A buffer solution is to be made using 1.00 mol dm–3 ethanoic acid, CH3CO2H, and
1.00 mol dm–3 sodium ethanoate, CH3CO2Na.
Calculate to the nearest 1 cm3 the volumes of each solution that would be required to
make 100 cm3 of a buffer solution with pH 5.50.
Clearly show all steps in your working.
Ka (CH3CO2H) = 1.79 × 10–5 mol dm–3
Answer.
Putting pH and pKa in the Handerson-Hassalbach Equation we will get [A]/[HA] = 0.753..... Now to calulate the volume i want to use c = n / v; c = 1 M but no clue where to find the number of moles ??
Originally posted by hoay:A buffer solution is to be made using 1.00 mol dm–3 ethanoic acid, CH3CO2H, and
1.00 mol dm–3 sodium ethanoate, CH3CO2Na.
Calculate to the nearest 1 cm3 the volumes of each solution that would be required to
make 100 cm3 of a buffer solution with pH 5.50.
Clearly show all steps in your working.Ka (CH3CO2H) = 1.79 × 10–5 mol dm–3
Answer.
Putting pH and pKa in the Handerson-Hassalbach Equation we will get [A]/[HA] = 0.753..... Now to calulate the volume i want to use c = n / v; c = 1 M but no clue where to find the number of moles ??
okay i got it. V= 43 cm3
Originally posted by hoay:okay i got it. V= 43 cm3
A buffer solution is titrated with NaOH(aq). Upon addition of 3 volumes of NaOH(aq), the buffer solution becomes most effective. Equivalence point is attained when 8 volumes of NaOH(aq) is added.
a) Calculate the ratio of the molarities of both members of the conjugate acid-base pair of the buffer solution, before the NaOH(aq) is added.
b) Given that the original pH of the buffer solution (ie. before NaOH(aq) is added) is 4.16, calculate the proton dissociation constant of the acidic component of the buffer.
Solution :
a) At maximum buffer capacity :
HA + OH- ---> A- + H2O
Initial (mol) 8y 3y x-8y n.a.
Change (mol) -3y -3y +3y n.a
Final (mol) 5y 0 x-5y n.a.
At equivalence point :
HA + OH- ---> A- + H2O
Initial (mol) 8y 8y x-8y n.a.
Change (mol) -8y -8y +8y n.a.
Final (mol) 0 0 x n.a.
First, complete the ICF table for equivalence point. Next, complete the ICF table for maximum buffer capacity, bearing in mind that the initial moles of HA and A- are the same (for both tables).
Since at maximum buffer capacity, [HA] = [A-], this implies 5y = x-5y and hence x = 10y.
Substituting x = 10y into the initial moles of A-, we have moles of A- = 2y.
Therefore, the ratio of the amounts of both members of the conjugate acid-base pair present in the buffer (before NaOH(aq) is added), is 8y HA : 2y A-, ie. 4 HA : 1 A-
b) Using the Henderson-Hasselbalch equation, we have
pH = pKa + log ( [base] / [acid] )
4.16 = pKa + log (1/4)
pKa = 4.762
Ka = 1.73 x 10^-5