What elements are carbohydrates made of
Carbon, hydrogen, oxygen
3 types of carbohydrates
Monosaccharides, disaccharides, polysaccharides
Name 3 monosaccharides
glucose, fructose, galactose
Name 3 disaccharides
sucrose, maltose, lactose
Name 3 polysaccharides
Starch, cellulose, glycogen
What is the classification of monosaccharides based on
Number of carbon atoms
Chemical formula for glucose, fructose, galactose
C6H12O6
Chemical formula for sucrose, maltose, lactose
C12H22O11
General formula for monosaccharides
CnH2nOn
Single sugar is a
Monosaccharide
How many orientations can glucose be in
Any
How many structural isomers does glucose have
2
Structural isomer meaning
Same molecular formula, different structure
Draw alpha glucose
Draw beta glucose
a glucose + a glucose?
starch (storage molecule)
b glucose + b glucose?
cellulose (structure)
Describe a condensation reaction
Smaller monomer joins to another, water molecule is removed. Remainder = residue. Produces polymer (larger molecule)
What kind of bond does a condensation reaction create?
Covalent / glycosidic bond
Glycosidic bond
Chemical formed as a result of condensation between to monosaccharides
2 alpha glucoses create
maltose + water
beta fructose + alpha glucose
Sucrose + water
galactose + alpha glucose
lactose
molecular formula for lactose, maltose, sucrose
C12H22O11
What are carbohydrates used for
By body for fuels (respiration) and to build cells
Monomers join together to form
Polymers
Hydrolisis
opposite of condensation. Polymer broken down into molecules. Water is added
Starch’s monomer
monomer = alpha glucose, mixture of 2 polymers
starch digested by
amylase
2 polymers that make up starch
amylose, amylopectin
Amylose structure
curly (forms helix) to be compact. only a 1-4 glycosidic bonds
Amylopectin structure
Highly branched. a 1-6 + 1-4 glycosidic bonds. Lots of terminal starch molecules to allow many glucose units to be synthesised and stored effectively
Glycogens monomer
alpha glucose
Function of glycogen
storage of glucose which allows for fast energy release when needed and is present in muscle tissue
Function of starch
Store glucose for later energy use
Glycogen structure
1-4, 1-6 alpha glycosidic bonds. highly branched. compact to store more (coiled),
polymer = large molecule, insoluble, osmotically inert.
Branched molecule = many terminal glucose molecules = easily hydrolysed for energy released in respiration
Cellulose monomer
beta glucose
Chemical equation for respiration
6H12O6 + 6O2 → 6CO2 + 6H2O
glucose + oxygen -> carbon dioxide + water
Cellulose structure
beta glucose bonds 1-4, 1-6
alternate molecuules rotate 180 degrees
parallel chains cross linked to form microfibrils for strength. prevents osmotic lysis in hypotonic solutions
long straight chains
Similarities between starch and cellulose
C,H,O
carbohydrate
monomer: glucose
polysaccharide
alpha 1 -4 glycosidic bond
Other “polysaccharides”
Contain nitrogen
Chitin: fungal cell wall
Peptidoglycon (meurin): component of prokaryotic (bacteria) cell wall