1
Q

iodine test

A

Use (x) drops of iodine on experimental area

If iodine is present: yellowish brown > blue-black
Iodine absent: remains yellowing brown

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2
Q

test for reducing sugars

A

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

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3
Q

non reducing sugars

A

sucrose and polysaccharides

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4
Q

test for proteins

A

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.

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5
Q

test for fats

A

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

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6
Q

Sodium hydrogencarbonate (NaHCO₃) purpose

A

supplies CO2

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7
Q

Soda-lime/Potassium hydroxide purpose

A

removes CO2

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8
Q

graph drawing axis reminders

A

Remember the d.p. of the scale units!!
Fully label the axes!!

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9
Q

graph drawing

A

Mostly don’t extend the curve beyond the points given

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10
Q

organelles that can be seen under light microscope

A

nucleus, cytoplasm, cell membrane, chloroplasts and cell wall

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11
Q

cutting specimen

A

eg, longitudinal, transverse, cross-sectioned, etc. TRANSVERSE MEANS CROSS SECTION

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12
Q

planning question

A
  1. state variables: 1 independent, 1 dependent, 3 constant
  2. apparatus used
    - procedure
    - control experiment + purpose
    - outcomes
    - - Reliability/Accuracy: repeat and obtain average results
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13
Q

plants test for photosynthesis reminder

A

keep in dark for eg 12h to destarch the plant

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14
Q

hazard of procedure

A

acid/base- corrosive substance // wear safety goggles to prevent splashes into eye

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15
Q

magnification calc

A

Drawing/Actual (1 d.p.)

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16
Q

sample drawing

A
  • 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
17
Q

experimental errors : bubble counting

A
  • 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

18
Q

experimental errors : colour change

A

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

19
Q

experimental errors : temp not maintained

A
  • 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

20
Q

dp reminders

A

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.)

21
Q

ensuring accuracy: reading volume

A

Reading meniscus at eye level: reduce parallax error

22
Q

ensuring accuracy: syringe air bubbles

A

Ensure no air bubbles in syringe : tapping syringe barrel then slowly pushing the piston to to release the bubbles

23
Q

ensuring accuracy: apparatus contamination

A

Wash syringes with distilled water before using it to measure and transfer another solution

24
Q

outliers when calculating mean

A

Anomalous results/ outliers should not be used to calculate the mean → injaccurate results

25
Q

yeast reminder

A

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

25
Q

yeast reminder

A

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

26
Q

co2 reminder

A

remember it forms a weak acid when dissolved in water - carbonic acid (pH change)

27
Q

apparatus accuracy

A

Use of 1cm3 syringe instead of 10cm3 (not precise enough to measure small quantities)
Use burette/micropipette

28
Q

experimental error: using a lamp

A

using a lamp: not the only source of light in the lab - rate of psis faster than actual → inaccurate (incr LI → incr psis)

29
Q

Why stain cells?

A

Stain to enhance clarity of cells when viewed under a light microscope

30
Q

Why calculate % of a cell plasmolysed?

A

Cells are of diff sizes, a percentage is more accurate

31
Q

control setups

A

— 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)

32
Q

h2o2 reminder

A

h2o2 decomposes spontaneously when left in booking tube
Store in low temps/ cover beaker with al foil abd pour only when exp start

33
Q

incr reliability

A

take another set of readings, average them

34
Q

starch reminder

A

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);