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Alkanes Simplified Revision Notes

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Alkanes

Alkanes are saturated hydrocarbons that exhibit single covalent bonds between carbon atoms. This structural characteristic imparts high stability, making alkanes a fundamental topic in organic chemistry.

Key Definitions

  • Alkane: Saturated hydrocarbons distinguished by the presence of single covalent bonds.

    infoNote
    • Alkane: Hydrocarbons characterised solely by single carbon-carbon bonds.
  • Saturated Hydrocarbons:

    • Hydrocarbons composed exclusively of single bonds, maximising hydrogen atom content per carbon atom.

Introduction to Alkanes

  • Alkanes follow the general formula CnH2n+2C_nH_{2n+2}.
  • They play a vital role in fuel production, offering significant energy release upon combustion.
  • Alkanes are essential building blocks in organic chemistry, with properties varying based on chain length and branching.

Physical Characteristics

  • Alkanes are colourless and odourless.
  • Small alkanes (e.g., methane, ethane) are gases, medium-sized alkanes (e.g., hexane, heptane) are liquids, while larger alkanes (e.g., decane) are solids.

Molecular diagram showing a simple linear alkane structure to illustrate saturation and single bonds.

Table indicating the state (gas, liquid, solid) of different alkanes at room temperature.

Role in Fuel Production

  • Common reaction: Alkane+O2CO2+H2O+energy\text{Alkane} + \text{O}_2 \rightarrow \text{CO}_2 + \text{H}_2\text{O} + \text{energy}
  • Fuels such as petrol and diesel are derived from alkanes.
chatImportant

Alkanes are crucial to the energy industry due to their high heat output.

Simple chemical reaction diagram demonstrating combustion of an alkane for energy release.

Industrial Importance

  • Alkanes are modified to produce compounds like ethylene.
  • Catalytic techniques enhance combustion productivity, although they release carbon dioxide, leading to efforts to reduce environmental impact.
chatImportant

Comprehending the role of alkanes is vital for organic chemistry principles and industrial applications.

Bonding in Alkanes

  • Alkanes contain only single bonds, rendering them saturated and stable.
  • Sigma bonds (σ) are formed through sp³ hybridisation, contributing to the structure's stability and resulting in a tetrahedral geometry.

Diagram showing sigma bonds between carbon atoms and between carbon and hydrogen atoms demonstrating sp³ hybridization.

  • Intramolecular and Intermolecular Forces:
    • Intramolecular bonds maintain molecular structure.
    • Weak intermolecular van der Waals forces influence physical properties such as boiling points.

Physical Properties

  • Molecular size affects boiling/melting points; larger molecules possess higher points due to increased van der Waals forces.
  • Branching decreases boiling/melting points.

Diagrams comparing molecular interactions in linear and branched alkanes.

Volatility and Density

  • Volatility decreases as molecular mass increases.
  • Density generally rises with chain length due to more compact molecular packing.

Graph showing differences in volatility across the homologous series of alkanes.

Functional Groups in Alkanes

  • Alkanes Lack Functional Groups:
    • Their simple structures contribute to stability.
    • They primarily undergo combustion and substitution reactions.
chatImportant

Stability ensures predictable reactions but limits chemical versatility.

Formulae

  • Structural Formula:
    • Demonstrates atom arrangement.
  • Molecular Formula:
    • Lists atom quantities.
  • Formulating involves determining the root name and employing CnH2n+2C_nH_{2n+2} to represent hydrogen content.

Annotated diagrams of structural and molecular formulae for each alkane from methane to octane.

Model Construction

  • Models visually depict three-dimensional atomic interactions.
  • Ball-and-stick models, though potentially misrepresenting bond angles, facilitate comprehension.

Illustrates the tetrahedral structure due to sp³ hybridization.

Practice Problems and Solutions:

Problem 1: Identify and Draw

Task: Illustrate pentane's structural and molecular formulas.

Solution:

  • Molecular formula: C₅H₁₂
  • Structural formula: CH₃-CH₂-CH₂-CH₂-CH₃
  • Ensure all carbon atoms have four bonds each to satisfy valency

Problem 2: Boiling Points

Task: Compare the boiling points of butane and 2-methylpropane.

Solution:

  • Butane (linear structure) has a higher boiling point than 2-methylpropane (branched structure)
  • This is because the linear structure allows for stronger van der Waals forces between molecules, requiring more energy to separate

Diagram depicting structures of butane and 2-methylpropane to highlight boiling point differences.

Problem 3: Combustion Reaction

Task: Formulate the balanced combustion equation for hexane.

Solution:

  • Unbalanced: C₆H₁₄ + O₂ → CO₂ + H₂O
  • Balanced: C₆H₁₄ + 9½O₂ → 6CO₂ + 7H₂O
  • Alternatively: 2C₆H₁₄ + 19O₂ → 12CO₂ + 14H₂O (with whole numbers)

Balanced chemical equation diagram for hexane combustion.

Problem 4: Combustion Types in Octane

Task: Differentiate between complete and incomplete combustion.

Solution:

  • Complete combustion: C₈H₁₈ + 12½O₂ → 8CO₂ + 9H₂O
    • Occurs with excess oxygen
    • Produces carbon dioxide and water only
  • Incomplete combustion: C₈H₁₈ + limited O₂ → mixture of CO₂, CO, C (soot), H₂O
    • Occurs with insufficient oxygen
    • Produces carbon monoxide, carbon (soot), and/or unburnt fuel in addition to CO₂ and H₂O

Comparison diagrams of complete vs. incomplete combustion of octane.

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