What is the pH at the equivalence point when 35.0 mL of 0.20 M ammonia is titrated by 0.12M hydrochloric acid? K_b for ammonia is 1.8 xx 10^(-5)
1 Answer
Explanation:
Ammonia,
"NH"_ (3(aq)) + "HCl"_ ((aq)) -> "NH"_ 4"Cl"_ ((aq))
The two reactants react in a
In other words, you need equal numbers of moles of ammonia and of hydrochloric acid to get to the equivalence point.
Use the molarity and volume of the ammonia solution to determine how many moles of ammonia it contains
color(purple)(|bar(ul(color(white)(a/a)color(black)(c = n_"solute"/V_"solution" implies n_"solute" = c * V_"solution")color(white)(a/a)|)))
n_(NH_3) = "0.20 mol" color(red)(cancel(color(black)("L"^(-1)))) * overbrace(35.0 * 10^(-3)color(red)(cancel(color(black)("L"))))^(color(blue)("volume in liters"))
n_(NH_3) = "0.0070 moles NH"_3
This means that the hydrochloric acid solution must also contain
color(purple)(|bar(ul(color(white)(a/a)color(black)(c = n_"solute"/V_"solution" implies V_"solution" = n_"solute"/c)color(white)(a/a)|)))
You will have
V_(HCl) = (0.0070 color(red)(cancel(color(black)("moles"))))/(0.12color(red)(cancel(color(black)("mol")))"L"^(-1)) = "0.0583 L" = "58.3 mL"
The volume of the resulting solution will thus be
V_"total" = V_(NH_3) + V_(HCl)
V_"total" = "35.0 mL" + "58.3 mL" = "93.3 mL"
Now, notice that the reaction produces aqueous ammonium chloride in
If the reaction consumes
Ammonium chloride dissociates completely in aqueous solution to form ammonium cations,
"NH"_ 4 "Cl"_ ((aq)) -> "NH"_ (4(aq))^(+) + "Cl"_ ((aq))^(-)
The concentration of the ammonium cations in the resulting solution will be
["NH"_4^(+)] = "0.0070 moles"/(93.3 * 10^(-3)"L") = "0.07503 M"
The ammonium cations will hydrolyze to form hydronium cations ,
" " "NH"_ (4(aq))^(+) + "H"_ 2"O"_ ((l)) rightleftharpoons "NH"_ (3(aq)) " "+" " "H"_ 3"O"_ ((aq))^(+)
By definition, the acid dissociation constant,
K_a = (["NH"_3] * ["H"_3"O"^(+)])/(["NH"_4^(+)])
In this case, you will have
K_a = (x * x)/(0.07503 - x) = x^2/(0.07503 - x)
Now, you know that for aqueous solutions at room temperature, you have the following relationship between
color(purple)(|bar(ul(color(white)(a/a)color(black)(K_a xx K_b = K_W)color(white)(a/a)|)))
Here
K_W = 10^(-14) -> the ionization constant of water
This means that you have
K_a = K_W/K_b
K_a = 10^(-14)/(1.8 * 10^(-5)) = 5.56 * 10^(-10)
Since
0.07503 - x ~~ 0.07503
This will get you
K_a = x^2/0.07503 = 5.56 * 10^(-10)
Solve for
x = sqrt(0.07503 * 5.56 * 10^(-10)) = 6.46 * 10^(-6)
Since
["H"_3"O"^(+)] = 6.46 * 10^(-6)"M"
As you know, the pH of the solution is given by
color(blue)(|bar(ul(color(white)(a/a)"pH" = - log(["H"_3"O"^(+)])color(white)(a/a)|)))
This means that you have
"pH" = - log(6.46 * 10^(-6)) = color(green)(|bar(ul(color(white)(a/a)color(black)(5.19)color(white)(a/a)|)))
Finally, the result makes sense because neutralizing a weak base such as ammonia with a strong acid will result in the formation of the conjugate acid of the base, which will in turn cause the pH to be lower than