Exam Flashcards
triacylglycerols function
fats and oils, energy storage
phospholipids and sterols function
formation of biological membranes
glycolipids
sugar and lipids, cell membranes
lipoproteins
associated with cardiovascular disease
saturated fatty acids
no double bonds
unsaturated fatty acids
one or more double bonds
commonly occurring saturated fatty acids
laurate-12, myristate-14, palmitate-16, stearate-18, arachidate-20
as saturated chain length increases
melting point increases, solubility decreases
carboxylic acids + alcohol
ester
carboxylic acid + acid
anhydrides
triacylglycerols (TAGs)
majority, linking 3 fatty acids to glycerol through ester linkage, very hydrophobic
simple TAGs
same fatty acid in all 3 positions
mixed TAGs
2-3 different fatty acids
phosphoric acid + alcohol/acid
phosphate esters and phosphoanhydrides
glycerophospholipids/phosphoglycerides
2 fatty acid tails and 1 polar head, differentiates from TAG and allows them to form lipid bilayers
phosphatidylcholine/lecithin
glycerophospholipid, different combinations of fatty acids at R1 and R2
micelle
smallest lipid aggregate, units are wedge shaped
bilayer
hydrophobic tails too bulky to form micelles
vesicle
bilayers folded back onto themselves
analysis of lipids
separated on polarity, TLC plate, less polar move further
monosaccharide chemical structure
- carbonyl group, either aldehyde or ketone
- 2 Cs with hydroxyl/alcohol group
aldoses
monosaccharide with aldehyde
ketoses
monosaccharide with ketone
fischer projection formula
vertical bonds project behind, horizontal bonds project out
perspective formula
dashed bonds point away, solid wedge project Infront
chiral carbon
carbon bonded to 4 different groups
enantiomers
mirror images, identical chemical properties, opposite polarization
diastereomers
monosaccharides with more than 1 chiral carbon, different chemical properties
D sugar
chiral carbon furthest away from carbonyl group has same configuration as D-glyceraldehyde (OH on right)
epimer
identical except for configuration at 1 C, special case of diastereomers
sugar with n chiral centers has
2^n stereoisomers, half L half D