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Question: A buffer solution is prepared by mixing 1 mole of HA and 1 mole of NaA into 1 L distilled water. Cal...

A buffer solution is prepared by mixing 1 mole of HA and 1 mole of NaA into 1 L distilled water. Calculate the change in pH when 25 mL of 0.20 M NaOH is added into 500mL of the buffer?

Explanation

Solution

Note that we are not given the value of pKap{K_a} hence we’ll solve this question without using the pKap{K_a} . The pH of a solution containing a weak acid (HA) and its conjugate base (NaA) can be given by the Henderson-Hasselbalch equation. This equation is given as:
pH=pKa+log([conjugate base][weak acid])pH = p{K_a} + \log \left( {\dfrac{{[{\text{conjugate base]}}}}{{[{\text{weak acid]}}}}} \right)

Complete Step By Step Answer:
The buffer solution given to us contains a weak acid (HA) and its conjugate base, A{A^ - } which come in the solution from the salt NaA. The value of pKap{K_a} is given as pKa=log(Ka)p{K_a} = - \log ({K_a}) . Ka{K_a} is the dissociation constant.
The buffer solution is prepared by 1 mol of weak acid and 1 mol of conjugate base. The dissociation of the salt NaA will be in 1:1 ratio. So the no. of moles of salt will be equal to the no. of moles of conjugate base A{A^ - } in the solution. The molarity or the concentration of the solution can be given as: c=nVc = \dfrac{n}{V}
[HA]=[A]=1  mol1L=1M[HA] = [{A^ - }] = \dfrac{{1\;mol}}{{1L}} = 1M
The volume of the stock solution taken is 500mL. The no. of moles of HA and A{A^ - } will be equal to: n=c.Vn = c.V
nHA=nA=1M×500×103L=0.50mol{n_{HA}} = {n_{{A^ - }}} = 1M \times 500 \times {10^{ - 3}}L = 0.50mol
Initially when the buffer solution isn’t added in the solution, the pH of the buffer will be equal to the pKap{K_a} of the acid. (since the concentration of acid and conjugate base is equal). Substituting in the equation we have:
pH1=pKa+log(1M1M)=pKap{H_1} = p{K_a} + \log \left( {\dfrac{{1M}}{{1M}}} \right) = p{K_a}
We are adding 25mL of the NaOH solution. The hydroxide ions will react in a 1:1 ratio with the weak acid (neutralization reaction will occur) and a conjugate base will be produced. HA(aq)+OH(aq)A(aq)+H2O(l)H{A_{(aq)}} + O{H^ - }_{(aq)} \to A_{(aq)}^ - + {H_2}{O_{(l)}}
The no. of moles of hydroxide ions added to the 500mL of the buffer solution will be equal to: nOH=0.20M×25×103L=0.0050mol{n_{O{H^ - }}} = 0.20M \times 25 \times {10^{ - 3}}L = 0.0050mol of OHO{H^ - } .
After neutralization reaction, the no. of OHO{H^ - } left in the solution will be =0mol= 0mol (since all the OHO{H^ - } ions will be utilized)
The no. of moles of HA left after addition of 25ML of NaOH solution =nHA=0.50mol0.0050mol=0.495mol= {n_{HA}} = 0.50mol - 0.0050mol = 0.495mol
nA=0.50mol+0.0050mol=0.505mol{n_{{A^ - }}} = 0.50mol + 0.0050mol = 0.505mol
The total volume of the buffer solution after addition of NaOH =Vtotal=500mL+25mL=525mL= {V_{total}} = 500mL + 25mL = 525mL
The new concentrations of weak acid and the conjugate base will be equal to:
[HA]=0.495mol525×103L=0.9429M[HA] = \dfrac{{0.495mol}}{{525 \times {{10}^{ - 3}}L}} = 0.9429M
[A]=0.505mol525×103L=0.9619M[{A^ - }] = \dfrac{{0.505mol}}{{525 \times {{10}^{ - 3}}L}} = 0.9619M
The pH of the solution according to the Henderson-Hasselbalch equation will be: pH2=pKa+log(0.9619M0.9429M)=pKa+0.00866p{H_2} = p{K_a} + \log \left( {\dfrac{{0.9619M}}{{0.9429M}}} \right) = p{K_a} + 0.00866
The change in the pH will be the difference between the two pH’s which comes as:
ΔpH=pH2pH1\Delta pH = p{H_2} - p{H_1}
ΔpH=pKa+0.00866pKa=0.00866\Delta pH = p{K_a} + 0.00866 - p{K_a} = 0.00866
This the required change in pH observed.

Note:
If the value of pKap{K_a} is given to us then the proceeding of the problem would be the same, but the value of pKap{K_a} will be substituted in the formula of pH and the change in pH is found according. The given buffer is an acidic buffer, since it is a solution of weak acid and conjugate base (salt).