What is the pH of a solution that is 0.20 M in HF and 0.40 M in NaF? [Ka = 7.2*10^-4] I know the answer is 3.44 but could someone please explain how they got it? Thank you so much!!!! (:

2 Answers
Dec 31, 2017

You get it like this:

Explanation:

HF is a weak acid which dissociates:

#sf(HFrightleftharpoonsH^(+)+F^-)#

#sf(K_a=([H^+][F^-])/([HF])=7.2xx10^(-4))#

Rearranging:

#sf([H^+]=K_axx([HF])/([F^-]))#

Putting in the numbers:

#sf([H^+]=7.2xx10^(-4)xx0.2/(0.4)=3.6xx10^(-4)color(white)(x)"mol/l")#

#sf(pH=-log[H^+]=-log(3.6xx10^(-4))=3.44)#

Dec 31, 2017

When I read this, I interpreted it as having initial concentrations of #"HF"# and #"NaF"#. From that, we would consider the following dissociation (units of #"M"#):

#"HF"(aq) rightleftharpoons "H"^(+)(aq) + "F"^(-)(aq)#

#"I"" "0.20" "" "" "0" "" "" "0.40#
#"C"" "-x" "" "+x" "" "" "+x#
#"E"" "0.20-x" "x" "" "" "0.40+x#

This would give:

#K_a = 7.2 xx 10^(-4) = (["H"^(+)]_(eq)["F"^(-)]_(eq))/(["HF"]_(eq))#

#= (x(0.40+x))/(0.20-x)#

Taking the #-log# of both sides, this can be made to look like the Henderson-Hasselbalch equation for buffers:

#-log(K_a) = -logx - log((0.40+x)/(0.20-x))#

Since #x = ["H"^(+)]#, this is really:

#"pK"_a = "pH" - log ((0.40+x)/(0.20-x))#

Or, we can then get the Henderson-Hasselbalch equation like so:

#"pH" = "pK"_a + log ((0.40+x)/(0.20-x))#

In this case, we have a #K_a# that is fairly small, so we approximate that #0.40 + x ~~ 0.40# and #0.20 - x ~~ 0.20#:

#color(blue)("pH") ~~ -log(7.2 xx 10^(-4)) + log(0.40/0.20)#

#= color(blue)(3.44)#

In homework problems and exams, you can just use the Henderson-Hasselbalch equation to begin with, as long as you know that it only works on buffers containing a weak acid and its conjugate weak base.