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1 Molecules
Biology Department
Watford Girls Grammar School
ntroduction
For each of the following you should be
able to:
Describe the properties
Know the general formulae & structure
Understand the role in animals & plants
waler
Caroorydrales
L|p|ds
Prole|rs
Nuc|e|c ac|ds
Water
Water is a polar molecule
t forms weak hydrogen bonds
t remains a liquid over a wide
temperature range
Water molecules stick to one another =
cohesion (surface tension)
Water molecules stick to other
substances = adhesion (capillarity)
Water
t has a high specific heat capacity so
water can maintain a reasonably
constant temperature (homeostasis)
t has a high latent heat of vaporisation
so animals use water to cool
themselves
t is less dense as a solid (ice).
. and ice is a poor conductor
Water is a good solvent
arbohydrates
ontain the elements arbon
Hydrogen & Oxygen
There are 3 types:
Monosaccharides
Disaccharides
Polysaccharides
Monosacharides
(H
2
O)
n
f n=3, triose (glyceraldehyde)
f n=5, pentose (fructose, ribose)
f n=6, hexose (glucose, galactose)
Monosaccharides are used for
Energy
Building blocks
C C
C
C
C
C
somerism
They can exist as isomers:
- & . glucose
-
.
Disaccharides
Formed from two monosaccharides
Joined by a glycosidic bond
A condensation reaction:
glucose + glucose maltose
glucose + galactose lactose
glucose + fructose sucrose
ondensation reaction
C C
C
C
C
C
C C
C
C
C
C
ondensation reaction
C C
C
C
C
C
C C
C
C
C
C
ondensation reaction
C C
C
C
C
C
C C
C
C
C
C
ondensation reaction
C C
C
C
C
C
C C
C
C
C
C
d|saccrar|de
1,1 g|ycos|d|c oord
1 1
Polysaccharides
Polymers formed from many
monosaccharides
Three important examples:
Starch
Glycogen
ellulose
Starch
nsoluble store of glucose in plants
formed from two glucose polymers:
Amylose
-glucose
1,4 glycosidic bonds
Spiral structure
Amylopectin
-glucose
1,4 and some 1,6
glycosidic bonds
Branched structure
Glycogen
nsoluble compact
store of glucose in
animals
-glucose units
1,4 and 1,6
glycosidic bonds
Branched structure
ellulose
Structural polysaccharide
in plants
.glucose
1,4 glycosidic bonds
Hbonds link adjacent
chains
ipids
Made up of , H and O
an exist as fats, oils and waxes
They are insoluble in water
They are a good source of energy
(38kJ/g)
They are poor conductors of heat
Most fats & oils are triglycerides
Triglycerides
Formed by esterification.
.a condensation reaction between 3
fatty acids and glycerol:
|ycero|
C
C
Fatty acids
arboxyl group (OOH)
attached to a long nonpolar
hydrocarbon chain (hydrophobic):
C C
C C
C
C
|ycero|
Fally ac|d
Esterification
C
C
|ycero|
Fally ac|d
Esterification
C
C
|ycero|
Fally ac|d
Esterification
C
C
sler oord
Waler
Esterification
This happens three times to form a
triglyceride:
g|ycero|
lally ac|ds
Phospholipids
One fatty acid can be replaced
by a polar phosphate group:
g|ycero|
ydroproo|c lally ac|ds
rydropr|||c
prosprale
Functions of lipids
Protection of vital organs
To prevent evaporation in plants &
animals
To insulate the body
They form the myelin sheath around
some neurones
As a water source (respiration of lipids)
As a component of cell membranes
Proteins
Made from H O N & sometimes S
ong chains of amino acids
Properties determined by the aa
sequence
Amino acids
N C
#
=20 aa
Glycine R=H
Alanine R=H
3
ar|re
carooxy|
Peptide bonding
N C
N C
#
Peptide bonding
N C
N C
#
Peptide bonding
N C
N C
#
Peptide bonding
C
N C
N C
#
Waler
Pepl|de oord
cordersal|or reacl|or
Peptide bonding
C
N C
N C
#
d|pepl|de
Primary structure
The sequence of aa is know as the
primary structure
The aa chain is a polypeptide
Secondary structure
Hbonding forms between the OOH
and the NH
2
of adjacent aa
This results in the chains folding:
Secondary structure
-re||x .p|ealed sreel
Tertiary structure
Bonding between Rgroups
gives rise to a 3D shape
Hbonds =O HN
onic bonds NH
3
OO
Disulphide bridge
H
2
SSH
2