Consider a 0.10 M solution of a weak polyprotic acid (H2A) with the possible values of Ka1 and Ka2 given below. Calculate the contributions to [H3O+] from each ionization step. Ka1=1.0×10−4;Ka2=5.0×10−5

Respuesta :

Answer:

The first dissociation occurred at 0.00311 M and the second at 0.0000484 M.

Explanation:

From the given information:

The ICE table can be computed as follows:

                       H2A         →          HA⁻    +   H⁺        

Initial                0.10                      0              0

Change              -x                        x               x

Equilibrium        0.10 - x                x               x

[tex]Ka_1 = \dfrac{[HA^-][H^+]}{[H_2A]}[/tex]

[tex]1.0\times 10^{-4}= \dfrac{[x][x]}{[0.10-x]}[/tex]

[tex]1.0\times 10^{-4}= \dfrac{(x)^2}{(0.10-x)}[/tex]

By solving for x;

x² = (1.0 × 10⁻⁴ × 0.1)

x = [tex]\sqrt{1\times 10^{-5}}[/tex]

x = [H⁺] =[HA⁻] = 0.00311 M

The acid then further its dissociation again, So;

The ICE table can be computed as follows:

                         HA⁻         →          A⁻    +   H⁺        

Initial                0.00311                  0        0.00311

Change              -x                        x               x

Equilibrium      0.00311 - x             x           0.00311 + x

[tex]Ka_2 = \dfrac{[A^-][H^+]}{[HA]}[/tex]

[tex]5.0 \times 10^{-5} = \dfrac{(0.00311+x)x}{(0.00311-x)}[/tex]

By solving for x;

x = [H⁺] = 0.0000484 M

Therefore, the first dissociation occurred at 0.00311 M and the second at 0.0000484 M.