AQA CHEMISTRY

    Cards (48)

    • What is the reagent in the electrophilic addition of water to an alkene?

      Water with strong acid (sulfuric or phosphoric acid)
    • What two species are added to the carbons either side of the double bond when water is electrophilically added to an alkene?

      H and OH
    • What is the product when water is electrophilically added to an alkene?

      An alcohol
    • What is the general formula of an alcohol with no carbon rings?

      CnH2n+1OH
    • Where is the OH attached in aromatic alcohols?

      Directly to the ring
    • What are aromatic alcohols known as?

      Phenols
    • What is a primary alcohol?

      One which is attached to a carbon which is attached to 1 other carbon
    • What is a secondary alcohol?

      One which is attached to a carbon which is attached to 2 other carbons
    • What is a tertiary alcohol?

      One which is attached to a carbon which is attached to 3 other carbons
    • What is the C-O-H angle in an alcohol and why?

      ~105° because the oxygen has two lone pairs which makes the functional group a V-shaped molecule
    • Why do alcohols have a much higher boiling point than alkanes with a similar molecular mass?

      Because they can form hydrogen bonds, which are not present in alkanes
    • Why do the boiling points of alcohols increase as chain length increases?

      Increased chain length leads to an increase in van der waals' forces
    • Why do the boiling points of alcohols decrease as branching increases?

      Because this weakens their van der waals' forces
    • Which types of alcohols are soluble in water and why?

      Those with short hydrocarbon chains because this allows the hydrogen bonding from the alcohol group to water molecules to dominate
    • Why aren't alcohols with long hydrocarbon chains soluble in water?

      Because unlike in short chain hydrocarbons the long, non-polar hydrocarbon chain dominates over the hydrogen bonding
    • What is the reagent in the dehydration of an alcohol?

      Concentrated sulfuric/phosphoric acid
    • What are the conditions of the dehydration of an alcohol?

      Reflux at 180°C
    • What is the product of the dehydration of an alcohol?

      Alkene
    • What is an alternative method to reflux with strong acid to dehydrate an alcohol?

      Pass vapour over a heated alumina (aluminium oxide) catalyst
    • Why can some alcohols not be dehydrated?

      Lack of an adjacent hydrocarbon
    • What is oxidation of alcohols used to differentiate between?

      Primary, secondary or tertiary alcohols
    • What is the usual reagent in the oxidation of alcohols?

      Acidified potassium (VI) dichromate
    • What are primary alcohols oxidised to?

      Easily to aldehydes, and then carboxylic acids
    • What are secondary alcohols oxidised to?

      Easily to ketones
    • What are tertiary alcohols oxidised to?

      Not oxidised under normal conditions, only break down under very vigorous oxidation
    • What is potassium dichromate usually oxidised with?

      Dilute sulfuric acid
    • What is it essential to do when making aldehydes from alcohols?

      Distill off the aldehyde before it is further oxidised to a carboxylic acid
    • What colour change do primary or secondary alcohols cause in potassium dichromate?

      Orange to green
    • What colour change do tertiary alcohols cause in potassium dichromate?

      None
    • What change in apparatus must be made to produce carboxylic acids instead of aldehydes?

      The Liebig condenser must be placed directly above the pear-shaped flask instead of to the side, so that any distilled aldehyde returns to the flask for further oxidation
    • What is the composition of methylated spirits?

      Ethanol, along with a small amount of poisonous methanol and a purple dye
    • What is an elimination reaction?

      One in which a small molecule leaves the parent molecule
    • What smell do most aldehydes and ketones have?

      A pleasant one
    • Are the physical properties of aldehydes and ketones similar?

      Yes
    • What 3 reactions suggest that burning ethanol is carbon neutral and why?

      Photosynthesis, fermentation and combustion of ethanol, because overall 6 carbon dioxides go in and 6 carbon dioxides come out
    • What is ethanol used as?

      A biofuel or as a solvent
    • What are 2 ways of producing ethanol?

      Hydration of ethene or fermentation of glucose
    • What are the reaction conditions of the hydration of ethene to make ethanol?

      Concentrated phosphoric acid catalyst, 300°C, 60 atm
    • How is over 90% of ethanol made?
      Fermentation using yeast
    • How is ethanol made using yeast?

      The yeast produces ethanol during anaerobic respiration, using glucose as its food
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