bio practical Flashcards
iodine test
Use (x) drops of iodine on experimental area
If iodine is present: yellowish brown > blue-black
Iodine absent: remains yellowing brown
test for reducing sugars
2 cm of solution + 2cm benedicts solution
Soak in water bath until colour does not change further / for 5 mins
Solution Remains Blue : No Reducing Sugars
Blue > Green : Traces Of Reducing Sugars
Blue > Yellow/Orange ppt. : Moderate Amount Of Reducing Sugars
Blue > Brick-red ppt. : Large Amount Of Reducing Sugars
non reducing sugars
sucrose and polysaccharides
test for proteins
Use equal volume of biuret reagent in a test tube of sample
If solution turns violet, proteins are present.
solution remains blue, proteins are absent.
test for fats
ethanol emulsion
Sample + Ethanol + Water (In this order!)
2 immiscible layers formed, cloudy white emulsion/suspension forms at top of solution, fats are present
solution remains clear, fats are absent
Sodium hydrogencarbonate (NaHCO₃) purpose
supplies CO2
Soda-lime/Potassium hydroxide purpose
removes CO2
graph drawing axis reminders
Remember the d.p. of the scale units!!
Fully label the axes!!
graph drawing
Mostly don’t extend the curve beyond the points given
organelles that can be seen under light microscope
nucleus, cytoplasm, cell membrane, chloroplasts and cell wall
cutting specimen
eg, longitudinal, transverse, cross-sectioned, etc. TRANSVERSE MEANS CROSS SECTION
planning question
- state variables: 1 independent, 1 dependent, 3 constant
- apparatus used
- procedure
- control experiment + purpose
- outcomes
- - Reliability/Accuracy: repeat and obtain average results
plants test for photosynthesis reminder
keep in dark for eg 12h to destarch the plant
hazard of procedure
acid/base- corrosive substance // wear safety goggles to prevent splashes into eye
magnification calc
Drawing/Actual (1 d.p.)
sample drawing
- as accurately and as detailed as possible
- Dotted line along both ends of the longest axis, draw line between them and write measurement
- Measure sample along same transect
experimental errors : bubble counting
- Size of bubbles may vary, volume of gas produced will not proportional to the number of gas bubbles observed
Improve: Collect volume of gas produced
experimental errors : colour change
Subjectivity, different people may perceive the change differently. Eg. ppl perceive diff colourless, stop watch at diff times
Improve: Compare to standards (eg tube of water for colourless, use colourimeter
experimental errors : temp not maintained
- Will interfere with results (Especially with experiments dealing with enzymes, rate of reaction, etc.)
Improve: Use a thermostatically controlled water bath/keep checking temp of the water with thermometer, add more hot/cold water when needed
dp reminders
Magnification = 1 d.p. (dp of instrument used)
Temperature (°C) = 1 d.p.
Mass (g) = 2 d.p. (e.g. 0.01g, 5.83g, etc.)
ensuring accuracy: reading volume
Reading meniscus at eye level: reduce parallax error
ensuring accuracy: syringe air bubbles
Ensure no air bubbles in syringe : tapping syringe barrel then slowly pushing the piston to to release the bubbles
ensuring accuracy: apparatus contamination
Wash syringes with distilled water before using it to measure and transfer another solution
outliers when calculating mean
Anomalous results/ outliers should not be used to calculate the mean → injaccurate results
yeast reminder
glucose is simple sugar, most easily metabolised by yeast cells. Has enzymes to break down sucrose into glucose (sucrose), but not lactase for lactose.
glucose –> ethanol, co2
yeast reminder
glucose is simple sugar, most easily metabolised by yeast cells. Has enzymes to break down sucrose into glucose (sucrose), but not lactase for lactose.
glucose –> ethanol, co2
co2 reminder
remember it forms a weak acid when dissolved in water - carbonic acid (pH change)
apparatus accuracy
Use of 1cm3 syringe instead of 10cm3 (not precise enough to measure small quantities)
Use burette/micropipette
experimental error: using a lamp
using a lamp: not the only source of light in the lab - rate of psis faster than actual → inaccurate (incr LI → incr psis)
Why stain cells?
Stain to enhance clarity of cells when viewed under a light microscope
Why calculate % of a cell plasmolysed?
Cells are of diff sizes, a percentage is more accurate
control setups
— acts as a control setup / provides basis of comparison
Shows (whatever change the experiment brings about eg. shows that iodine turns blue-black w starch)
h2o2 reminder
h2o2 decomposes spontaneously when left in booking tube
Store in low temps/ cover beaker with al foil abd pour only when exp start
incr reliability
take another set of readings, average them
starch reminder
starch suitable storage - larger molecule (cannot diffuse thru cell membrane, hence retain in cell); easily hydrolysed back into glucose when required; insoluble in water (does not change water potential);