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Question: Calculate the \(pH\) of a buffer solution prepared by dissolving \(30g\) of \(N{a_2}C{O_3}\) in \(50...

Calculate the pHpH of a buffer solution prepared by dissolving 30g30g of Na2CO3N{a_2}C{O_3} in 500mL500mL of an aqueous solution containing 150mL150mL of 1M1M HClHCl . (Ka{K_a} for HCO3HCO_3^ - = 5.63×10115.63 \times {10^{ - 11}} )
A. 8.1978.197
B. 9.1979.197
C. 10.43710.437
D. 11.19711.197

Explanation

Solution

A buffer solution is an aqueous solution that consists of a mixture of a weak acid and its conjugate base, or vice versa. Its pHpH changes up to a very small margin, when a very small amount of a strong acid or a base is added to it. Buffer solutions are used as a means of keeping pH at a nearly constant value in a wide variety of chemical applications.

Complete step by step answer:
The reaction of the hydrochloric acid with the sodium carbonate to neutralize the corresponding base is as follows:
Na2CO3+2HCl2NaCl+H2CO3N{a_2}C{O_3} + 2HCl \to 2NaCl + {H_2}C{O_3}
The number of moles is determined by the following formula:
n=wMwn = \dfrac{w}{{{M_w}}}
Where, n=n = number of moles
w=w = weight of the given solute
Mw={M_w} = molecular weight of the given solute
Now, applying the above formula to determine the number of moles of sodium carbonate, we have:
nNa2CO3=wMw=30106=0.28{n_{N{a_2}C{O_3}}} = \dfrac{w}{{{M_w}}} = \dfrac{{30}}{{106}} = 0.28
The number of moles is also determined by the following formula:
n=M×Vn = M \times V
Where, n=n = number of moles
M=M = molarity of the solution
V=V = volume of the solution
Now, applying the above formula to determine the number of moles of hydrochloric acid, we have:
nHCl=1×1501000=0.15{n_{HCl}} = 1 \times \dfrac{{150}}{{1000}} = 0.15
Thus, after neutralization, the remaining moles of Na2CO3=0.280.15=0.13N{a_2}C{O_3} = 0.28 - 0.15 = 0.13
Thus, concentration of Na2CO3=nV=0.13(0.15+0.5)LMN{a_2}C{O_3} = \dfrac{n}{V} = \dfrac{{0.13}}{{(0.15 + 0.5)L}}M
The concentration of 0.15moles0.15moles of the salt formed after neutralization = nV=0.15(0.15+0.5)LM\dfrac{n}{V} = \dfrac{{0.15}}{{(0.15 + 0.5)L}}M
The pHpH of the buffer solution = pH=pKa+log[salt][base]pH = p{K_a} + \log \dfrac{{[salt]}}{{[base]}}
Substituting the value of the concentration of the salt and base in the above equation, we have:
pH=pKa+log[0.15][0.13]pH = p{K_a} + \log \dfrac{{[0.15]}}{{[0.13]}} ….(i)
As the value of Ka{K_a} for HCO3HCO_3^ - = 5.63×10115.63 \times {10^{ - 11}}
Hence, pKa=log(5.63×1011)=110.68=10.32p{K_a} = - \log (5.63 \times {10^{ - 11}}) = 11 - 0.68 = 10.32
Substituting the value of pKap{K_a} in equation (i), we have:
pH=10.32+log0.150.13=10.32+0.117=10.437pH = 10.32 + \log \dfrac{{0.15}}{{0.13}} = 10.32 + 0.117 = 10.437

Thus, the correct option is C. 10.43710.437.

Note: The pKap{K_a} value is one of the various methods that is used to indicate the strength of an acid. pKap{K_a} is defined as the negative log of the acid dissociation constant or Ka{K_a} value. A lower pKap{K_a}value indicates that the acid is strong in nature. This means that the lower the value of pKap{K_a} , the more of the acid dissociates in the water.