6.1.5: Reactions and uses of esters Flashcards
Properties of esters
3
sweet smell
polar liquids
low boiling points
Uses of esters
5
industrial solvents plasticiers colourings and flavourings paints glue
Two types of hydrolysis of esters
acid hydrolysis and base hydrolysis
Reverse esterification reaction
hydrolysis
base/acid
Acid hydrolysis
Splits the ester into a carboxylic acid and an alcohol by refluxing with a dilute acid (HCl/H2SO4)
What is necessary in acid hydrolysis reactions
and why
lots of water to push equilibrium to the right
Base hydrolysis
Reflux the ester with a dilute alkali (NaOH) to form a carboxylate ion and an alcohol
Lipids (animals fats and vegetable oils)
Esters of glycerol and fatty acids
Fatty acids are
long chain carboxylic acids
Types of fatty acids
2
saturated
unsaturated
Hydrolysis of fats and oils
base hydrolysis (NaOH) form glycerol and a carboxylate ion which combines with Na to form a sodium salt
Soap is a type of
sodium salt
Glycerol also known as
propane-1,2,3-triol
Converting sodium salt back into a long chain carboxylic acids
add an acid such as HCl
Biodiesel
vegetable oils react with methanol and a strong alkali catalyst (NaOH or KOH)
to form methyl esters (biodiesel) and glycerol
Biodiesel impact on environment
carbon neutral
However energy required to harvest, plant and transport them comes from fossil fuels so overall process isn’t neutral