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JEE CHEMISTRY MCQ: THERMODYNAMICS

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Application +4 | -1
2.56 g2.56 \mathrm{~g} of sulphur is burnt in a constant volume calorimeter with excess of O2(g)\mathrm{O}_2(g). Temperature increases from 21.25∘C21.25^{\circ} \mathrm{C} to 26.72∘C26.72^{\circ} \mathrm{C}. The bomb has a heat capacity of 923 J K−1923 \mathrm{~J} \mathrm{~K}^{-1}. Calorimeter contains 815 g815 \mathrm{~g} of water. Thus, change in internal energy per mole of SO2\mathrm{SO}_2 formed for the reaction is

S8(s)+8O2(g)⟶8SO2(g)\mathrm{S}_8(s)+8 \mathrm{O}_2(g) \longrightarrow 8 \mathrm{SO}_2(g)

(Specific heat of water is 4.184 J K−1 g−14.184 \mathrm{~J} \mathrm{~K}^{-1} \mathrm{~g}^{-1} )
View answer and explanation
Correct option: A
−296.27 kJ-296.27 \mathrm{~kJ}
Option A (-296.27 kJ) is correct because the change in internal energy per mole of SO2 formed is calculated using the heat capacity of the calorimeter and the specific heat of water.

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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