In: Chemistry
a) Calculate the pH in 0.030M H2SO3(Ka1=1.5
a)
M = 0.030 M of H2SO3
H2SO3 <-> H+ HSO3
HSO3- <-> H+ SO3-2
This will be formed...
We need the [H+] concentration
From the first equilbrium
Ka1 = [HSO3-][H+] /[H2SO3]
Ka2 = [SO3-2 ][H+]/ [HSO3-]
There will be two H+ to account, the Ka1 and form Ka2
Let us calculate first the ammount of Ka1 H+ ions
NOTE: [HSO3-] = [H+] = x since for 1 mol of [H+] you will have always another mol of HSO3-
[H2SO3] = 0.030 - x
Where x is the acid already in solution
Ka = 1.5*10^-2
Substitute in Ka1
Ka1 = [HSO3-][H+] /[H2SO3]
1.5*10^-2 = x*x / (0.030 - x )
Solve for x
x = 0.015 and -0.3
ignore the negative solution since there are no negative concentrations
x = [H+] = [HSO3-] = 0.015
Please remember this number, we will use it at the end when calculating total H+ moles
HINT: we could ignore the second equilibrium since Ka2 is too low compared to the Ka1. That is, the 95% or more of the acid is given by the first ionization
But lets do the other Ka2 equilibrium
Assume, once again
[SO3-2 ]= [H+] = y NOTE that these H+ ions are from the SECOND ionization and cannot be compared with the first ionization, thats why I'm using x and y to denote difference
[HSO3-] = x-y
[HSO3-] = x will be before the second dissociation, after the dissociation you need to account for the lost acid which is denoted as -y
Ka2 = 6.3*10^-8
Ka2 = [SO3-2 ][H+]/ [HSO3-]
Substitute all data
6.3*10^-8= y*y / (x-y)
6.3*10^-8 = y2 / (0.015-y)
Sovle for y
y = 3.07*10^-5 and -3.07*10^-5
Ignore negative values, no negative concentrations exist
Then
[H+] = y = 3.07*10^-5
Time to add [H+] of first ionization +[H+] of second ionization
that is x+y = 0.015 + 3.07*10^-5 = 0.01503
As you can see, the effect of the second ion is not enough to change the value of x significantively
pH = -log[H+] = -log(0.01503) = 1.82
pH = 1.82
B)
[H+] = 0.01503
[OH-] = 10^-14 / [H+] = (10^-14)/(0.01503) = 6.65*10^-13
[SO3-2] = y = 3.07*10^-5
[HSO3-] = x -y = 0.015 - 3.07*10^-5 = 0.01497
[H2SO3] = 0.030 - x = 0.030 - 0.015 = 0.015