Ka greater than one=strong acid?

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Ka for strong acids is irrelevant but yes that seems too low for strong acids as 1 means half-dissociating in water
 
Ka for strong acids is irrelevant but yes that seems too low for strong acids as 1 means half-dissociating in water

Why Ka is irrelevant? I thought that the strong acid by definition is the acid that disassosiates completely. (is that correct?) Well, nothing is complete, and that means that Ka is just a very very big number, like 10^60 , it may not be measurable since [HA] concentration is very small. Ka=1 does not look like a big number to me 🙂
 
Why Ka is irrelevant? I thought that the strong acid by definition is the acid that disassosiates completely. (is that correct?) Well, nothing is complete, and that means that Ka is just a very very big number, like 10^60 , it may not be measurable since [HA] concentration is very small. Ka=1 does not look like a big number to me 🙂

your definition is correct.. i say it's irrelevant because it's so huge and serves no real purpose.
 
Yup, as an acid becomes stronger, it's Ka value approaches infinity (since the numerator is getting larger while the denominator is getting closer to zero). A Ka > 1 means that the acid is strong since it dissociates a significant amount compared to weak acids (10^-14 < Ka < 1). A Ka of 1 means that more than half of HA has dissociated (since x2 is in the numerator).
 
no a Ka of 1 would be exactly half - hardly acceptable under the casual "strong acid" definition
Hmm...isn't the equation Ka =[H+][A-]/[HA]? And at equilibrium (for example initial [HA] = 1M), [H+] = [A-] = x, while [HA] = 1 - x? So, 1 = (x^2)/(1-x). If half of it has dissociated, wouldn't the value of x be 0.5, so (0.5*0.5)/(0.5) equals 0.5, not 1?

Chemistry is not my greatest strength, but that's what I remember from my review. Am I missing something?
 
i did:

2M HA --> 1M HA + 1M A- + 1M H+

[1][1]/[1] = 1

hmm... but your math is correct as well... hmmmmmmm
 
both of us might be doing this completely wrong... i.e. changing the original concentration actually changes the ratio of [a-]:[ha] because the K value is a ratio of [a-]^2:[ha]

ah i learned somethign today... nice.
 
What is the problem?
for HA -> H + A
x^2/(1-x) = 1 => x^2=1-x => x^2+x-1=0
x = (-1 +/- Sqrt(1+4))/2 = (-1 +/- Sqrt(5))/2
Minus doesn't works since x become <0 so
x=(-1+Sqrt(5))/2 ~ 0.6.
We have HA left 0.4
H and A produced ~ 0.6
Not exactly half but close enough.
 
given a fixed Ka, the ratio of [a] to [ha] shifts depending on originial [ha]. which makes sense. i.e. an acid that might dissociate exactly halfway at a certain concentration will not at another.l
 
given a fixed Ka, the ratio of [a] to [ha] shifts depending on originial [ha]. which makes sense. i.e. an acid that might dissociate exactly halfway at a certain concentration will not at another.l

Agree,
Skipping the math it looks like When [HA]=2 the dissociation will be exactly halfway
 
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