Reactions of alkenes and alcohols

Cards (8)

  • Structure and formulae of alkenes:
    • Alkenes have the general formula CnH2n
    • They have at least one carbon-carbon double bond, making them unsaturated because they contain two fewer hydrogen atoms than the alkane with the same number of carbon atoms
    • The first 4 alkenes are ethene, propene, butene, and pentene
  • Reactions of alkenes:
    • Alkenes have the functional group C=C
    • They react with oxygen in combustion reactions, burning in air with smoky flames due to incomplete combustion
    • Alkenes react with hydrogen, water, and halogens by adding atoms across the carbon-carbon double bond to form a single bond
    • In each reaction with hydrogen, water, and halogens, the C=C bond is broken to form a C-C bond
    • The compound added splits into two groups added to the different carbons in the C=C bond
  • Alcohols:
    • Alcohols contain the functional group -OH
    • The first 4 members of the series are methanol, ethanol, propanol, and butanol
  • Reactions of methanol, ethanol, propanol, and butanol:
    • Alcohols burn in air, producing carbon dioxide and water
    • They dissolve in water to form a neutral solution with a pH of 7
    • Alcohols react with sodium to produce hydrogen and a salt
    • Alcohols react with oxidising agents to form carboxylic acids
  • Uses of methanol, ethanol, propanol, and butanol:
    • Methanol is used as a chemical feedstock, in anti-freeze, and to make biodiesel
    • Ethanol is the main alcohol in alcoholic drinks, used as a solvent and fuel
    • All 4 alcohols can be used as fuels
  • Producing ethanol:
    • Ethanol can be produced by fermentation of sugar with yeast using renewable sources
    • Conditions for fermentation: about 35°C, anaerobic, and yeast enzyme catalyst
    • Sugarethanol + carbon dioxide
  • Carboxylic acids:
    • Ethanoic acid is a member of the carboxylic acids, having the functional group -COOH
    • The first four members are methanoic acid, ethanoic acid, propanoic acid, and butanoic acid
  • Reactions of methanoic acid, ethanoic acid, propanoic acid, and butanoic acid:
    • They dissolve in water to produce acidic solutions with a pH less than 7
    • They react with metal carbonates to produce carbon dioxide, a salt, and water
    • React with alcohols in the presence of an acid catalyst to produce esters
    • Carboxylic acids do not ionise completely in solutions, making them weak acids with a higher pH than solutions of strong acids of the same concentration