lipids Flashcards

1
Q

solubility of lipids

A

insoluble in water and polar solvents
soluble in non-polar solvents

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2
Q

4 functions of lipids

A

storage
- stores energy in fats and oils

structural
- protection
- insulation
- membranes

metabolism

industrial uses

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3
Q

structure of fatty acids

A

hydrophobic hydrocarbon tail - non-polar
hydrophilic carboxyl group head - polar

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4
Q

short chain fatty acids

A

2-5 carbon atoms
byproduct of fermentation
weak acids
- some polar properties

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5
Q

long chain fatty acids

A

more than 5 carbons
naturally occurring in even number of carbons
saturated or unsaturated
- very little polar properties

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6
Q

examples of short chain fatty acids (4)

A

2 - ethanoic acid - acetic acid
3 - propanoic acid - propionic acid
4 - butanoic acid - butyric acid
5 - pentanoic acid - valeric acid

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7
Q

examples of long chain fatty acids (2)

A

saturated

16 - hexadecanoic acid - palmitic acid - 60.7
18 - octadecanic acid - stearic acid - 69.6

unsaturated

18:1 delta 9 - oleic acid - 16
18:2 delta 9,12 - linoleic acid - -5
18:3 delta 9,12,15 - a-linolenic acid - -11

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8
Q

saturated fatty acids

A

no c=c double bonds
packed closely and interact
longer chain = more interactions
increase melting point when longer

eg hexdecanoic acid
octadecanic acid

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9
Q

unsaturated fatty acids

A

1 or more c=c double bond
not straight, bond creates kink
cannot pack closely so fewer interactions
each double bond lowers melting point

cis or trans configurations
trans - hydrogen placed across double bond
cis - hydrogen on same side of double bond (normal)

eg oleic acid
linoleic acid
a-linolenic acid

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10
Q

structure of triacylglycerols

A

3 fatty acids joined to a glycerol
by an ester bond

neutral molecules
used a energy stores
- seeds of oilseed plants
- adipose tissue of animals

hydrogen of hydroxyl group of glycerol reacts with OH of fatty acid

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11
Q

why do tags make an efficient energy store? (4)

A

high energy in low weight
- long hydrocarbon chains give high energy

high energy in low volume
- neutral, packed closer than charged molecules, less volume

readily stored and released in hydrolysis and condensation

stores easily distinguish from surrounding material
- non-polar hydrophobic creates lipid droplets

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12
Q

4 reactions of triacyglycerols

A

hydrolysis
iodination
saponification
hydrogenation

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13
Q

hydrolysis of triacyglycerols

A

breaking of a covalent bond by the addition of water

essential before energy can be obtained
catalysed by specific lipase enzymes
broken down into glycerol and 3 fatty acid chains

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14
Q

iodination of triacyglycerols

A

iodine reacts with double bonds in unsaturated chains

interactions breaks double bond and iodine atom bound to each carbon
(hydrogen removed)

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15
Q

saponification of triacyglycerols

A

formation of soap by heating a triacylglycerol with alkali
fatty acids released

occurs when react with strong bases
releases glycerol molecule

forms salts of fatty acids known as soap

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16
Q

salts of fatty acids produced in saponification

A

soap formed is amphipathic

allows molecules to form micelles
hydrophobic chains pack together inside
hydrophilic face outwards towards solvent

gives soap its cleaning properties
dirt enclosed within micelle

17
Q

hydrogenation of triacyglycerols

A

hydrogen reacts with hydrocarbon chain
double bond broken and hydrogen attaches

removes double bond
increases proportion of saturated fatty acids
increases melting point

18
Q

use of hydrogenation

A

transform oil and fats that are liquid at room temperature - hardened

partial hydrogenation used to improve shelf life
cis double bond converted to trans double bond
= trans fatty acids

19
Q
A