A buffer that is a mixture of acetic acid and potassium acetate has a pH = 5.22. The molar ratio of the conjugate base to weak acid in this buffer is? (acetic acid Ka = 1.8 x 10-5 )
A. 1:3
B. 1:5
C. 3:1
D. 1:1
E. 5:1
PH of buffer solution will be given as follows.
PH = PKa + log{[conjugate base]/[ACID]}
or
PH = -logKa + log{[conjugate base ]/[Acid]}
Using the both given values
5.22 = -log(1.8×10-5) +log{[conjugate base]/[Acid]}
5.22 = 4.74 + log{[conjugate base]/[Acid]}
log{[conjugate base]/[Acid]} = 5.22 - 4.74
log{[conjugate base]/[Acid] = 0.48
Taking antilog on both sides
[Conjugation base]/[Acid] = 3
Or
[Conjugation base]/[Acid] = 3/1
Or
[Conjugation base] : [Acid] = 3 : 1
Answer = C) 3 : 1
The Henderson-Hasselbalch equation for a buffer solution is given as:
pH = pKa + log([A^-]/[HA])
where pKa is the dissociation constant of the weak acid, [A^-] is the concentration of the conjugate base, and [HA] is the concentration of the weak acid.
In this case, the pH of the buffer is given as 5.22, and the dissociation constant of acetic acid is 1.8 x 10^-5. We can rearrange the Henderson-Hasselbalch equation to solve for the ratio [A^-]/[HA]:
[A^-]/[HA] = 10^(pH - pKa)
Substituting the values, we get:
[A^-]/[HA] = 10^(5.22 - (-log10(1.8 x 10^-5))) [A^-]/[HA] = 10^(5.22 + 4.74) [A^-]/[HA] = 2.39 x 10^10
This means that the ratio of [A^-] to [HA] is 2.39 x 10^10 : 1.
To simplify this ratio, we can assume that the total concentration of the buffer is 1 M (i.e., [HA] + [A^-] = 1). Then, we can write:
[A^-]/[HA] = x/1-x
where x is the molar fraction of A^- in the buffer. Substituting the ratio we found earlier, we get:
2.39 x 10^10 = x/(1-x)
Solving for x, we get:
x = 1.000000000239 x 10^-10
Therefore, the molar ratio of [A^-] to [HA] in the buffer is:
[A^-]:[HA] = x:(1-x) = 1: 9.94 x 10^9
This ratio is closest to option E, 5:1.
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