In: Chemistry
Consider the titration of a 24.0 −mL sample of 0.100 M HC2H3O2 with 0.120 M NaOH. Determine each of the following. |
Part A the initial pH Express your answer using two decimal places.
SubmitMy AnswersGive Up Part B the volume of added base required to reach the equivalence point
SubmitMy AnswersGive Up Part C the pH at 6.00 mL of added base Express your answer using two decimal places.
SubmitMy AnswersGive Up Part D the pH at one-half of the equivalence point Express your answer using two decimal places.
SubmitMy AnswersGive Up Part E the pH at the equivalence point Express your answer using two decimal places.
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First of all, volumes will change in every case (Volume of base + Volume of acid), therefore the molarity will change as well
M = moles / volume
pH = -log[H+]
a) HA -> H+ + A-
Ka = [H+][A-]/[HA]
a) no NaOH
Ka = [H+][A-]/[HA]
Assume [H+] = [A-] = x
[HA] = M – x
Substitute in Ka
Ka = [H+][A-]/[HA]
Ka = x*x/(M-x)
1.8*10^-5 = x*x/(0.1-x)
This is quadratic equation
x =0.001332
For pH
pH = -log(H+)
pH =-log(0.001332)
pH in a = 2.87
b)
V = mmol of NaOH/ M of NaOh
mmol of NaOH = mmol of acid
mmol of acid = MV = 24*0.1 = 2.4
V = 2.4/0.120
V = 20 mL of base
c) 6 ml NaOH
This is in a Buffer Region, a Buffer is formed (weak base and its conjugate)
Use Henderson-Hassebach equations!
NOTE that in this case [A-] < [HA]; Expect pH lower than pKa
pH = pKa + log (A-/HA)
initially
mmol of acid = MV =2.4
mmol of base = MV = 6*0.12= 0.72 mmol of base
then, they neutralize and form conjugate base:
mmol of acid left = 2.4-0.72 = 1.68
mmol of conjguate left = 0 + 0.72 = 0.72 5
Get pKa
pKa = -log(Ka)
pKa = -log(1.8*10^-4) = 4.75
Apply equation
pH = pKa + log ([A-]/[HA]) =
pH = 4.75+ log (0.72/1.68 ) = 4.382
d) for half equiv ml
This is in a Buffer Region, a Buffer is formed (weak base and its conjugate)
Use Henderson-Hassebach equations!
NOTE that in this case [A-] = [HA]; Expect pH lower than pKa
pH = pKa + log (A-/HA)
from pKa = 4.75
pH = 4.75 + log(1)
pH = 4.75
d) Addition of Same quantitie of Acid/Base
This will be Hydrolisis (equilibrium of acid-base) and the weak acid/base will form an equilibrium
We will need Kb
Ka*Kb = Kw
And Kw = 10^-14 always at 25°C for water so:
Kb = Kw/Ka = (10^-14)/(1.8*10^-5) = 5.55*10^-10
Now, proceed to calculate the equilibrium
H2O + A- <-> OH- + HA
Then K equilibrium is given as:
Kb = [HA][OH-]/[A-]
Assume [HA] = [OH-] = x
[A-] = M – x
Substitute in Kb
5.55*10^-10= [x^2]/[M-x]
recalculate M:
mmol of conjugate = 20 mmol
Total V = V1+V2 = 24+20= 44
[M] = 2.4/44= 0.0545 M
5.55*10^-10 = [x^2]/[0.0545 -x]
x =0.00000547
[OH-] =0.00000547
Get pOH
pOH = -log(OH-)
pOH = -log (0.00000547) = 5.26
pH = 14-pOH = 14-5.26= 8.74