NEET Chemistry Equilibrium / साम्यावस्था Activation energy, Standard free energy and Degree of dissociation and Vapour density

Activation energy, Standard free energy and Degree of dissociation and Vapour density

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Activation energy, Standard free energy and Degree of dissociation and Vapour density

 

Relation between vapour density and degree of dissociation.

 

In the following reversible chemical equation.

                        \[A\]   ?    \[yB\]

Initial mol          1               0

At equilibrium     (1–x)          yx                x = degree of dissociation

Number of moles of \[A\] and \[B\] at equilibrium \[=1-x+yx=1+x(y-1)\]

If initial volume of 1 mole of A is V, then volume of equilibrium mixture of \[A\] and \[B\] is, \[=[1+x(y-1)]V\]

Molar density before dissociation,  \[D=\frac{molecular\ weight}{volume}=\frac{m}{V}\]

Molar density after dissociation, \[d=\frac{m}{[1+x(y-1)]V}\]; \[\frac{D}{d}=[1+x(y-1)]\];  \[x=\frac{D-d}{d(y-1)}\]

\[y\] is the number of moles of products from one mole of reactant. \[\frac{D}{d}\] is also called Van’t Hoff factor.

In terms of molecular mass,

            \[x=\frac{M-m}{(y-1)\,m}\]; Where \[M=\] Initial molecular mass, \[m=\] molecular mass at equilibrium 

Thus for the equilibria

(I) \[PC{{l}_{5(g)}}\rightleftharpoons PC{{l}_{3(g)}}+C{{l}_{2(g)}},y=2\]

(II) \[{{N}_{2}}{{O}_{4(g)}}\rightleftharpoons 2N{{O}_{2(g)}},\ y=2\]

(III) \[2N{{O}_{2}}\rightleftharpoons {{N}_{2}}{{O}_{4}},\ y=\frac{1}{2}\]

            \[\therefore \] \[x=\frac{D-d}{d}\] (for I and II) and \[x=\frac{2(d-D)}{d}\] (for III)

Also \[D\times 2=\] Molecular weight (theoretical value)

\[d\times 2=\] Molecular weight (abnormal value) of the mixture

 

Notes - Activation energy, Standard free energy and Degree of dissociation and Vapour density


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