ESTER, FAT & OILS Flashcards
How are esters formed?
condensation reaction between an alcohol and carboxylic acid - known as esterification
Esters in water
Have characteristic smells and are insoluble in water
Ester function group
O=C- O with R on C and single bonded O (-COO)
Main use of esthers
Flavourings and perfumes can also be used in chemicals industry as solvents
Make an esther structure
Hydrogen atom must be removed from hydroxyl group (-OH) of alcohol
OH from carbocyclic acid removed
Product of esther formation
Water
Naming ester
C=O comes from acid
change alcohol end to -yl
change acid end to -oate
alcohol name at front and acid at end
Fat
do not have same degree of distortion and pack closer together for increased mp
Hydrolysis of esters
break up ester by heating with ALKALI such as sodium hydroxide
water molecule added
OIls
liquid at room temp
more CC double bonds than fats (solid at room temp)
lower mp due to higher degree of unsaturated
double bonds distorts long fatty acid chains and molecules shapes - cannot pack close together
LDF fat and acids
poorer packing in oils so weaker
how is glycerol obtained
hydrolysis - hydrolysed by NaOH
reaction for hardening oils
addition - hydrogenation
test for level of unsaturation
Br - decolourises with double bonds (unsaturation)