The correct option is A Molar concentration of weak acid is more than the concentration of strong base i.e [CH3COOH]>[NaOH]
Theory:
Condition-1 where [WA]>[SB]
CH3COOH(aq)+NaOH(aq)→CH3COONa(aq)+H2O(l)
4 3 − −
1 0 3 3
This can act as acidic buffer
Condition-2 where [WA]=[SB]
CH3COOH(aq)+NaOH(aq)→CH3COONa(aq)+H2O(l)
3 3 − −
0 0 3 3
(Complete consumption of acid and base, this is salt hydrolysis case. This is not a buffer)
Condition-3 where [WA]<[SB]
CH3COOH(aq)+NaOH(aq)→CH3COONa(aq)+H2O(l)
3 4 − −
0 1 3 3
(This is not a buffer as in this case due to high OH− we can assume that hydrolysis is not occurring. ∴(pOH)=−log[1]
In condition-1 where [WA]>[SB] is a buffer solution.
CH3COOH(aq)+NaOH(aq)→CH3COONa(aq)+H2O(l)
4 3 − −
1 0 3 3
3 moles of CH3COONa are at equilibrium:
The reaction here is CH3COONa(aq)→CH3COO−(aq)+Na+(aq)
3 − −
− 3 3
For, CH3COOH
At equilibrium, CH3COOH(aq)⇌CH3COO−(aq)+H+(aq)
1(1−α) 3+α α
Due to common ion effect, this equilibrium is pushed backward. Therefore α can be ignored.
So, 1−α≈1
∴ By addition of a small amount of H+ there is no significant change in the pH value as the equilibrium is moved backward and H+ is reduced.
Ka=[H+][X−]HX
Ka is constant.
[X−] and [HX] almost constant as α can be ignored.
[H+] has no significant change.
CH3COOH(aq)⇌CH3COO−(aq)+H+(aq)
In simple terms
If extra H+ is added to buffer (from a strong acid)
H+(aq)+CH3COO−⇌CH3COOH(aq)
Weak conjugate base (CH3COO−) neutralises the strong acid
If extra OH− is added to the buffer (from a strong base)
OH−(aq)+CH2COOH(aq)→CH3COO−(aq)+H2O
Water is formed preventing large increase in [OH−]