pH will be 11.51 or very close to it.
Kb=[NH4+]*[OH-]/[NH3]
[NH4+] = [OH-] = x
[NH3] = 0.6 M - x
x << 0.6 M thus [NH3] = 0.6 M
this leaves us with:
Kb = x*x/0.6
Kb = 1.77e-5
x = sqroot( 1.77e-5 * 0.6) = 0.0032
pH = 14 - log[OH-] = 14 - 2.49 = 11.51
2006-09-06 10:50:58
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answer #1
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answered by Tib 2
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You need the Ka value for ammonia, which in solution forms:
NH3 + H2O ===> NH4+ + OH-
So, ammonia gas in solution forms ammonium ion (NH4+) and hydroxide ion (OH-). This means that a solution of ammonia gas in water will be alkaline (basic), with a pH greater than 7.
Your problem states that you have a 0.6M solution of ammonia in water. If **all** the ammonia were converted to ammonium, then the solution would be easy, because [OH-] would equal [NH3], and then you'd calculate pOH, subtract it from 14, and voila.
But ammonia is a weak acid, so it doesn't completely dissociate, and we have a more challenging task.
For this reaction, we need to use the following:
Kb = Kw/Ka = [OH-]*[NH4+]/[NH3]
where Kb = base dissociation constant (NH3)
Kw = dissociation constant of water = 10E-14
Ka = dissociation constant of the conjugate acid (NH4+) = 5.62E-10
Kb = 1E-14/(5.62E-10) = 1.78E-05
Kb = 1.78E-05 = [OH-]*[NH4+]/[NH3]
We know the starting concentration of NH3 is 0.6M, but only some of that has dissociated into NH4+, so the ending concentration is 0.6-x. And since the dissociation of one molecule of ammonia produces one each of ammonium ion and hydroxide ion, [OH-] = [NH4+] = x, so:
1.78E-05 = (x^2)/(0.6-x)
converting this into quadratic form:
0 = x^2 + 1.78E-05x - 1.07E-05
and I will leave it to you to do the arithmetic of the quadratic equation to solve for x.
Once you have x, which is equal to [OH-], you can calculate pH by:
10E-14 = [H+]*[OH-], or
[H+] = 10E-14/[OH-], and
pH = -log[H+]
2006-09-06 10:56:14
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answer #2
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answered by Dave_Stark 7
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