Question #e9b66
1 Answer
Here's what I got.
Explanation:
A generic weak acid
#"HA"_ ((aq)) rightleftharpoons "H"_ ((aq))^(+) + "A"_ ((aq))^(-)#
Now, the acid dissociation constant,
#K_a = (["H"^(+)] * ["A"^(-)])/(["HA"])#
Now, the
#color(blue)(ul(color(black)("p"k_a = - log(K_a))))#
Plug the expression you have for the acid dissociation constant into the expression you have for the
#"p"K_a = - log ((["H"^(+)] * ["A"^(-)])/(["HA"]))#
This can be written as
#"p"K_a = - log ( ["H"^(+)] * (["A"^(-)])/(["HA"]))#
which, in turn, is equivalent to
#"p"K_a = -[ log(["H"^(+)]) + log((["A"^(-)])/(["HA"]))]#
#"p"K_a = - log(["H"^(+)]) - log((["A"^(-)])/(["HA"]))#
At this point, you should recognize that
#color(blue)(ul(color(black)("pH" = - log(["H"^(+)]))#
This means that you have
#"p"K_a = "pH" - log((["A"^(-)])/(["HA"]))#
which is equivalent to
#color(red)(ul(color(black)("pH" = "pK"_a + log((["A"^(-)])/(["HA"]))))) -># the Henderson - Hasselbalch equation
This equation can be used to calculate the pH of a buffer solution, which, as you know, contains a weak acid and its conjugate base or a weak base and its conjugate acid in comparable amounts.
Now, notice what happens when
#ul(["A"^(-)] = ["HA"])#
In this case, you have
#(["A"^(-)])/(["HA"]) = 1" "# and#" " log((["A"^(-)])/(["HA"])) = log(1) = 0#
This will get you
#"pH" = "p"K_a#
The
#ul(["A"^(-)] > ["HA"])#
In this case, you have
#(["A"^(-)])/(["HA"]) > 1" "# and#" "log((["A"^(-)])/(["HA"])) > 0#
This will get you
#"pH" = "p"K_a + "something positive"#
which implies that
#"pH" > "p"K_a#
In this case, the
#ul(["A"^(-)] < ["HA"])#
In this case, you have
#(["A"^(-)])/(["HA"]) < 1" "# and#" "log((["A"^(-)])/(["HA"])) < 0#
This will get you
#"pH" = "p"K_a + "something negative"#
which implies that
#"pH" < "p"K_a#
In this case, the