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Overview of Alcohols and Their Reactions

Apr 16, 2025

Alcohols Overview - OCR-A Revision

Introduction to Alcohols

  • Alcohols have the functional group OH (hydroxyl group).
  • Alcohols belong to the homologous series: CₙH₂ₙ₊₁OH.
  • Types of alcohols:
    • Primary Alcohol: OH group attached to a carbon bonded to one other carbon (e.g., butan-1-ol).
    • Secondary Alcohol: OH group attached to a carbon bonded to two other carbons (e.g., butan-2-ol).
    • Tertiary Alcohol: OH group attached to a carbon bonded to three other carbons.

Solubility of Alcohols

  • OH bond in alcohols is polar; delta negative on oxygen.
  • Hydrogen bonding occurs between alcohols and water, aiding solubility.
  • Short-chain alcohols (e.g., methanol, ethanol) are more soluble due to less non-polar hydrocarbon chain.
  • Longer hydrocarbon chains result in decreased solubility.

Boiling Points and Volatility

  • Alcohols have higher boiling points than similar mass alkanes due to hydrogen bonding.
  • Less volatile than alkanes.

Formation of Haloalkanes

  • Haloalkanes formed via substitution reactions.
  • Alcohol reacts with halide ions and an acid catalyst (e.g., sodium bromide + sulfuric acid) to form haloalkane (e.g., 2-bromobutane).

Dehydration of Alcohols

  • Alcohols dehydrate to form alkenes by removing water.
  • Requires acid catalysts (e.g., sulfuric or phosphoric acid).
  • Useful for creating polymers and plastics.
  • Non-primary alcohols > 3 carbons can form different positional isomers and E/Z isomers.

Combustion of Alcohols

  • Alcohols burn with a light blue flame, forming CO₂ and H₂O.
  • Can be oxidized with potassium dichromate, forming aldehydes, ketones, or carboxylic acids.

Oxidation of Alcohols

  • Primary Alcohols can be oxidized:
    • To Aldehydes, then further to Carboxylic Acids.
    • Requires distillation to capture aldehyde before further oxidation.
    • Reflux used for full oxidation to carboxylic acids, allowing strong heating without loss.
  • Secondary Alcohols oxidized to Ketones only, using reflux.
  • Primary can't oxidize further with potassium dichromate.

Practical Techniques

  • Distillation: Used to isolate aldehydes by removing them as they form.
  • Reflux: Allows strong heating without losing volatile compounds, used for full oxidation to carboxylic acids.

Conclusion

  • Key reactions and properties of alcohols are covered, essential for OCR-A exams.
  • Further support and resources are available for deeper study.