A 42.0 mL sample of 0.120 M HNO2 is titrated with 0.214 M KOH. (Ka for HNO2 is 4.57×10−4.)
Determine the pH at the equivalence point for the titration of HNO2 and KOH.
find the volume of KOH used to reach equivalence point
M(HNO2)*V(HNO2) =M(KOH)*V(KOH)
0.12 M *42.0 mL = 0.214M *V(KOH)
V(KOH) = 23.5514 mL
Given:
M(HNO2) = 0.12 M
V(HNO2) = 42 mL
M(KOH) = 0.214 M
V(KOH) = 23.5514 mL
mol(HNO2) = M(HNO2) * V(HNO2)
mol(HNO2) = 0.12 M * 42 mL = 5.04 mmol
mol(KOH) = M(KOH) * V(KOH)
mol(KOH) = 0.214 M * 23.5514 mL = 5.04 mmol
We have:
mol(HNO2) = 5.04 mmol
mol(KOH) = 5.04 mmol
5.04 mmol of both will react to form NO2- and H2O
NO2- here is strong base
NO2- formed = 5.04 mmol
Volume of Solution = 42 + 23.5514 = 65.5514 mL
Kb of NO2- = Kw/Ka = 1*10^-14/4.57*10^-4 = 2.188*10^-11
concentration ofNO2-,c = 5.04 mmol/65.5514 mL = 0.0769M
NO2- dissociates as
NO2- + H2O -----> HNO2 + OH-
0.0769 0 0
0.0769-x x x
Kb = [HNO2][OH-]/[NO2-]
Kb = x*x/(c-x)
Assuming x can be ignored as compared to c
So, above expression becomes
Kb = x*x/(c)
so, x = sqrt (Kb*c)
x = sqrt ((2.188*10^-11)*7.689*10^-2) = 1.297*10^-6
since c is much greater than x, our assumption is correct
so, x = 1.297*10^-6 M
[OH-] = x = 1.297*10^-6 M
use:
pOH = -log [OH-]
= -log (1.297*10^-6)
= 5.887
use:
PH = 14 - pOH
= 14 - 5.887
= 8.113
Answer: 8.11
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