Acids and bases

Here is an explanation of the core concepts covered in your notes:

1. Fundamental Theories of Acids and Bases
  • Arrhenius Theory: Focuses on aqueous solutions. An acid increases H+<em>(aq)H^+<em>{(aq)} concentration, while a base increases OH−</em>(aq)OH^-</em>{(aq)} concentration. Its limitation is that it only applies to water solutions and fails to explain substances like NH3NH_3 that act as bases without containing hydroxide ions.

  • Brønsted-Lowry Theory: Expands acid-base reactions to proton transfer. An acid is a proton (H+H^+) donor, and a base is a proton acceptor. When an acid loses a proton, it forms its conjugate base; when a base gains a proton, it forms its conjugate acid. Substances that can either donate or accept a proton (such as H<em>2OH<em>2O and HCO</em>3−HCO</em>3^-) are called amphiprotic.

  • Lewis Theory: Focuses on electron pairs. A Lewis acid accepts an electron pair into an empty orbital (e.g., BF<em>3BF<em>3), while a Lewis base donates a lone pair (e.g., NH</em>3NH</em>3). Their reaction forms a coordinate covalent bond.

2. Autoionization of Water and the pH Scale
  • Water naturally self-ionizes in an endothermic reaction: 2H<em>2O</em>(l)<br>ightleftharpoonsH<em>3O+</em>(aq)+OH(aq)−2H<em>2O</em>{(l)} <br>ightleftharpoons H<em>3O^+</em>{(aq)} + OH^-_{(aq)}.

  • The ion product constant of water at 298 K298\,K is K<em>w=[H+][OH−]=1.00×10−14 mol2 dm−6K<em>w = [H^+][OH^-] = 1.00 \times 10^{-14}\,mol^2\,dm^{-6}. Because the process is endothermic, increasing the temperature increases K</em>wK</em>w, shifting the neutral pHpH below 77.

  • The pHpH and pOHpOH scales quantify acidity and basicity logarithmically: pH=−log⁡<em>10([H+])pH = -\log<em>{10}([H^+]) and pOH=−log⁡</em>10([OH−])pOH = -\log</em>{10}([OH^-]). At 298 K298\,K, they relate by pH+pOH=14.00pH + pOH = 14.00.

3. Strong vs. Weak Acids and Bases
  • Strong Acids and Bases: Completely dissociate in water (α≈100%\alpha \approx 100\%), meaning [H+][H^+] or [OH−][OH^-] is directly determined from the initial concentration.

  • Weak Acids and Bases: Only partially dissociate and reach dynamic equilibrium. Their strengths are measured by dissociation constants (K<em>aK<em>a and K</em>bK</em>b) and their logarithmic values (pK<em>apK<em>a and pK</em>bpK</em>b). Lower values of pK<em>apK<em>a or pK</em>bpK</em>b signify stronger acids or bases. For a conjugate pair, K<em>a×K</em>b=K<em>wK<em>a \times K</em>b = K<em>w and pK</em>a+pKb=14.00pK</em>a + pK_b = 14.00 at 298 K298\,K.

4. Neutralization Reactions and Titrations
  • When acids and bases neutralize each other, the equivalence point pHpH depends on their relative strengths:

    • Strong acid + strong base yields a neutral solution (pH=7.00pH = 7.00 at 298 K298\,K).

    • Weak acid + strong base results in an equivalence point with pH>7pH > 7 due to conjugate base hydrolysis.

    • Strong acid + weak base results in an equivalence point with pH<7pH < 7 due to conjugate acid hydrolysis.

5. Buffer Solutions
  • Buffers resist changes in pHpH when small amounts of acid or base are added. An acidic buffer consists of a weak acid and its conjugate base salt (such as CH<em>3COOHCH<em>3COOH and $$CH3