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JEE CHEMISTRY MCQ: THERMODYNAMICS

1 Hard
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Analyzing +4 | -1
Statement I Based on the following thermochemical
reactions;
HF(aq)+OH−(aq)⟶H2O(l)+F−(aq);ΔH∘=−16.4 k cal\mathrm{HF}(a q)+\mathrm{OH}^{-}(a q) \longrightarrow \mathrm{H}_2 \mathrm{O}(l)+\mathrm{F}^{-}(a q) ; \Delta H^{\circ}=-16.4 \mathrm{~k~cal}

H+(aq)+OH−(aq)⟶H2O(l),ΔH∘=−13.7 k cal\mathrm{H}^{+}(a q)+\mathrm{OH}^{-}(a q) \longrightarrow \mathrm{H}_2 \mathrm{O}(l), \Delta H^{\circ}=-13.7 \mathrm{~k~cal}

Ionisation of HF(aq)\mathrm{HF}(\mathrm{aq}) is an exothermic reaction.

Statement II Enthalpy decrease in hydration of H+(aq)\mathrm{H}^{+}(a q) and F−(aq)\mathrm{F}^{-}(a q) exceeds the ionisation enthalpy of HF(aq)\mathrm{HF}(a q).
View answer and explanation
Correct option: A
Both Statement I and Statement II are correct and
Statement II is the correct explanation of Statement I
Option A (Both Statement I and Statement II are correct and Statement II is the correct explanation of Statement I) is correct because the ionization of HF is exothermic due to the high hydration enthalpy of H+ and F- exceeding the ionization enthalpy.

More Questions from THERMODYNAMICS

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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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