9 . sol:-
(a)
First deprotonation of H2SO4 is :
H2SO4(aq) ------------------> H+(aq) + HSO4-(aq)
second deprotonation of H2SO4 will be partial because it is more difficult to remove one hydrogen from an anion i.e HSO4-(aq) as :
HSO4-(aq) <-----------------> H+(aq) + SO42-(aq) , ka = 1.2 X 10-2 (given )
(b)
after the first deprotonation the concentration of HSO4- and H+ are equal to concentration of H2SO4 i.e 0.0456 M , because H2SO4 is the strong dibasic acid and therefore its first deprotonation or dissociation will be complete i.e H2SO4 has very high value of dissociation constant ( ka).
H2SO4(aq) ------------------> H+(aq) + HSO4-(aq)
0.0456 M 0.0456 M 0.0456 M
Hence, [H+] = 0.0456 M
and [HSO4-] = 0.0456 M
(c)
concentration of SO42- and H+ after the second deprotonation can be calculated by using ICE table .
because ,value of ka for HSO4- is small , therefore its dissociation will be partial as :
HSO4-(aq) <-----------------> H+(aq) + SO42-(aq) , ka = 1.2 X 10-2 (given )
I 0.0456 M 0.0456 M 0
C -x +x +x
E (0.0456 - x) M (0.0456 + x ) M x M
Now , the expression of ka for HSO4- will be :
ka =[ H+] [ SO42-] / [ HSO4-]
1.2 X 10-2 = (0.0456 +x ) x /(0.0456 - x)
on cross multiplication , we have
1.2 X 10-2 (0.0456 - x) = (0.0456 +x)x
5.47 X 10-4 - 0.012x = 0.0456x + x2
as x is very very small , therefore neglect x2
0.0456x + 0.012x = 5.47 X 10-4
0.0576x = 5.47 X 10-4
x = 5.47 X 10-4 / 0.0576
x = 0.0095
hence , [ SO42-] = x = 0.0095 M
and [ H+] = 0.0456 + x = 0.0456 + 0.0095 = 0.055 M
(d)
From first dissociation , we have [ H+ ] = 0.0456 M
because pH = - log [ H+]
therefore , pH = - log 0.0456
pH = - ( - 1.34 )
pH = 1.34
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