12.1 CARBOHYDRATES Flashcards
WHAT IA A MONOMER?
Small identical or similar molecules which can be condensed (joined or inked together) to make larger molecules called polymers
EXAMPLES- Amino Acids, Monosaccharides and nucleotides
POLYMER
They are large molecules from joining many ( 3 or more) identical or similar monomers together.
EXAMPLES - DNA, RNA, starch and haemoglobin
HOW A BOND IS FORM?
A condensation reaction joins the 2 molecules together with the formation of a chemical bond and involves the elimination of a molecule of water. This is catalysed by an enzyme. H2O is removed.
common monosaccharides
glucose, galactose and fructose
Disaccharides and example
Disaccharides (dimer) are formed by condensation of 2 monosaccharides
Eg. Maltose, Lactose
and Sucrose
Maltose
2 Alpha glucose
Lactose
Alpha glucose + Galactose
Sucrose
Alpha Glucose + Fructose
condensation equation
C6H12O6 + C6H12O6 ——→ C12H22O11 + H2O
Reducing sugar test
Add (equal volume/ 2cm^3) Benedict’s solution and heat
A coloured changed from Blue to green/yellow/orange/red
precipitate indicates the presence of a reducing sugar If there is NO CHANGE in colour there could be a non-reducing sugar present.
Describe how a student would show the of reducing sugars were present in solution
Add equal volumes of Benedict’s solution;
Heat to 95°C
Red/orange/
yellow/green precipitate (shows reducing sugar is present)
Non-reducing sugar test
- Heat a sample with acid for a few minutes to hydrolyse the glycosidic bond then neutralise the solution with an alkali. Acid = HCL Alkali = Sodium hydrogen carbonate
- Heat again with Benedict’s reagent
- Brick red precipitate shows a positive result ( for non resulting sugar)
Unknown conc of sugars
Benedict test (semi-quantitive) test for sugars as it only gives you an idea if sugars are present due to the colours but not the concentration.
colorimeter is quantitive as it measures that intensity of light passing through the solution/sample.
Increasing the amount of sugars increase the mass of the precipitate.
Standardising the method
Samples should always be shaken before testing
Zero the colorimeter before use (with a control)
Use the same filter throughout
Use same volume for each reading
TO DETERMINE CONC OF UNKNOWN SOLUTION
Make up several known conc of maltose/ glucose/ maltose/ lactose/ fructose
Carry out the Benedict’s test on each sample
Take readings of absorbance/transmission using a colorimeter
Plot readings to produce a graph called a calibration curve with
X axis —> concentration of named sugar/ mol dm-3
Y axis ^^ absorbance/transmission /
AU/%
Draw the line of best fit