MJ

Chapter 7 - Families of Organic Compounds

What Useful Compounds Does Crude Oil Contain?

Introduction to Hydrocarbons

  • Organic Chemistry: Deals with most compounds containing carbon.

  • Hydrocarbons: Compounds consisting of carbon and hydrogen only.

  • Examples of Organic Compounds:

    • Alkanes: e.g., ethane (CH3CH3)

    • Alkenes: e.g., ethene (CH2CH2)

    • Haloalkanes: e.g., chloroethane (CH3CH2Cl)

    • Alcohols: e.g., ethanol (CH3CH2OH)

    • Carboxylic Acids: e.g., ethanoic acid (CH_3COOH)

  • Misconceptions:

    • Carbon dioxide and carbonates are not considered hydrocarbons or organic compounds.

    • The term 'organic' in chemistry can refer to both natural and synthetic compounds.

Hydrocarbons

  • Hydrocarbon Definition: Compound consisting of carbon and hydrogen only.

  • Alkane Definition: Hydrocarbon containing only single carbon-to-carbon bonds.

    • General formula: CnH{2n+2}

  • Alkene Definition: Hydrocarbon containing at least one double carbon-to-carbon bond (C=C).

    • General formula: CnH{2n}

Homologous Series

  • Homologous Series Definition: Series of hydrocarbons with similar chemical structure and properties.

  • Alkanes Homologous Series: Differ by CH_2.

    • Methane (CH_4)

    • Ethane (C2H6)

    • Propane (C3H8)

    • Butane (C4H{10}

    • Pentane (C5H{12}

    • Hexane (C6H{14}

    • Heptane (C7H{16}

    • Octane (C8H{18}
      *Note: Spelling of chemical names is important.

Homologous Series - Alkenes

  • Alkenes homologous series: contains at least one C = C double bond.

    • Ethene (C2H4)

    • Propene (C3H6)

    • Butene (C4H8)

    • Pentene (C5H{10}

    • Hexene (C6H{12}

    • Heptene (C7H{14}

    • Octene (C8H{16}

Hydrocarbon Bonding

  • Intramolecular Bonding: Covalent within hydrocarbon molecules.

  • Carbon Chain: Linear set of carbon atoms.

  • Intermolecular Forces (IMF): Dispersion forces are the strongest IMF in alkenes and alkanes due to their non-polar nature.

Saturated vs Unsaturated Hydrocarbons

  • Saturated Hydrocarbons (Alkanes): Contain only single bonds between carbon atoms.

  • Unsaturated Hydrocarbons (Alkenes): Contain at least one carbon-to-carbon double bond.

Boiling Point of Alkanes

  • Physical Properties: Boiling point, melting point, and viscosity are influenced by intermolecular forces (IMF).

  • Boiling Point Trend: Increases with the number of carbons due to increased dispersion forces.

    Number of Carbons

    Boiling Point (ยฐC)

    State at 25ยฐC

    1

    -164

    gas

    2

    -89

    gas

    3

    -42

    gas

    4

    -1

    gas

    5

    36

    liquid

    6

    69

    liquid

    7

    98

    liquid

    8

    125

    liquid

Chemical Reactivity of Alkanes and Alkenes

  • Alkenes: More reactive than alkanes due to the presence of a C=C double bond (electron-rich).

    • Type of reactions: Addition, incomplete combustion

    • Enables other atoms to be added to C.

  • Alkanes:

    • Type of reactions: Substitution (in presence of UV light), combustion.

    • Less reactive.

    • Application: Fuels, starting material for synthesis of other chemicals.

  • Substitution Reaction: One atom or group of atoms replaces part of another molecule.

  • Addition Reaction: One molecule combines with another to form a larger molecule.

Summary

  • Hydrocarbons: Contain carbon and hydrogen.

  • Alkanes: Saturated hydrocarbons with single bonds between carbons.

    • General formula: CnH{2n+2}

  • Alkenes: Unsaturated hydrocarbons with at least one C=C double bond.

    • General formula: CnH{2n}

  • Homologous Series: Family of compounds that differ by CH_2.

  • Intermolecular Forces: Dispersion forces between adjacent molecules.

  • Boiling Point: Increases with carbon chain length due to stronger dispersion forces.

  • Chemical Properties:

    • Alkanes are less reactive than alkenes.

      • Undergo combustion and substitution reactions.

    • Alkenes undergo incomplete combustion and addition reactions.

Nomenclature (Part 1)

  • Nomenclature: System developed by the International Union of Pure and Applied Chemistry (IUPAC) to name organic compounds.

  • Systematic Name: Standardized name used to identify organic compounds.

  • Examples:

    • CH2O2: formic acid (common name), methanoic acid (systematic name)

    • C2H4O_2: acetic acid (common name), ethanoic acid (systematic name)

    • C4H8O_2: butyric acid (common name), butanoic acid (systematic name)

    • C3H6O: acetone (common name), propanone (systematic name)