Biological molecules: Monomers+Carbohydrates Flashcards
(49 cards)
Define polymer.
Give three examples.
Molecules formed when many monomers join together through condensation reactions (where a chemical bond forms between two molecules and a water molecule is released) .
-polysaccharides
-proteins
-DNA/RNA
Define monomer.
Give three examples.
Monomers are smaller units from which larger molecules are made. E.g.
-monosaccharides(glucose, fructose, galactose)
-nucleotides
-amino acids
What happens in a condensation reaction?
a chemical bond forms between two molecules and a water molecule is released.(When showing a condensation reaction ensure to put a water molecule as the product)
What happens in a hydrolysis reaction?
A water molecule is used to break the chemical bond between two molecules.
What monomers are carbohydrates made from?
Monosaccharides which are the molecules from which larger carbohydrates are made’
State four(common) hexose monosaccharides.
-Alpha glucose
-Beta glucose
-Galactose
-Fructose
Recall the structures of the two isomers of glucose.
-Alpha glucose (OH group on bottom)
-Beta glucose (OH group on top)
A condensation reaction between two monosaccharides forms a….
(1,4or 1,6) glycosidic bond
Describe how disaccharides form
A condensation reaction between two monosaccharides forms a glycosidic bond and releases a water molecule
Name three disaccharides and their monomers.
A condensation reaction between…+…=
-maltose = alpha glucose + alpha glucose
-sucrose = fructose + alpha glucose
-lactose = glucose and galactose
Describe Benedict’s test for reducing sugars
- Add an equal volume of Benedict’s reagent to a sample.
- Heat the mixture in an electric water bath at 100℃ for 5 mins.
- Positive result: colour change from blue to orange & brick-red precipitate forms.
Describe the Benedict’s test for non-reducing sugars.
- Heat sample with Benedict’s reagent and get a negative result.
2.Hydrolyse non-reducing sugar(into its reducing sugar monomers) by heating it with dilute hydrochloric acid then neutralise sample by adding sodium hydrogencarbonate.
3.Proceed with benedict’s test as normal.
Examples of reducing sugars.
All monosaccharides and some disaccharides e.g maltose and lactose
Example of a non reducing sugar
Sucrose
How would you prepare a solution if the sample is solid.
Crush the solid with water then filter out the solid.
What should you do to ensure that all the sugar reacts?
Use an excess of benedict’s solution
How are the samples heated
Always heated in a boiling water bath (could be electric)
How are polysaccharides formed?
Polysaccharides are formed when more than two monosaccharides are joined together by condensation reactions.
Name the monomers of the three polysaccharides.
glycogen
starch
cellulose
formed through the condensation of:
-alpha glucose
-alpha glucose
-beta glucose
Describe structure and function of glycogen
Mainly a storage polymer (acts as an energy store) of a-glucose in animal cells (but also found in plant cells):
- 1,4 and 1,6 glycosidic bonds
- branched = stored glucose can be released quickly which is important for energy release in animals.
- Insoluble = no osmotic effect and does not diffuse out of cells.
- compact = good for storage
(similar to amylopectin except it has more side branches coming off it)
Describe structure and function of starch
Storage polymer of alpha glucose in plants
insoluble=no osmotic effect on cells
large= does not diffuse out of cells
Describe a method to test for the presence of starch and state what a positive and negative result will look like.
-Add iodine dissolved in potassium iodide solution to the test sample.
- If starch is present, the sample changes from browny-orange to a dark black blue colour,
Describer structure and function of amylose
-Long unbranched chain of alpha glucose
-1,4 glycosidic bonds
-helix structure with intermolecular hydrogen bonds which help hold amylose in its helical structure= compact so good for storage
Describe structure and function of amylopectin
-long branched chain of alpha glucose= many terminal ends for hydrolysis into glucose so glucose can be released quickly
-1,4&1,6 glycosidic bonds