Respuesta :
In the first dissociation of H2A:
molarity H2A(aq)↔ (HA)^-(aq) + H^+(aq)
initial 0.05 m 0 m 0 m
change -x +x +x
equilibrium 0.05-x x x
we can neglect X in [H2A] as it so small compared to the 0.05
so by substitution in Ka equation:
Ka1 = [HA][H] / [H2A]
2.2x10^-6 = X^2/0.05
X = √(2.2x10^-6)*(0.05)= 1.1x10^-7
X= 3.32x10^-4 m
∴ [H2A] = 0.05 - 3.32x10^-4 = 0.0497 m
[HA] = 3.32x10^-4 m
[H] = 3.32x10^-4 m
the second dissociation of H2A: when ka2 = 8.2x10^-9
HA-(aq) ↔ A^2- (aq) + H+(aq)
at equilibrium 3.32x10^-4 y 3.32x10^-4
Ka2 = [H+][A^2-] / [HA]
8.2x10^-9 = Y(3.32x10^-4)/(3.32x10^-4)
∴y = 8.2x10^-9 m
∴[A] = 8.2x10^-9 m
PH= -㏒[H+]
= -㏒(3.32x10^-4)= 3.479
[A]=8.2x10^-9 m
[H2A] = 0.0497 ≈ 0.05 m
molarity H2A(aq)↔ (HA)^-(aq) + H^+(aq)
initial 0.05 m 0 m 0 m
change -x +x +x
equilibrium 0.05-x x x
we can neglect X in [H2A] as it so small compared to the 0.05
so by substitution in Ka equation:
Ka1 = [HA][H] / [H2A]
2.2x10^-6 = X^2/0.05
X = √(2.2x10^-6)*(0.05)= 1.1x10^-7
X= 3.32x10^-4 m
∴ [H2A] = 0.05 - 3.32x10^-4 = 0.0497 m
[HA] = 3.32x10^-4 m
[H] = 3.32x10^-4 m
the second dissociation of H2A: when ka2 = 8.2x10^-9
HA-(aq) ↔ A^2- (aq) + H+(aq)
at equilibrium 3.32x10^-4 y 3.32x10^-4
Ka2 = [H+][A^2-] / [HA]
8.2x10^-9 = Y(3.32x10^-4)/(3.32x10^-4)
∴y = 8.2x10^-9 m
∴[A] = 8.2x10^-9 m
PH= -㏒[H+]
= -㏒(3.32x10^-4)= 3.479
[A]=8.2x10^-9 m
[H2A] = 0.0497 ≈ 0.05 m
At equilibrium, the pH of the solution is 3.48; [H2A] = 0.0496 and [A2-] = 8.2 × 10^-9 M
First ionization
H2A <----> H+ + HA- ;Ka1 = 2.2 × 10^-6
Ka1 = 2.2x10^-6 = [H+][HA-]/[H2A]
At equilibrium:
- [H+] = X
- [HA-] = X
- [H2A] = 0.05 - X
Substituting in the equation of Ka1
2.2 × 10^-6 = X^2/0.050 - X
- Assuming X is small relative to 0.050, 0.050 - X simplifies to 0.050
X^2 = 1.1 × 10^-7
X = 3.31 × 10^-4
Since Ka1 <<< Ka2 and [H+] = X
[H+] = 3.31 × 10^-4
pH = - log 3.31 × 10^-4
pH = 3.48
Equilibrium concentration of H2A
[H2A] = 0.05 - 3.31 × 10^-4
[H2A] = 0.0496
Second ionization:
HA- <------> H+ + A- Ka2 = 8.2 × 10^-9
Ka2 = 8.2 × 10^-9 = [H+][A2-]/[HA-]
HA- ------> H+ + A2-
3.31 × 10^-4 3.31 × 10^-4 0 Initial
-y +y +y Change
{3.31 ×10^-4 -y} {3.31 x10^-4+y} {+y} Equilibrium
Assuming y is very small:
- {3.31 ×10^-4 - y} simplifies to 3.31 ×10^-4
- {3.31 ×10^-4 + y} simplifies to 3.31 ×10^-4
Substituting in the equation of Ka2
8.2 × 10^-9 = (3.31x10^-4) × y /3.31 ×10^-4
y = 8.2 × 10^-9
Equilibrium concentration of A2-
Since [A2-] = y
[A2-] = 8.2 × 10^-9 M
Therefore, at equilibrium, the pH of the solution is 3.48; [H2A] = 0.0496 and [A2-] = 8.2 × 10^-9 M
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