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1.
How will you calculate the work done on an ideal gas in a compression, when change in pressure is carried out in infinite steps?
2.
Standard molar enthalpy of formation, \({ \Delta }_{ f }{ H }^{ o }\) is just a special case of enthalpy of reaction, \({ \Delta }_{ r }{ H }^{ o }\). Is the \({ \Delta }_{ f }{ H }^{ o }\) for the following reaction same as \({ \Delta }_{ f }{ H }^{ o }\) ? Give reason for your answer.
CaO(s) + CO2(g)\(\longrightarrow \)CaCO3(s);
\({ \Delta }_{ f }{ H }^{ o }=-178.3 \ kJ \ { mol }^{ -1 }\)
3.
The value of \({ \Delta }_{ f }{ H }^{ \Theta }\) for NH3 is -91.8 kJ mol-1. Calculate enthalpy change for the following reaction.
\(2{ NH }_{ 3 } \ (g)\longrightarrow { N }_{ 2 }(g) \ + \ { 3H }_{ 2 }(g)\)
4.
Although heat is path function but heats absorbed by the system under certain specific conditions is independent of path. what are those conditions? Explain when pressure remains constant.
5.
Although heat is path function but heats absorbed by the system under certain specific conditions is independent of path. what are those conditions? Explain when volume remains constant.
1.
When compression is carried out in infinite steps with change in pressure, it is a reversible process. Work done on the gas is represented by the shaded area.

2.
The standard enthalpy change for the formation of one mole of a compound from its elements in their most stable states (reference states) is called standard molar enthalpy of formation, \({ \Delta }_{ f }{ H }^{ o }\) .
\(Ca(s)+C(s)+\frac { 3 }{ 2 } { O }_{ 2 }(g)\longrightarrow Ca{ CO }_{ 3 }(s);{ \Delta }_{ f }{ H }^{ o }\)
This reaction is different from the given reaction.
Hence, \({ \Delta }_{ r }{ H }^{ o }\neq { \Delta }_{ f }{ H }^{ o }\)
3.
Given, \(\frac { 1 }{ 2 } { N }_{ 2 }(g)+{ \frac { 3 }{ 2 } }{ H }_{ 2 }(g)\longrightarrow { NH }_{ 3 }(g);\)
\({ \Delta }_{ f }{ H }^{ \Theta }=-91.8 \ kJ \ { mol }^{ -1 }\)
(\({ \Delta }_{ f }{ H }^{ \Theta }\) means enthalpy of formation of 1 mole of NH3)
\(\therefore\) Enthalpy change for the formation of 2 moles of NH3
\({ N }_{ 2 }(g)+{ 3H }_{ 2 }(g)\rightarrow { 2NH }_{ 3 }(g);\)
\({ \Delta }_{ f }{ H }^{ \Theta }=2\times -91.8=-183.6 \ kJ \ { mol }^{ -1 }\)
And for the reverse reaction. \(2{ NH }_{ 3 }(g)\longrightarrow { N }_{ 2 }(g)+{ 3H }_{ 2 }(g);{ \Delta }_{ f }{ H }^{ \Theta }=+183.6 \ kJ \ { mol }^{ -1 }\) Hence, the value of \({ \Delta }_{ f }{ H }^{ \Theta }\) for NH3 is +183.6 kJ mol-1
4.
At constant pressure \(q_{ p }=\triangle U+p\triangle V.\)
But \(\triangle U+p\triangle V=\triangle H\).
\(\therefore \ q_{ p }=\triangle H\). As \(\triangle H\) is a state function, therefore, \(q_{ p }\) is a state function.
5.
At Constant volume By first law of thermodynamics, \(\triangle U=q+W \ or \ q=\triangle U-W.\)But \(W=-p\triangle V.\) Hence, \(q=\triangle U+p\triangle V.\) But as volume remains constant, \(\triangle V=0\) .
\(\therefore qV=\triangle U\). But \(\triangle U\) is state function. Hence, \(q_{ v }\) is state function.
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