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

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SUMMARY

This discussion focuses on calculating the pH of solutions A and C involving a weak monoprotic acid HX and a strong base KOH. Solution A consists of 50 mL of 0.100 M HX, while Solution C is created by adding 15.0 mL of 0.250 M KOH to Solution A. The dissociation constant (Ka) for the acid is 7.2 x 10^-4, and the equilibrium expression for the weak acid is derived using the quadratic formula. The discussion emphasizes the importance of recognizing buffer solutions and the relationship between Ka and Kb in determining pH.

PREREQUISITES
  • Understanding of weak acid dissociation and equilibrium constants (Ka)
  • Familiarity with pH calculations and logarithmic functions
  • Knowledge of buffer solutions and their components
  • Ability to solve quadratic equations in chemistry contexts
NEXT STEPS
  • Study the Henderson-Hasselbalch equation for buffer solutions
  • Learn about the relationship between Ka and Kb for conjugate acid-base pairs
  • Explore pH calculations for strong acid-strong base titrations
  • Investigate the effects of dilution on pH in weak acid solutions
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Chemistry students, educators, and anyone involved in acid-base equilibrium calculations will benefit from this discussion.

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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