- A${K_c} = {K_p}\,{(RT)^{\Delta n}}$
- ✓${K_p} = {K_c}{(RT)^{\Delta n}}$
- C${K_p} = {\left( {\frac{{{K_c}}}{{RT}}} \right)^{\Delta n}}$
- D${K_p} - {K_c} = {(RT)^{\Delta n}}$
$aA _{( g )}+ bB _{( g )} \rightleftharpoons cC _{( g )}+ dD _{( g )}$
Let $p _{ A }, p _{ B }, p _{ C }$ and $p _{ D }$ be the partial pressure of $A , B , C$ and $D$ repectively. Therefore,
$K _{ c }=\frac{[ C ]^{ c }[ D ]^{ d }}{[ A ]^{ a }[ B ]^{ b }} \ldots . .(1)$
$K _{ p }=\frac{ pC ^c p _{ D }^{ d }}{ p _{ A }^{ a } p _{ B }^{ b }} \ldots \ldots .(2)$
For an ideal gas-
$PV = nRT$
$\Rightarrow P =\frac{ n }{ V } RT = CRT$
Whereas $C$ is the concentration.
Therefore,
$p _{ A }=[ A ] RT$
$p _{ B }=[ B ] RT$
$p _{ C }=[ C ] RT$
$p _{ D }=[ D ] RT$
Substituting the values in equation $(2),$ we have
$K _{ p }=\frac{[ C ]^{ c }( RT )^{ c }[ D ]^{ d }( RT )^{ d }}{[ A ]^{ a }( RT )^{ a }[ B ]^{ b }( RT )^{ b }}$
$\Rightarrow K _{ p }=\frac{[ C ]^{ c }[ D ]^{ d }}{[ A ]^{ a }[ B ]^{ b }}( RT )^{[( c c )-( a + b )]}$
$\left.\Rightarrow K _{ p }= K _{ c }( RT )^{\Delta n_{ g }} \quad \text { (From (1) }\right]$
Here,
$\Delta n _{ g }=$ Total no. of moles of gaseous product $-$ Total no. of moles of gaseous reactant
Hence the relation between $K_p$ and $K_c$ is-
$K _{ p }= K _{ c }( RT )^{\Delta n _{ g }}$
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$[Figure]$ $\longrightarrow \,\,A\,\xrightarrow{{{C_6}{H_5}N{H_2}}}B$


$(I)$ It is easier to remove $2 \mathrm{p}$ electron than $2 \mathrm{s}$ electron
$(II)$ $2 \mathrm{p}$ electron of $\mathrm{B}$ is more shielded from the nucleus by the inner core of electrons than the $2 s$ electrons of $Be.$
$(III)\; 2 s$ electron has more penetration power than $2 \mathrm{p}$ electron.
$(IV)$ atomic radius of $\mathrm{B}$ is more than $\mathrm{Be}$
(Atomic number $\mathrm{B}=5, \mathrm{Be}=4$ )
The correct statements are