2. Calculate the pH of a 0.230 M calcium acetate solution if the Ka for acetic acid is 1.8x10-5 .
3. Calculate the pH of a 0.225 M solution of H2CO3. Ka1 = 4.3x10^-7 ; Ka2 = 5.6x10^-11
4. Calculate the pH of a 0.0080 M solution of sulfuric acid. Ka2 = 1.2x10^-2
ANSWER;-
1)-calcium acetate is a weak base, a conjugate base of acetic acid, so:
Ka × Kb = KW that is
Kbacetate = Kw / Kaacetic acid =
= 10-14 / 1.8 x 10-5
= 5.376 × 10-10
In this case cweak base >>> Kb, that is the equation to use is:
[OH– ] =
=
[OH– ] = 1.2365 X 10-5
pOH = -log[OH- ]
= -log(1.2365 × 10-5) = +4.907
pH = 14.00 – pH = 14.00 – 4.907 =9.093
2)- For H2CO3, Ka1 = 4.3 x 10–7 and Ka2 = 5.6 x 10–11.
1st ionization equation: H2CO3 (aq) + H2O (l) ⇄ HCO3 – (aq) + H3O+ (aq)
2nd ionization equation: HCO3– (aq) + H2O (l) ⇄ CO3 2– (aq) + H3O+ (aq)
because Ka1 > Ka2 & Ka1 >> Kw, the primary source of H3O+ in the solution will be the 1st ionization step for H2CO3
H2CO3 (aq) + H2O (l) ⇄ HCO3 – (aq) + H3O+ (aq)
initial 0.040 M 0 0
∆ ∆ + x + x
equil (0.225–x)M x M x M
Ka = [H+] [HCO3-] / [CO2]
=4.3x10-7 = x² / (0.225-x)
Ka = 3.11 X 10-4
[H+] =3.11 X 10-4
pH = -log[H+] = -log(3.11 X 10-4 ) = +3.507
pH = +3.507
Just in case you weren't sure about that....
HCO3- <==> H+ + CO33- ..... Ka = 5.6x10-11
3.11 X 10-4....3.11 X 10-4 ..0 ...... initial
-x ................. +x .........+x .............. change
(3.11 X 10-4-x) (3.11 X 10-4+x ) x ..... equilibrium
Ka = [H+] [CO32-] / [HCO3-]
5.6x10-11 = (3.11 X 10-4+x)(x) / (3.11 X 10-4-x)
x IS VERY SMALL SO IT WILL ZERO IN + AND - TERM
THEN CALCULATE X = 5.6 X 10-11
3-
HSO4-+ H2O
H3O+ + SO42-
intial 8.0 x 10-3 8.0 x 10-3 0
change -x +x +x
equill (8.0 x 10-3 -x) (8.0 x 10-3 +x) +x
Ka = [H3O+] [SO42-] / [HSO4-]
0.0120 = [X]² / (0.0080 -X)
So [X]² = 0.0120*( 0.0080 - X)
X= 9.8 x 10-3
pH = -log [H+]
pH = -log (9.8 x 10-3)
pH = 2.00
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