C=0.05MpKa=4.74
⇒pKa=−logKa
Ka=1.82×10−5
Ka=C∝2;∝=√KaC
∝=√1.82×10−55×10−2=1.908×10−2
When HCl is added to the soln, the concn of H+ ions will increase. Therefore, the equilibrium will shift in the backward direction, ie; dissociation of acetic acid will decrease.
Case (a) When 0.01M HCl taken
CH3COOH⟷H++CH3COO−
initial eqn 0.05 O O
0.05−x 0.01+x x
as the dissociation of a very small amount of CH3COOH will take place , the values 0.05−x and 0.01+x cn be taken as 0.05 and 0.01 respectively.
Ka=[CH3COO−][H+][CH3COOH]
∴ , Ka=(0.01x)0.05
x=1.82×10−5×0.050.01=1.82×10−3×0.05M
Now,
ρ=amountofaciddissociatedamountofacidtaken
=1.82×10−3×0.050.05
ρ=1.82×10−3M
Case (b): When 0.1M of HCl taken
[CH3COOH]=0.05−X; 0.05M
[CH3COO−]=X
[H+]=0.1+X; 0.1M
Ka=0.1X0.05
X=1.82×10−5×0.050.1
X=1.82×10−4×0.05M
So, ρ=1.82×10−4×0.050.05
ρ=1.82×10−4M