A 0.10 M NH3 solution has a degree of dissociation 1.3% at temperature T. Calculate Kb for NH3 at this temperature?

Answer 1

#K_b = 1.7 * 10^(-5)#

To tackle this problem, two things are necessary for you to understand.

As you know, ammonia, #"NH"_3#, is a weak base, which means that it does not dissociate completely in aqueous solution to form ammonium ions, #"NH"_4^(+)#, its conjugate acid, and hydroxide anions, #"OH"^(-)#.
Instead, only a fraction of the number of molecules of ammonia will actually dissociate. That fraction depends on ammonia's base dissociation constant , #K_b#.
You are told that your ammonia solution has a degree of dissociation of #1.3%# at a given temperature #T#. What that means is that for every #100# molecules of ammonia present in solution, only #1.3# will dissociate.
Alternatively, you can think about it like this - for every #1000# molecules of ammonia, only #13# will ionize to form the aforementioned ions. The rest will remain as molecules of ammonia.

This is how the balanced chemical equation for this reaction appears.

#"NH"_text(3(aq]) + "H"_2"O"_text((l]) rightleftharpoons "NH"_text(4(aq])^(+) + "OH"_text((aq])^(-)#

The base dissociation constant by definition will be equal to

#K_b = (["NH"_4^(+)] * ["OH"^(-)])/(["NH"_3])#

You are aware of that

#["NH"_3] = "0.10 M"#
Now, use the degree of dissociation to find the concentrations of the two ions. You have #1:1# mole ratios between all chemical species, so you can say that
#["NH"_4^(+)] = ["OH"^(-)] = 1.3/100 * ["NH"_3]#
#["NH"_4^(+)] = ["OH"^(-)] = 1.3 * 10^(-2) * "0.10 M" = 1.3 * 10^(-3)"M"#

This implies that you receive

#K_b = (1.3 * 10^(-3) * 1.3 * 10^(-3))/0.10 = color(green)(1.7 * 10^(-5))#

The number of sig figs you have for the initial ammonia concentration is the answer, which is rounded to two sig figs.

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Answer 2

[K_b = \dfrac{[\text{NH}_4^+][\text{OH}^-]}{[\text{NH}_3]}]

Given that NH₃ dissociates as follows:

[ \text{NH}_3 + \text{H}_2\text{O} \rightleftharpoons \text{NH}_4^+ + \text{OH}^- ]

The degree of dissociation ((\alpha)) is given as 1.3%, which means (\alpha = 0.013).

Since NH₃ is a weak base, the concentration of NH₃ after dissociation is approximately equal to its initial concentration minus the concentration of NH₄⁺ formed. Therefore, ([NH_3] \approx [NH_3]_0 - [\text{NH}_4^+]).

Using the equilibrium expression:

[K_b = \dfrac{(x)(x)}{(0.10 - x)}]

Given that (\alpha = \frac{x}{0.10}), we can express (x) in terms of (\alpha).

Solving for (x):

[x = \sqrt{K_b(0.10 - x)}]

[x = \sqrt{K_b(0.10 - \alpha \times 0.10)}]

[x = \sqrt{K_b(0.10 - 0.013 \times 0.10)}]

[x = \sqrt{K_b(0.10 - 0.0013)}]

[x ≈ \sqrt{K_b \times 0.0987}]

[x ≈ 0.3137 \sqrt{K_b}]

Now, substituting the expression for (x) into the equation for (\alpha):

[0.013 = \frac{0.3137 \sqrt{K_b}}{0.10}]

[K_b ≈ \frac{(0.013 \times 0.10)^2}{0.3137^2}]

[K_b ≈ \frac{(0.0013 \times 0.10)^2}{0.3137^2}]

[K_b ≈ \frac{0.000169}{0.098187}]

[K_b ≈ 1.72 \times 10^{-3}]

So, (K_b) for NH₃ at this temperature is approximately (1.72 \times 10^{-3}) M.

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Answer from HIX Tutor

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

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