High School Chemistry: Find pH of Solutions A and C | Acid-Base Equilibrium

AI Thread Summary
To find the pH of Solution A, which is a 0.100 M weak monoprotic acid HX, the equilibrium constant expression is used, leading to the calculation of [H+] as approximately 0.0268 M. For Solution C, created by adding KOH to Solution A, it is important to determine whether there is an excess of HX or KOH, as this influences whether the solution acts as a buffer. The calculations for pH in Solution C depend on the relative concentrations of HX and KX, with the need to consider both Ka and Kb values. The discussion emphasizes that a buffer requires the presence of both the weak acid and its conjugate base simultaneously. Understanding these relationships is crucial for accurately calculating pH in acid-base equilibrium scenarios.
jacker2011
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Homework Statement


Find pH of solution A and that of Solution C with the following information below:

Solution A:50ml of 0.100 M solution of weak monoprotic acid HX
Solution B: 0.0500M solution of salt NaX. It has a pH of 10.02
Solution C: made by adding 15.0m; of 0.250 M KOH to solution A


Homework Equations


Ka for monoprotic acid is 7.2 x 10^-4, Ka=[H+] [anion]. Anion= x
1/2log(Ka)=[H+]


The Attempt at a Solution



i try to find [H+] which i did was 1/2log(Ka)=
1/2log (7.2 x 10^-4) = 0.0268
or I find the M of [H+] in solution A
and i found 0.005M of HX
 
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The simplification not being immediately obvious to me, I find that the equilibrium constant expression for the weak acid could generally be:
\[<br /> K_a = \frac{{[H][H]}}{{F_a - [H]}}<br /> \]
Which is easily transformed to \[<br /> [H]^2 + K_a [H] - K_a F = 0<br /> \]
You can from there use the solution to a quadratic equation. In that equation, \[F_a \] is formality of the acid, and [H] is molarity of hydrogen ion (or hydronium).

For solution #c, note if you have excess HX or excess KOH. If you have excess HX, then you have a solution containing HX and KX, meaning this is a buffer. Base your calculations on the modification required for the Ka formula (my best guess, right now - depends on relative ratios and strength of Ka and Kb; the KX has a Kb value while the HX has a Ka value.)
 
What jacker2011 aims at is [H+]=sqrt(Ka*C), which works for dissociation degree smaller than 5% (see discussion of calculation of pH of weak acid for details).

Buffer solution is not about containing HX and KX, but about containing HX and X- at the same time (ie acid and conjugated base). That's close, but it is not the same.
 
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