PH of 0.60M H2SO3
H2SO3 ========== H+ + HSO3- Ka1= 1.5*10^-2
HSO3- ========== H+ + SO3-- Ka2 = 6.3*10^-8
Because the Ka1 and Ka2 are so different need do only the first dissociation. The H+ formed from the second equilibrium ek ne depressed by that formed in the first.
[H+] from second dissociation will approximately equal to Ka2 (6.6*10^-8) , so it is negligible.
H2SO3 ========== H+ + HSO3-
Initially 0.60M 0 0
equilibrium (0.60-x) x x
Ka1=[H+] [HSO3-] / [H2SO3]
1.5*10^-2 = X * X / (0.60-x)
x2 = { (1.5 * 10^-2) * 0.60 }
x= (90 * 10^-4 ) ^½
X= [H+] = 9.49*10^-2 M
pH= -log [H+]
pH= - ( log 9.49 + log 10^-2)
pH= - ( 0.98 + (-2 log 10)
pH= - ( 0.98 -2)
pH= 1.02
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