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why is water polar
the O atoms attract more electrons making them slightly negative whereas the H atoms have a slight positive charge
hydrophilic
a molecule that is attracted to water. these molecules are either charged or polar and can dissolve in water. e.g. salt or glucose
hydrophobic
a molecule that is repelled by water. these molecules are non polar and cant dissolve in water. e.g. oil
what is a hydrogen bond
a weak interaction that can occur wherever molecules contain a slightly negatively charged atom bonded to a slightly positively charged hydrogen atom
10 properties of water
liquid at room temperature
high latent heat of evaporation
high specific heat capacity
low density of ice
cohesion
adhesion
surface tension
water acts as a solvent
water is transparent
reactant
biological molecules =
carbon based molecules that make up living organisms
elements present in carbohydrates
carbon
hydrogen
oxygen
elements present in proteins
carbon
hydrogen
oxygen
nitrogen
sometimes sulfur
elements present in nucleic acids
carbon
hydrogen
oxygen
nitrogen
phosphorus
elements present in lipids
carbon
hydrogen
oxygen
mono
1
di
2
poly
many
sacchar
sugar
polymer
is a large molecule made from many smaller repeating molecules of the same monomer
polymerisation
formation of a polymer
monomer
a small molecule which binds to many other identical molecules to form a polymer
dimer
2 monomers joined together
polymer
a large molecule made from many smaller molecules called monomers
sharing one pair of electrons
single covalent bond
sharing 2 pairs of electrons
double covalent bonds
condensation reaction
removal of water to make polymer
hydrolysis reaction
addition of water to split polymer
functions of carbohydrates
energy source e.g. glucose
energy store e.g. starch or glycogen
structure e.g. cellulose in plant cell walls
also part of other molecules such as nucleic acids, glycoproteins, glucolipids
why are carbohydrates called hydrated carbon
in monosaccharides there are 2 hydrogen atoms and one oxygen for every one carbon in the structure (ch2o)n
monosaccharides single sugars
glucose - 6c (hexose)
ribose - 5c(pentose)
monosaccharides key features
simplest carbohydrate with single sugar units
important as an energy source (C-H bonds)
have between 3-7 carbon atoms
sweet tasting
soluble in water but insoluble in non polar solvents
disaccharide double sugars
sucrose - alpha glucose + fructose
maltose - alpha glucose + alpha glucose
lactose - alpha glucose + galactose
polysaccharide chains of many sugars
starch - lots of alpha glucose
glycogen - lots of alpha glucose
cellulose - lots of beta glucose
whats the difference between a hexose and pentose monosaccharide
in a hexose sugar theres 6 carbons but in a pentose sugar theres 5 carbons
name of monosaccharides that make up maltose
alpha glucose + alpha glucose
name of monosaccharides that make up sucrose
alpha glucose + fructose
name of monosaccharides that make up alpha lactose
(beta) galactose + alpha glucose
name of monosaccharides that make up beta lactose
(beta) galactose + beta glucose
name of monosaccharides that make up cellubiose
beta glucose + beta glucose
what type of reaction breaks up a polysaccharide into a disaccharide
hydrolysis
what type of reaction forms a disaccharide from monosaccharides
condensation
alpha glucose role in body
energy source
component of starch and glycogen which acts as energy stores
beta glucose role in body
energy source
component of cellulose which provides structural support in plant cell walls
ribose role in body
component of ribonucleic acid (RNA), ATP, and NAD
deoxyribose role in body
component of deoxyribonucleic acid (DNA)
key features of polysaccharides
made up of 100s or 1000s of repeating monosaccharide subunits
formed by repeated condenssation reactions
can be broken down by hydrolysis using enzymes
polysaccharides are not sugars and dont taste sweet
polysaccharides are insoluble in water
to break down starch you need
amylase to break down = 1,4 glycosidic bonds and
glucosidase to break down = 1,6 glycosidic bonds
amylose function
energy store in plants
amylose structure
unbranched
polysaccharide twists to form helix
amylose glycosidic bonds
alpha - 1,4 glycosidic bonds only
amylose extra detail
hydrogen boding present within structure for further stabilisation
compact
can store a lot of glucose in a small space
amylopectin function
energy store in plants
amylopectin made of
alpha glucose
amylopectin structure
polysaccharide chains coiled into helix
branching present
amylopectin glycosidic bonds
alpha - 1,4 and 1,6
amylopectin extra details
hydrogen bonding present within structure for further stabilisation
compact
greater surface area for enzyme action and therefore more rapid hydrolysis
glycogen made of
alpha glucose
glycogen structure
polysaccharide chains coiled into helix
lots of branching present(far more than amylopectin) and more alpha - 1,6 glycosidic bonds
glycogen glycosidic bonds
alpha 1,4 and 1,6
glycogen extra detail
hydrogen bonding present within structure for further stabilisation
compact
highly branched
can be very rapidly hydrolysed
more branches = more ends = more hydrolysis = more glucose for energy (respiration)
describe the importance of polysaccharides being insoluble
polysaccharides act as energy storage molecules
by being large and insoluble it means that they are able to perform such structural roles without being dissolved in cytoplasm
why is glycogen a good storage molecule
insoluble
does not affect water potential
can be broken down quickly by hydrolysis
lots of branches
compact
high energy content for mass
is amylose humans or plants
plants
where is amylose stored
starch grains in plant cells vacuole
is amylose a form of starch
yes
whats the monomer of amylose
alpha glucose
is amylose branched
no
is amylose soluble
no
what type of glycosidic bonds does amylose have
alpha - 1,4
is amylose spiralled
yes
are H bonds important in amylose
yes
is amylopectin humans or plants
plants
where is amylopectin stored
starch grains in plant cells vacuole
is amylopectin a form of starch
yes
what is the monomer of amylopectin
alpha glucose
is amylopectin branched
yes
is amylopectin soluble
no
what type of glycosidic bonds does amylopectin have
alpha - 1,4 and 1,6
is amylopectin spiralled
yes
are H bonds important in amylopectin
yes
is glycogen humans or plants
humans
where is glycogen stored
glycogen granules in cells like the liver
is glycogen a form of starch
no
what is the monomer of glycogen
alpha glucose
is glycogen branched
yes
is glycogen soluble
no
what type of glycosidic bonds does glycogen have
alpha - 1,4 and 1,6
is glycogen spiralled
yes
are H bonds important in glycogen
yes
role of cellulose
to provide structure, has a high tensile strength, insoluble, unreactive and inflexible
where is cellulose found
in a plant cell wall
what is cellulose
a structural carbohydrate
what is cellulose made of
beta glucose
what do we use cellulose as
a fibre source
what glycosidic bonds does cellulose have
beta - 1,4
why is cellulose not spiralled
has inverting alternate beta glucose molecules which prevent spiralling
H bonds exist between glucose molecules within the same chain
H bonding exists between glucose molecules in different chains
how is cellulose packed into fibres in the cell wall
around 60 cellulose chains become cross linked by hydrogen bonds to form microfibrils
microfibrils are held together by further hydrogen bonds to form microfibrils and groups of microfibrils combine to form fibres
pectin acts like glue
whats the role of chitin
functions as a structural polysaccharide forming insect and crustacean exoskeletons and fungi cell wall
forms long parallel chains of acetyleosein in similar ways to cellulose
whats the structure of chitin
has an acetylamino group rather than a hydroxyl group on C2
whats the role of peptidoglycan
bacterial cell walls
whats the structure of peptidoglycan
this is made from long polysaccharide chains that lie in parallel, cross linked by short peptide chains
where do lipids come from
animals and vegetable sources
what aren’t lipids like proteins and carbohydrates
polymers
what elements do lipids contain
carbon
hydrogen
oxygen