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.