1/26
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai | Chat |
|---|
No analytics yet
Send a link to your students to track their progress
Carbohydrates elements
carbon, hydrogen, oxygen (1:2:1)
Monosaccharides general formula
(CH2O)n
Alpha glucose
Beta glucose
Galactose
Diasaccharide reaction
Condensation reaction between two monosaccharides to form a glycosidic bond. Molecule of water is released.
Sucrose
made up of a-glucose and fructose
Lactose
made up of glucose and galactose
Maltose
made up of two glucose molecules
Test for reducing sugars
Benedict's test. A blue solution, add a few drops to your solution. Heat in a water bath and if reducing sugars are present the benedict's will turn brick red. Happens because reducing sugars reduce the copper(II) ions in Benedict's solution to copper(I) ions.
Test for non-reducing sugars
Heat with HCL then neutralise with sodium hydrogen carbonate, which produces monosaccharides needed to conduct a test with Benedict's solution.
What are reducing sugars?
All monosaccharides and some disaccharides (not sucrose)
process that splits glycosidic bonds
hydrolysis. Water is added
Starch compounds
amylose and amylopectin
Amylose structure
Linear polysaccharide
alpha 1-4 glycosidic bonds
Properties of amylose
Large surface area
Insoluble
Amylose function
Energy store
Provides structural stability
Used for slow release of glucose
Amylopectin structure
Branched Chains of alpha glucose 1-4 and 1-6 glycosidic bonds
Properties of amylopectin
More soluble in water than amylose
Digested more quickly
Functions of amylopectin
Branches of glucose are broken off for quick release of glucose when more energy is needed
Glycogen structure
Branches have alpha(1,6) bonds which can be broken off for quick release of glucose Linkages have alpha(1,4) bonds.
Compact
lipid structure
glycerol and 3 fatty acids (triglyceride) combined using ester bonds
difference between fats and oils
Fats are solid at room temperature and oils are liquid at room temperature
glycerol chemical formula
C3H8O3
saturated fatty acid
Fatty acid with no carbon-carbon double bonds.
unsaturated fatty acid
Fatty acid with one or more carbon-carbon double bonds.
Ester bond
formed in condensation reaction between carboxyl (-COOH) of fatty acid and hydroxyl group (-OH) of glycerol called esterification