Respuesta :
This problem uses the relationship between Kb and the the dissociation constants which is expressed as Kw = KaKb. Calculations are as follows:
Kb = KaKb
1.00 x 10^-14 = 7.2 x 10^-4(x)
x = 1.39 x 10^-11
We now need to calculate the [OH¯] using the Kb expression:
1.39 x 10^-11 = x^2 / (0.30 - x)
The denominator can be neglected. Thus, x is 3.73 x 10^-6.
pOH = -log 3.73 x 10^-6 = 5.43
pH = 14-5.43 = 8.57
Kb = KaKb
1.00 x 10^-14 = 7.2 x 10^-4(x)
x = 1.39 x 10^-11
We now need to calculate the [OH¯] using the Kb expression:
1.39 x 10^-11 = x^2 / (0.30 - x)
The denominator can be neglected. Thus, x is 3.73 x 10^-6.
pOH = -log 3.73 x 10^-6 = 5.43
pH = 14-5.43 = 8.57
Answer:
pH=8.32
Explanation:
The relevant equilibrium for this problem is
F⁻ + H₂O ↔ HF + OH⁻
With a constant Kb of
Kb=[tex]\frac{[HF][OH^{-}]}{[F^{-}]}[/tex]
Kb=[tex]\frac{x*x}{0.30-x}[/tex]
To calculate the value of Kb we use the formula Kw=Ka*Kb, where Kw is the ionization constant of water, 1 * 10⁻¹⁴.
1 * 10⁻¹⁴ = 7.2*10⁻⁴ * Kb
Kb = 1.4 * 10⁻¹¹
So now we have
1.4 * 10⁻¹¹=[tex]\frac{x*x}{0.30-x}[/tex]
We make the assumption that x<<<0.30 M, so we can rewrite the equation of Kb as:
1.4 * 10⁻¹¹=[tex]\frac{x*x}{0.30}[/tex]
[tex]4.2*10^{-12}=x^{2} \\x=2.05*10^{-6}[/tex]
So [OH⁻]=2.05*10⁻⁶
- pOH=5.68
- pH = 14 - pOH
- pH=8.32