2.7 - Alcohols and Carboxylic Acids

Cards (28)

  • What is the functional group of alcohols?
    Hydroxyl/ -OH group
  • What is the general formula for alcohols?
    Cn H2n+1 OH
  • What are the conditions for the industrial production of ethanol from ethene? (Hydration to go from alkene to alcohol)
    • Steam
    • Phosphoric acid (aq)
    • 300 degrees celsius
    • High pressure
  • How can ethanol be produced from a renewable source?
    Ethanol can be produced from the fermentation of sugars
  • How can alcohols be produced from alkenes?
    • Fermentation
    • Industrial hydration
  • What conditions are needed for the fermentation of sugars to form ethanol?
    • Yeast
    • 30-40 degrees celsius
    • Anaerobic conditions
  • Why is the production of ethanol from sugars said to be 'carbon neutral'?
    Ethanol when used as a fuel released carbon dioxide, which will be taken in by crops during photosynthesis. This balances out the carbon dioxide that is released when the ethanol is burned.
  • Why might someone arue that the production of ethanol from fermentation of sugars is no carbon-neutral?
    Energy is required to power the harvesting, transportation, etc. of the crops and ethanol. This energy will come from the burning of fuel, releasing carbon dioxide.
  • What is formed when alcohols undergo dehydration?
    Alkenes and a water molecule
  • What are the conditions for dehydrating an alcohol?
    Either
    • heat with a strong acid catalyst (sulfuric acid)
    • pass vapour over an aluminium oxide catalyst
  • How are alcohols classified?
    Alcohols are classified based on the number of carbon atoms bonded to the carbon atom that bears the hydroxyl group.
  • Primary alcohols...
    one R group is bonded to the carbon with a hydroxyl group on it
  • Secondary alcohols...
    two R groups are bonded to the carbon with a hydroxyl group on it
  • Tertiary alcohols...
    three R groups are bonded to the carbon with a hydroxyl group on it
  • What are primary alcohols oxidised to form?
    Aldehydes
  • How are primary alcohols oxidised to aldehydes?
    Heat the primary alcohol with acidified potassium dichromate and distill - when completed the potassium dichromate will turn from orange to green
  • How are primary alcohols oxidised to form carboxylic acids?
    Heat the primary alcohol under reflux with acidified potassium dichromate - when completed the potassium dichromate will turn from orange to green
  • What are secondary alcohols oxidised to form?
    Ketones
  • How are secondary alcohols oxidised to form ketones?
    If a secondary alcohol is heated under reflux with acidified potassium dichromate, it will form a ketone - when complete the acidified potassium dichromate will turn from orange to green
  • What qualitative test can be carried out for the identification of primary and secondary alcohols?
    Add acidified potassium dichromate - if either alcohol is present it will turn from orange to green
  • What test can be carried out to identify carboxylic acids?
    Add sodium hydrogencarbonate (NaHCO3) - fizzing will be observed as carbon dioxide is released. The carbon dioxide can be tested for with limewater
  • What is produced when carboxylic acids react with bases?
    A salt and water
  • What is produced when carboxylic acids react with carbonates?
    A salt, carbon dioxide, and water
  • What is produced when carboxylic acids react with hydrogencarbonates?
    A salt, carbon dioxide and water
  • How do alcohols react with carboxylic acids?
    Alcohol and carboxylic acids react to form esters, in a process called esterification.
  • What are the reaction conditions for esterification?
    • Heat
    • Sulfuric acid catalyst
  • When naming esters, what suffix is used?
    -anoate
  • Explain how ethanol can be separated from water:
    Ethanol and water have different boiling points and so distillation is a suitable technique