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IGCSE Biology Paper 6 Tips! - IGCSE Guide

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IGCSE Biology Paper 6 Tips! - IGCSE Guide

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danayousif1711
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IGCSE GUIDE

IGCSE Biology
paper 6 tips!

Examiner’s tips for


biology paper 6

Biology paper 6
tips
ipro

This paper needs to analyze the


relationships between variables and
readings. The questions (topics) required
from paper 6 are:

1. Taking reading from instruments and apparatus


(measuring cylinder,
stopwatch, burette, gas syringe).
2. Measuring length by ruler (take care of required unit
cm or mm)
3. Calculate the magnification and the unit times ( X
)
4. Draw a suitable graph and must include the
following:
5. Appropriate scale.
6. Axes labeled and their units.
7. Plot all points by pencil then pen to be clear

a) Types of graph

– Line graph: when say ‘passing through


points’ or ‘suitable graph’ or ‘when there
is time as variable’. It can be straight
(best fit line) or smooth curve.

– Bar charts: when to compare

– Pie charts: when he draws a pie charts


and figure is given

7. Take readings from graph (Line


graphs) by extending line or curve.

8. Explain results: ethers directly or


inversely proportion and some details
from graph to support your answer.

9. To label some parts (palisade, xylem,


etc. )

10. Purpose of experiment: As control


experiment to compare results

11. Applying some formulas given to


you

12. Complete headings of a table ( g, cm


, s, etc.)

13. Counting and making tally tables

14. Calculate percentage increase or


decrease

15. Safety precautions (fume cupboard,


heat in hot water path, wear gloves and
googles)

16. Giving surface area by counting and


completing squares

17. Experimental accuracy


improvements:Using electronic balance
instead of spatula

Use larger number of sample


Using lid and polystyrene cup in heating experiment
– Using data logger instead of timer and stopwatch
To be fair and keep factors same and constant
Use burette instead of measuring cylinder
Common one: to repeat and take average (mean)
Same apparatus and instruments
Control temp and PH.

18. Classification of innervates (name of


group, feature)

19. Adaptations of animals (ex:


camouflage)

20. pH measured by universal indicator


and pH meter

21. Hydrogen carbonates indicator and


its color.
22. Round results always 2 or 3
significant figures

23. Giving ratios in simplest form.

24. Rate is always: volume of gas/time


taken.

25. Some observations to be recorded.

26. Leaving experiment after heating:

To avoid the effect of the previous one


To provide time to adapt temperature

27. In temperature-enzyme experiment:

Steps to follow are:

Same volume and concentrations of same reagents


Same of volume of same enzyme
Same apparatus used
Same time intervals
Control pH
Apply different temperatures.
Note readings and results
Plot them and compare
Repeat and take average.

28. Steps to follow in pH-enzyme


experiment:

Same volume and concentrations of same reagents.


Same of volume of same enzyme
Same apparatus used.
Same time intervals
Control temperature
Apply different pH
Note readings and results.
Plot them and compare
Repeat and take average

29. In germination experiments where


pH is a variable:

Use same seeds due to age and species


Use same number of seeds
Same of volume of same enzyme
Use same apparatus
Keep time intervals the same
Control temperature
Conduct experiments over different pHs
Note readings and results
Plot them and compare
Repeat and take average

30. Experiments where rate needs to be


calculated:

Add 2~3 cm3 of culture to test tube


Shake it
Connect test tube to gas syringe
Note gas volume
Control temperature
Record time taken by stopwatch

Plot them and compare


Repeat and take average of results

31. Variables to be constant in


experiments involving cooling:

Room temperature
Time interval
Temperature
Volume of water

32. To determine number of stomata:

View the leaf under microscope at high


magnification
Count the number of stomata
Determine the area of stomata
Calculate area of stomata (using a grid)

33. Determining the rate of uptake of


water by plants (transpiration rate)

Conditions to keep constant

Plant species
Number of plants
Volume of water
Time interval
Apparatus
Light intensity

Method

Control pH and temp.


Note readings
plot and compare
Repeats and take average

34. Making brief comparisons


(comprising of number, size, color,
presence of some special parts, shape,
surface area)

35. Drawing certain parts of plant/


animal:

Use a sharp HB pencil.


Draw a clear and similar shape.
Avoiding shading
Make accurate labels (at least 2)
Draw according to the magnification asked in the
paper.

36. Make biological tests: Scientists


often need to know whether or not a
particular type of molecules is present in
a solution. There are number of simple
chemical tests that can be carried out on
biological solutions.

a) A special test for lipids.

An important feature of fats and oils is


that they are insoluble in water. This
means that you cannot make an aqueous
solution of a fat or oil on which to carry
out a biochemical test. However, the fact
that lipids are insoluble forms the basils
of a physical test. This is known as the
emulsion test: How to?

2 cm3 of ethanol are added to the unknown solution,


and the mixture is gently shaken.
the mixture is poured into a test tube containing an
equal volume of distilled water.
If a lipid is present, a milky-white emulsion is
formed.

b. Testing for vitamin C using DCPIP.


Vitamin C takes the color out of a blue
dye called DCPIP.

The number of drops of vitamin C solution needed to


make this happen depends on how concentrated the
vitamin C solution is.
So, if few drops: strong vitamin C solution.
If many drops: weak vitamin C solution.

c. A control is needed to make sure that


results are valid:

-To show that the test is working


properly a solution that is known to the
substance is tested (for example, the
biuret reagent is used with a solution
known to contain protein). This should
give a result.

-To show that the test solutions are not


contaminated, each test should be
carried out on a sample of water. This
should give a negative result.

Examples:

To test for Protein, a few drops of Biuret reagent are


added to 2 cm3 of the unknown solution (to be tested
for containing protein) and the mixture is gently
shaken. A MASSIVE/PURPPLE color is a positive
result (protein is present)
To test for starch, a few drops of iodine solution are
added to 2 cm3 of the unknown solution (to be tested
for containing starch) and the mixture is gently
shaken. A DEEP BLUE-BLACK color is a positive
result (starch is present).
To test for glucose (a reducing sugar), 2 cm3 of
Benedict’s reagent are added to 2 cm3 of the
unknown solution and the mixture is heated in a
boiling water bath for 2-3 minutes. An
ORANGE/BRICK-RED color is a positive result.
(glucose is present)

When making comparison between


different solutions – for example, to
compare the glucose content of different
wine samples – it is important to carry
out all tests under the same conditions.
For example, a series of Benedict’s tests
should be performed:

on equal volume of unknown solutions.


using equal volumes of Benedict’s solution.
with all mixtures heated to the same temperature.
for the same length of time.

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