Ka is defined as the ratio [H+][R-]/[HR]
where HR is the un-ionized form of the acid and R is the ionized form, and [X] stands for "concentration of X"
Also, since the total solution has no net charge, [H+] = [R-] (the positive and negative ions have equal concentrations)
Finally, the total concentration of the acid is [R-] + [HR], which in this case is given as 2 moles. You can then write
[R-] = 2 -[RH].
Combining these equations with the known value for Ka you get:
1.29 x 10^-4 = [H+][H+]/(2 - [H+])
This gives the quadratic [H+]^2 + Ka[H+] - 2Ka = 0.
However, a useful shortcut is to recognize that [H+] is usually very small - remember that pH = -log[H+]. So [H+] << 2 and we can write:
1.29 x 10^-4 = [H+][H+]/(2)
or in general terms Ka = [H+]^2/Ctotal
Then we solve for [H+] = sqrt(2*1.29 x 10^-4) = 0.0161
and pH = -log10([H+]) = - log10(.0161) = 1.79 or in round numbers, pH = 1.8.
2006-09-01 14:34:57
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answer #1
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answered by Samienela 3
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Ka = [H+][base anion]/[unionized acid]
First lets get a rough idea by assuming that the total amount ionized is so small that it does not effect the concentration of the uric acid, so we keep uric acid concentration at 2 M, this way we avoid using quadratic equations.
1.29 x 10^-4 = [H+][base anion]/[2 Molar], note that the concentration of the h+ and the base anion are the same so we can rewrite as follows:
1.29x10^-4 = [H+]^2/[2M]
Solve for [H+] = sqrt(2*1.29*10^-4) = 0.016 molar
Is 0.016 enough to really change the calculated value of Ka to justify the messy quadratic equation, lets check
(0.016)(0.016)/[2-0.016] = ?
? = 1.29x10^-5, which is the true value of the Ka.
So, we can go with this approach and [h+] = 0.016 molar
If the calculated value of Ka was off very much we would resort to the quadratic equation below.
1.29*10^-4 = [x]^2/(2-x) which implies
x^2 - (2-x)*1.29*10^-4 = 0, solve for x
x^2 +(1.29*10^-4)x - 2.58*10^-4 = 0
x = 0.016, now lets check this answer for errors
Ka = ? = (1.6*10^-2)^2/[2 - 1.6*10^-2] = 1.29 * 10^-4
Looks like it is close enough to the actual Ka value.
So, the [H+] is 1.6*10^-2
ph then is -log[1.6*10-2] = 1.79
please check for errors.
2006-09-01 16:37:04
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answer #2
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answered by Anonymous
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This is a little tricky, but not impossible. The Ka=[H][urate]/[uric acid], and remeber that for as much uric acid dissiocates you get just as much Hydronium and urate. So just set up an algebra equation (make the ammount made/lost "x").
1.29*10^-4 = x^2 / 2-x ; now, we can assume that 2>>x, making the equation
1.29*10^-4 = x^2/2 (multiply the 2 on both sides)
2.58*10^-4 = x^2 (find the square root of both sides)
x = 0.016062 (keep two extra digits to avoid rounding errors, 5sf)
Check your assumption (that 2 is way bigger than x) 2/0.016062=124.5, the assumption is good enough for general chem
Now, the H+ concentration = 0.016062 so take the negative log of that number to get pH.
pH=1.79
2006-09-01 14:31:00
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answer #3
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answered by Jonathan M 2
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more than 0 but less than 7
2006-09-01 14:08:19
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answer #4
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answered by rob 1
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Acidic so more than 7.0 pH
2006-09-01 14:08:55
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answer #5
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answered by rav 4
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is a acid base solution
2006-09-01 14:11:42
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answer #6
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answered by icac83 3
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