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Acids and Bases: Definitions, Strength, Dissociation, and Amphoteric Water

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Chapter 10: Acids and Bases

10.1 Definitions

This section introduces the fundamental definitions of acids and bases, focusing on the hydronium ion and classical models.

  • Hydronium Ion (H3O+): The ion formed when an acid reacts with water. It is central to acid-base chemistry in aqueous solutions.

  • Arrhenius Definition:

    • Acid: A substance that produces hydronium ions (H3O+) when dissolved in water. Example Reaction:

    • Base: A substance that produces hydroxide ions (OH-) when dissolved in water. Examples:

      • Metal Hydroxides: Ionic compounds (e.g., NaOH) that release OH- directly.

      • Molecular Compounds: Substances like ammonia (NH3) that react with water to produce OH-.

  • Brønsted-Lowry Definition:

    • Acid: Proton donor (gives a hydrogen ion, H+, to another molecule or ion). Solvent Independent: The reaction does not need to occur in water. H+ Transfer: The defining characteristic is the transfer of a proton to a base.

    • Base: Proton acceptor (accepts H+ from an acid). Lone Pair Requirement: Must have a lone pair of electrons to bond with the incoming proton (e.g., NH3).

  • Polyprotic Acids: Acids that can donate more than one proton per molecule.

    • Monoprotic: HCl (1 proton)

    • Diprotic: H2SO4 (2 protons)

    • Triprotic: H3PO4 (3 protons)

  • Conjugate Acid-Base Pairs:

    • Pairs of chemical species found on opposite sides of a chemical reaction, differing by one hydrogen ion (H+).

    • General Reaction:

10.2 Acid and Base Strength

This section analyzes the strength of acids and bases and how it affects chemical equilibria.

  • Strong Acids:

    • Give up a proton easily; nearly 100% dissociated in water.

    • Reaction goes essentially to completion.

  • Weak Acids:

    • Give up a proton with difficulty; only partially dissociated.

    • Equilibrium favors the undissociated form.

  • Strong Bases:

    • Hold a proton tightly; high affinity for H+.

  • Weak Bases:

    • Have little affinity for a proton; do not hold H+ tightly.

  • Stepwise Dissociation:

    • Polyprotic acids lose protons in steps. Step 1: Nearly 100% extent for strong first-stage acids. Step 2: Much lesser extent due to electrostatic difficulty in removing a proton from a negatively charged ion.

  • Inverse Strength Relationship (Seesaw Rule):

    • Stronger Acid → Weaker Conjugate Base

    • Weaker Acid → Stronger Conjugate Base

  • Predicting Equilibrium:

    • Equilibrium favors the reaction of the stronger acid with the stronger base.

    • The reaction proceeds to form the weaker acid and the weaker base.

10.3 Acid Dissociation Constants (Ka)

This section explores the acid dissociation constant as a predictor of acid strength.

  • Expression for Ka:

  • Interpreting Ka Values:

    Type

    Ka Value

    Interpretation

    Strong Acid

    Ka >> 1

    Dissociation is highly favored.

    Weak Acid

    Ka << 1

    Dissociation is not favored.

    Organic Acids

    ~10-5

    Typically weak acids (contain –COOH).

10.4 Amphoteric Water

This section examines water's unique role acting as both an acid and a base.

  • Amphoteric Substance: Can react as either an acid or a base.

  • As a Base: Accepts a proton when in contact with an acid.

  • As an Acid: Donates a proton when in contact with a base.

Ion-Product Constant (Kw)

Water undergoes autoionization, forming hydronium and hydroxide ions in equal amounts.

  • Autoionization Reaction:

  • Value of Kw at 25°C:

Solution Classification

Solutions are classified based on the relative concentrations of hydronium and hydroxide ions.

Type

[H3O+]

[OH-]

Acidic

> 10-7

< 10-7

Neutral

= 10-7

= 10-7

Basic

< 10-7

> 10-7

Example:

If [H3O+] = 1.0 × 10-4 M and [OH-] = 1.0 × 10-10 M, the solution is acidic.

Additional info: These notes expand on the provided slides with definitions, equations, and examples for clarity and completeness.

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