eq pt.
mL acid x M acid = mL KOH x M KOH
Solve for mL KOH.
0 mL:
.........HPr ==> H^+ + Pr^-
I......0.165.....0.....0
C.........-x......x....x
E.......0.165-x...x....x
Ka = (H^+)(Pr^-)/(HPr).
Substitute from the E line and solve for x = (H^+), then convert to pH.
For additions up to but not including eq pt use the Henderson-Hasselbalch equation.
For the eq pt the pH is determined by the hydrolysis of the salt. (salt) = (Pr^-) = (0.165 x 30 mL)/(total mL) where total mL = 30 + mL to eq pt. I will call this 0.1 M but you need to do it more accurately
........Pr^- + HOH ==> HPr + OH^-
I......0.1..............0.....0
C........-x.............x.....x
E......0.1-x............x.....x
Kb for Pr^- = (Kw/Ka for acid) = (x)(x)/(0.1-x). Solve for x = (OH^-) and convert to pH.
For all points past the eq pt it will be excess OH^-.
mols base = M x L
mols acid to eq pt = ?
excess OH^- = difference.
(OH^-) = mols OH excess/total L.
Then convert to pH.
A 30 mL sample of .165 M propanoic acid is titrated with .300M KOH. Calculate the pH at each volume of added base: 0 mL, 5 mL, 10, equivalence point, one-half equivalence point, 20 mL, 25 mL. Use calculations to make a sketch of the titration curve.
2 answers
2.8?