You have to assume your unknown hydroxide is completely dissociate in aqueous solution. If so, then you can calculate pOH
pOH of the solution as pOH=−log[OH
−
]
pOH=−log[OHX−]. Then, pH=pK
w
−pOH=pK
w
+log
[OH
−
]
pH=pKw−pOH=pKw+log[OHX−]. Now, you see, since pK
w
=14
pKw=14, only unknown is [OH
−
]
[OHX−].
Now look at the reaction of your unknown hydroxide with lead (II) nitrate:
2OH
−
(aq)+Pb(NO
3
)
2
(aq)
⟶Pb(OH)
2
(s)+2NO
3
(aq)
2OHX−(aq)+Pb(NOX3)X2(aq)⟶Pb(OH)X2(s)+2NOX3(aq)
Since you know the precipitated amount of Pb(OH)
2
Pb(OH)X2 isolated from 1.0 L
1.0 L of unknown hydroxide solution, you can calculate original [OH
−
]
[OHX−]:
Amount of OH
−
in original solution
=3.81 g of Pb(OH)
2
×1 mol of Pb(OH)
2
241.21 g of Pb(OH)
2
×2 mol of OH
−
1 mol of Pb(OH)
2
=0.0316 mol of OH
−
Amount of OHX− in original solution=3.81 g of Pb(OH)X2×1 mol of Pb(OH)X2241.21 g of Pb(OH)X2×2 mol of OHX−1 mol of Pb(OH)X2=0.0316 mol of OHX−
Thus,[OH
−
]=0.0316 M
[OHX−]=0.0316 M, and hence,pH=pK
w
+log[OH
−
]=14+log
(0.0316)=12.5
pH=pKw+log[OHX−]=14+log(0.0316)=12.5
Asking is approximate pH
pH of orignal solution. Thus, this answer is acceptable. However, keep in mind that trace of OH
−
OHX− will remain in solution due to the solubility of Pb(OH)
2
Pb(OH)X2 in water (K
sp
=1.42×10
−20
)
(Ksp=1.42×10−20).
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