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Acids and Bases: Properties, Definitions, and Strength (General Chemistry Study Notes)

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Acids and Bases: Properties, Definitions, and Strength

General Properties of Acids

Acids are a fundamental class of compounds in chemistry, characterized by their ability to donate protons (H+) and exhibit distinctive physical and chemical properties.

  • Sour taste: Many acids, such as citric acid in citrus fruits and acetic acid in vinegar, have a sour flavor.

  • Reaction with metals: Acids can dissolve many metals and metal oxides, often producing hydrogen gas.

  • Litmus test: Acids turn blue litmus paper red.

Examples of organic acids:

  • Acetic acid (CH3COOH): Found in vinegar.

  • Citric acid (C6H8O7): Present in citrus fruits.

  • Malic acid (C4H6O5): Found in apples and grapes.

Acetic acid in vinegar bottleCitric acid and malic acid in fruitsCitric acid and malic acid in fruits

Carboxylic acids: A common functional group in organic acids is the carboxylic acid group (-COOH).

Carboxylic acid group structure

  • Inorganic acids: Examples include hydrochloric acid (HCl), sulfuric acid (H2SO4), and nitric acid (HNO3).

Sulfuric acid and nitric acid structures

General Properties of Bases

Bases are substances that accept protons or donate electron pairs, and they have their own set of characteristic properties.

  • Bitter taste: Many bases taste bitter, which may be an evolutionary adaptation to avoid toxic alkaloids.

  • Slippery feel: Bases react with oils on the skin to form soap-like substances, giving a slippery sensation.

  • Litmus test: Bases turn red litmus paper blue.

Household cleansers containing bases

Examples of inorganic bases:

  • Sodium hydroxide (NaOH)

  • Sodium bicarbonate (NaHCO3)

  • Ammonia (NH3)

  • Sodium carbonate (Na2CO3)

Alkaloids: Organic bases found in plants, some of which are toxic, while others like caffeine are not.

Caffeine structure and coffee beans

Definitions of Acids and Bases

Arrhenius Definition

The Arrhenius definition is the simplest and most restrictive, focusing on aqueous solutions:

  • Acid: Produces H+ ions in aqueous solution.

  • Base: Produces OH− ions in aqueous solution.

Arrhenius acid and base in solution

Limitations: Only applies to aqueous solutions and cannot explain all acid-base behavior, such as that of ammonia (NH3).

Brønsted–Lowry Definition

The Brønsted–Lowry theory broadens the concept to include proton transfer reactions:

  • Acid: Proton (H+) donor.

  • Base: Proton (H+) acceptor.

This definition applies to a wider range of reactions, including those in non-aqueous solutions.

Lewis Definition

The Lewis definition is the most general:

  • Acid: Electron pair acceptor.

  • Base: Electron pair donor.

This definition encompasses many reactions not covered by the other two definitions.

Strong and Weak Acids and Bases

Strong Acids

Strong acids completely ionize in water, meaning all acid molecules donate their protons to water.

  • Examples: HCl, HBr, HI, HNO3, H2SO4

Complete ionization of HCl in water

Weak Acids

Weak acids only partially ionize in water, so a significant amount of the acid remains un-ionized.

  • Examples: HF, acetic acid (HAc), many organic acids

Partial ionization of HF in water

Strong and Weak Bases

Strong bases, such as NaOH and KOH, completely dissociate in water to produce OH− ions. Weak bases, like ammonia (NH3), only partially react with water to produce OH−.

Complete ionization of NaOH in water

Brønsted–Lowry Acid–Base Reactions and Conjugate Pairs

Proton Transfer and Amphoterism

Brønsted–Lowry acid–base reactions involve the transfer of a proton from the acid to the base. Substances like water that can act as both an acid and a base are called amphoteric.

Conjugate Acid–Base Pairs

Each acid–base reaction involves two conjugate acid–base pairs. The acid becomes its conjugate base after donating a proton, and the base becomes its conjugate acid after accepting a proton.

Conjugate acid-base pairs: NH3/NH4+ and H2O/OH-

Acid Strength and Molecular Structure

Binary Acids (H–Y)

The strength of binary acids depends on bond polarity and bond strength:

  • Bond polarity: More polar H–Y bonds (with Y more electronegative) lead to stronger acids.

  • Bond strength: Weaker H–Y bonds are easier to break, resulting in stronger acids.

Acidity trends in binary acidsTable of binary acid strength and electronegativity

Oxyacids (H–O–Y)

The strength of oxyacids depends on:

  • Electronegativity of Y: Higher electronegativity increases acid strength.

  • Number of oxygen atoms: More oxygen atoms bonded to Y increase acid strength.

General structure of oxyacidTable of oxyacid strength and structureTable of acid strength for perchloric, chloric, and hypochlorous acids

Acid Ionization Constant (Ka)

The acid ionization constant, Ka, quantifies the extent to which a weak acid ionizes in water:

  • Large Ka: Indicates a stronger acid (more complete ionization).

  • Small Ka: Indicates a weaker acid (less ionization).

The general expression for a weak acid HA is:

For strong acids, the reaction goes to completion and Ka is not typically used.

Autoionization of Water and the pH Scale

Autoionization of Water

Water can react with itself to form hydronium and hydroxide ions:

The ion product constant for water at 25°C is:

The pH Scale

The pH scale is a logarithmic measure of the hydrogen ion concentration:

  • Acidic solution: pH < 7 ([H+] > 1.0 × 10−7 M)

  • Neutral solution: pH = 7 ([H+] = 1.0 × 10−7 M)

  • Basic solution: pH > 7 ([H+] < 1.0 × 10−7 M)

Significant figures in pH calculationsSignificant figures in pH calculationsThe pH scale diagram

An increase of 1 unit on the pH scale corresponds to a tenfold decrease in [H+].

Summary Table: Strong and Weak Acids

Name

Formula

Strong/Weak

Hydrochloric acid

HCl

Strong

Hydrobromic acid

HBr

Strong

Nitric acid

HNO3

Strong

Perchloric acid

HClO4

Strong

Sulfuric acid

H2SO4

Strong (diprotic)

Hydrofluoric acid

HF

Weak

Acetic acid

HC2H3O2

Weak

Formic acid

HCHO2

Weak

Sulfurous acid

H2SO3

Weak (diprotic)

Carbonic acid

H2CO3

Weak (diprotic)

Key Equations

  • (at 25°C)

TL;DR (Summary)

  • Brønsted–Lowry definition: Acids are proton donors, bases are proton acceptors.

  • Molecular structure: Determines acid strength (electronegativity, bond strength, number of oxygens).

  • Acid ionization constant (Ka): Larger Ka means a stronger acid.

  • Water autoionization: at 25°C.

  • pH scale: ; each unit change is a tenfold change in [H+].

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