Question #672a6
1 Answer
You have to look up the
I'll use the
K_w = K_aK_b .
Therefore, you can get the
K_a = 10^(-14)/(1.3 xx 10^(-6)) = 7.69 xx 10^(-9)
The reaction itself can be denoted in general:
"BH"^(+)(aq) " "" "+" "" " "H"_2"O"(l) rightleftharpoons "H"_3"O"^(+)(aq) + "B"(aq)
"I"" ""0.10 M"" "" "" "" "" "" "-" "" "" ""0 M"" "" "" "" ""0 M"
"C"" "-x" "" "" "" "" "" "" "-" "" "+x" "" "" "" "+x
"E"" "(0.10 - x)"M"" "" "" "" "-" "" ""x M"" "" "" "" ""x M"
And its
K_a = x^2/(0.10 - x)
However, since
K_a ~~ x^2/(0.10)
Therefore, we can solve for the equilibrium concentration of
["H"_3"O"^(+)] = x ~~ sqrt(0.10K_a)
= 2.77 xx 10^(-5) "M"
Hence, the
color(blue)("pH") = -log["H"_3"O"^(+)]
= color(blue)(4.56)
And another way to check whether the small
%"dissoc". = x/(["soln"])
= (2.77 xx 10^(-5) "M")/("0.10 M") xx 100% = 0.028% "<<" 5%
So this approximation works extremely well. You would get pretty much the same answer if you chose to solve the quadratic equation in full.