Consider the reversible isothermal expansion of an ideal gas in a closed system at two different temperatures $${T_1}$$ and $${T_2}$$ $$\left( {{T_1} < {T_2}} \right).$$ The correct graphical depiction of the dependence of work done $$(w)$$ on the final volume $$(V)$$ is :
A.
B.
C.
D.
Answer :
Solution :
For reversible isothermal expansion,
$$\eqalign{
& w = - nRT\ln \frac{{{V_2}}}{{{V_1}}} \cr
& \therefore \,\left| w \right| = nRT\ln \frac{{{V_2}}}{{{V_1}}} \cr
& \left| w \right| = nRT\left( {\ln \,{V_2} - \ln {V_1}} \right) \cr
& \left| w \right| = nRT\ln \,{V_2} - nRT{V_1} \cr
& y = mx + c \cr} $$
So, slope of curve 2 is more than curve 1 and intercept of curve 2 is more negative than curve 1.
Releted MCQ Question on Physical Chemistry >> Chemical Thermodynamics
Releted Question 1
The difference between heats of reaction at constant pressure and constant volume for the reaction : $$2{C_6}{H_6}\left( l \right) + 15{O_{2\left( g \right)}} \to $$ $$12C{O_2}\left( g \right) + 6{H_2}O\left( l \right)$$ at $${25^ \circ }C$$ in $$kJ$$ is
$${\text{The}}\,\Delta H_f^0\,{\text{for}}\,C{O_2}\left( g \right),\,CO\left( g \right)\,$$ and $${H_2}O\left( g \right)$$ are $$-393.5,$$ $$-110.5$$ and $$ - 241.8\,kJ\,mo{l^{ - 1}}$$ respectively. The standard enthalpy change ( in $$kJ$$ ) for the reaction $$C{O_2}\left( g \right) + {H_2}\left( g \right) \to CO\left( g \right) + {H_2}O\left( g \right)\,{\text{is}}$$