4.2.1 Alcohols Flashcards
(27 cards)
what functional group do alcohols contain
- hydroxyl OH
what is the general formula of an alcohol
- CnH2n+1 OH
what are some general differences in physical properties between alcohols and alkanes with the same number of carbon atoms
- alcohols are less volatile, higher mp/bp and greater water solubility
what is the reason for differences in physical properties between alcohols + alkanes with same no of C
- alkanes have non-polar bonds as electronegativity of H and C very similiar
> alkane = non polar so very weak London forces - alcohol has polar O-H bond because of electronegativity difference
> alcohol = polar so have weak LF + stronger hydrogen bonds between polar O-H
why do alcohols have high mp + are less volatile
- hydrogen bonds between OH require lots of energy to overcome
are alcohols soluble in water + why
- soluble in water
> hydrogen bonds form between the polar OH group of alcohol and water molecules
what happens to solubility as the hydrocarbon chain in alcohol increases
- solubility decreases
> influence of the OH polarity decreases and solubility of longer chains decreasw
why are alcohols very good solvents
- can dissolve both polar and non-polar molecules
what are the 3 different ways alcohols can be classified as
- primary
- secondary
- tertiary
alcohols can undergo combustion to produce what
- CO2 + H2O
> releases heat
which types of alcohols can be oxidised
- primary + secondary
what can alcohols be oxidised by
- an oxidising agent
what can primary alcohols be oxidised to
- aldehyde
- carboxylic acid
how can you make an aldehyde from an alcohol
- oxidation of primary alcohol
- heat + distill with acidified potassium dichromate (oxidising agent)
> aldehyde formed
what happens to dichromate ions in oxidation of alcohols
- reduced from orange to green
how do you prevent oxidation of aldehyde into carboxylic acid
- aldehyde removed by distillation as its formed
> aldehyde has has lower boiling point than alcohol
why do aldehydes have lower bp than alcohols
- because they don’t have hydrogen bonds
how can you form a carboxylic acid from an alcohol
- primary alcohol heated strongly under reflux with excess of acidified potassium dichromate
why do you need excess oxidising agent for formation of carboxylic acid
- to ensure that all of the alcohol is oxidised
what does a secondary alcohol oxidise to form
- ketones
how can you form a ketone from an alcohol
- secondary alcohol oxidised under reflux with acidified potassium dichromate
what can tertiary alcohols oxidise to from
- nothing
- tertiary alcohols do not undergo oxidation reactions
what is dehydration
- a reaction in which a water molecule is removed from a starting material
how do alcohols undergo dehydration + what forms
- alcohol heated under reflux with acid catalyst e.g. conc sulfuric acid or phosphoric acid
- product is an alkene