If the #"pH"# of an aqueous solution of ammonium chloride is #4.60#, what is the #K_h# value of #"NH"_4^(+)#?

Answer 1
I assume it's an error in your notes? The relationship between #K_a#, #K_b#, and #K_w# is that #K_a*K_b = K_w = 10^(-14)#.
Even though you are not given #K_a#, you can still look it up. I happen to remember the #K_b# for #"NH"_3# though, so here's an opportunity to demonstrate the relationship.
The #K_b# for ammonia, #"NH"_3#, is related to the #K_a# for ammonium, #"NH"_4^(+)#.
#K_b = 1.8 xx 10^(-5)#
#K_w = 10^(-14)#

Consequently:

#K_a = K_w/K_b = 10^(-14)/(1.8 xx 10^(-5)) = 5.55 xx 10^(-10)#
So, the #K_a# for #"NH"_4^(+)# is #5.55 xx 10^(-10)#, and this is what you would expect for your answer.. You should also be able to look this up in the Appendix of your textbook.

Presume for a moment that you were unaware of that. After building your ICE table:

#"NH"_4^(+)(aq) + "H"_2"O"(l) rightleftharpoons "NH"_3(aq) + "H"_3"O"^(+)(aq)#

You ought to obtain:

#K_a = (x^2)/(0.1 - x) = ?#
If you aren't sure how I got here, tell me. #"NH"_4^(+)# is a weak acid since #"NH"_3# is a weak base. When you look at the #K_b# for a weak base, it is moderately small. Therefore, for the conjugate weak acid, it is even smaller.
When we calculate #K_a#, do NOT use the small #x# approximation, because it will not work unless #K_a# is small enough. Beyond that, you should only use it when you use #K_a# in the first place.
We know #"pH" = 4.60 = -log["H"^(+)]#. So:
#["H"^(+)] = x = 10^(-4.60)#

Consequently:

#color(blue)(K_a) ~~ (10^(-4.60))^2/(0.1 - 10^(-4.60)) = color(blue)(6.310 xx 10^(-9))#
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Answer 2

First calculate Ka then we can calculate Kh

I'm going to find the Ka from a different way you may dont know which is only applicable to weak acids

When we solve for Ka

we do this

#sqrt("Ka" xx "molarity") = m#
#-log(m) = pH#

so by solving for m when given the pH we can find the answer of square root.

so -log(x) = 4.60

x = #10^-4.60# x = 0.00003
#sqrt("Ka" xx " 0.1M") = 0.00002511886#

solve for Ka

#Ka xx 0.1 = 0.00002511886^2#
#6.30957344e-9 = Ka#
#K_h = K_w/ (Kb)# and u will again get the Ka

For acids like this Ka = Kh

Oswald's law of dillution can be used to calculate Ka of weak electrolytes or weak acids like this one

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Answer 3

The ( K_h ) value for ( NH_4^+ ) can be calculated using the formula:

[ K_h = 10^{-\text{pH}} ]

Plugging in the pH value of the ammonium chloride solution:

[ K_h = 10^{-4.60} ]

[ K_h \approx 2.51 \times 10^{-5} ]

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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.

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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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