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Acid-Base & Equilibrium

pH, buffers, Ka/Kb, Le Chatelier, and solubility equilibria

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Acid-Base Chemistry and Equilibrium

pH, Strong and Weak Acids

Water autoionizes with Kw=[H+][OH−]=10−14K_w = [H^+][OH^-] = 10^{-14} at 25 degrees Celsius, so pH+pOH=14pH + pOH = 14 and pH=−log⁡[H+]pH = -\log[H^+] The seven strong acids and strong bases dissociate completely; weak acids only partially, with strength set by KaK_a (larger KaK_a, smaller pKapK_a, stronger acid). For a weak acid, approximate [H+]≈KaC[H^+] \approx \sqrt{K_aC}.

Buffers and Henderson-Hasselbalch

A buffer pairs a weak acid with its conjugate base and resists pH change: pH=pKa+log⁡[A−][HA]pH = pK_a + \log\frac{[A^-]}{[HA]} Buffering is best within one unit of pKapK_a. The bicarbonate system (CO2/HCO3−CO_2/HCO_3^-) stabilizes blood at pH 7.4, linking ventilation to acid-base status.

Titrations and Equilibrium

Weak acid-strong base titrations show a buffer region, half-equivalence where pH=pKapH = pK_a, and a basic equivalence point. For general equilibria, QQ vs. KK predicts reaction direction, Le Chatelier's principle predicts shifts from added species, pressure, or temperature, and KspK_{sp} governs solubility, which drops with a common ion.

Key Takeaways

  • Each pH unit is a tenfold change in [H+][H^+].
  • At half-equivalence, pH=pKapH = pK_a; at equivalence for a weak acid, pH is above 7.
  • Only temperature changes the value of KK; everything else shifts position only.
  • Conjugates: Ka×Kb=KwK_a \times K_b = K_w.
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pH, buffers, Ka/Kb, Le Chatelier, and solubility equilibria
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