{O}_2(\mathrm{~g})-\mathrm{CO}_2(\mathrm{~g}), \Delta \mathrm{H}_2=\mathrm{b}

III: C(s)+CO2( g)−2CO(g);ΔH3=c\mathrm{C}(\mathrm{s})+\mathrm{CO}_2(\mathrm{~g})-2 \mathrm{CO}(\mathrm{g}) ; \Delta \mathrm{H}_3=\mathrm{c}
Select the correct statement
When 0.18 g0.18 \mathrm{~g} of glucose was burnt in a bomb calorimeter, the temperature rose by 4 K.4 \mathrm{~K}. The heat capacity of the calorimeter system is (ΔCH∘=−2.8×106 J/mol glucose)\left(\Delta_{\mathrm{C}} \text{H}^{\circ}=-2.8\times 10^6 \mathrm{~J} / \mathrm{mol} \text{ glucose}\right) Statement-1: CsI{CsI} is less soluble in water compared to CsCl{CsCl}
Satement-2: More amount of heat is liberated during the formation of CsCl{CsCl} than the formation CsI{Cs} I from their elements
Consider the following processes :

ΔH(KJ/mol)1/2A→B+1503B→2C+D−125E+A→2D+350\begin{array}{cccccccccccccccccccc} {}&{\Delta H(KJ/mol)} \\ {1/2A \to B}&{ + 150} \\ {3B \to 2C + D}&{ - 125} \\ {E + A \to 2D}&{ + 350} \end{array}

For B+D→E+2C,ΔH{B}+{D} \rightarrow {E}+2 {C}, \Delta {H} will be :
The difference b/w ΔH\Delta H and Δu\Delta u at constant volume is equal to The heat evolved in the combustion of methane is given by the following equations CH4(g)+2O2(g)→CO2(g)+H2O(l);ΔH=−890.3kJ\mathrm{C}{\mathrm{H}_4}\left( \mathrm{g} \right) + 2{\mathrm{O}_2}\left( \mathrm{g} \right) \to \mathrm{C}{\mathrm{O}_2}\left( \mathrm{g} \right) + {\mathrm{H}_2}\mathrm{O}\left( l \right);\Delta H = - 890.3\mathrm{kJ} How many grams of methane would be required to produce 44.15 kJ of heat of combustion?
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