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Question: How would you use the Henderson-Hasselbalch equation to calculate the pH of buffer solution that is ...

How would you use the Henderson-Hasselbalch equation to calculate the pH of buffer solution that is 0.27M0.27M formic acid (HCO2H)\left( {HC{O_2}H} \right) and 0.50M0.50M in sodium formate (HCO2Na)\left( {HC{O_2}Na} \right)?

Explanation

Solution

We have to know that while calculating pHpH, we can use Henderson-Hasselbalch equation for calculating the pHpH of buffer solution and the numerical acid dissociation constant Ka{K_a} of acid that is known and by using this, we can calculate the pH for that specific solution.

Complete answer:
We can calculate the pHpH of the solution using Henderson-Hasselbalch equation. We can relate the pHpH, pKap{K_a} and molarity using Henderson-Hasselbalch equation. We have to know that equilibrium between weak acid and its conjugate base permits the solution to prevent the pH change when a certain quantity of strong acid (or) strong base is added and so, we can estimate the pH of this buffer using Henderson-Hasselbalch equation. We can write Henderson-Hasselbalch equation as,
pH=pKa+log([A][HA])pH = p{K_a} + \log \left( {\dfrac{{\left[ {{A^ - }} \right]}}{{\left[ {HA} \right]}}} \right)
Here, we can say pH is the acidity of the solution.
The negative log of Ka{K_a} is pKap{K_a}.
The concentration of acid is [HA]\left[ {HA} \right].
The concentration of conjugate base is [A]\left[ {{A^ - }} \right].
We are provided with a molarity of sodium formate as 0.50M0.50M and molarity of formic acid as 0.27M0.27M. We can use the pKap{K_a} of formic acid as 3.753.75.
Let us now substitute these values in the Henderson-Hasselbalch equation. By using these values, we can calculate the pH as follows,
pH=pK+log([A][HA])pH = pK + \log \left( {\dfrac{{\left[ {{A^ - }} \right]}}{{\left[ {HA} \right]}}} \right)
Now we can substitute the known values we get,
pH=3.75+log([0.5][0.27])pH = 3.75 + \log \left( {\dfrac{{\left[ {0.5} \right]}}{{\left[ {0.27} \right]}}} \right)
pH=3.75+0.268pH = 3.75 + 0.268
On simplification we get,
pH=4.02pH = 4.02
We have calculated the pH of the buffer solution as 4.024.02.

Note:
We have to know that the value of pH of the solution is higher when compared to the value of pKap{K_a} that represents the presence of a more conjugate base when compared to weak base. The logarithm would have position value, which indicates the value of pH would increase gradually.