BioWorkbook1A Ans e
BioWorkbook1A Ans e
Book 1A
p.1/38
(Answer varies with Ss. The recommended quantity of jelly powder and water is stated
on the packet of the jelly powder. Jelly will not set if it is too dilute.)
Method II. This makes sure the concentrations of the jelly solutions in different
containers are the same.
A Identifying variables
Independent
variable
(What will you
change?)
Dependent variable
(What will you
measure?)
Controlled
variables
(What will you keep
constant?)
The amount of jelly
solution in each
container, the size
and shape of the
containers, the
cooling temperature,
the time allowed for
setting, etc.
Control
(What is the control
in this experiment?)
The jelly without
fresh pineapple.
Book 1A
p.2/38
C Collecting data
1
During the preparation of jelly solution, the hot water may burn our body.
The knife used to cut the pineapple is very sharp and may cut our fingers.
2 glass rods
1 refrigerator
1 knife
2 beakers (500 cm )
fresh pineapple
hot water
2 plastic containers
jelly powder
Procedure
Book 1A
p.3/38
Add 50 g of jelly powder and 200 cm3 of hot water to a beaker. Stir the mixture with a
glass rod until all the jelly powders dissolve.
Pour 100 cm3 of jelly solution into two containers respectively. Leave the jelly solutions
at room temperature for one hour.
Put the small pieces of fresh pineapple into one of the containers. Then, refrigerate two
containers overnight.
Observe any changes of jelly solutions in the two containers on the next day.
Results
The jelly without fresh pineapple set.
The jelly with fresh pineapple does not set.
Analysis and discussion
1
2
It is used to confirm that the presence of fresh pineapple is the only factor that prevents
the jelly from setting.
(Answer varies with the design.)
Conclusion
Book 1A
p.4/38
To allow entry of a suitable amount of light. A dim image may result if there is
insufficient light while a faint image may result if the light is too bright.
The coarse adjustment knob leads to a larger degree of movement of the body tube.
Any downward movement of the body tube controlled by the coarse adjustment knob
may damage the objective or the slide because the distance between the objective and the
slide is very small.
Book 1A
p.5/38
3
Area of specimen
observed (small / large)
Details of specimen
(more / less)
Brightness of image
(bright / dim)
4
Low power
large
High power
small
less
more
bright
dim
Towards the left. An inverted image is formed in the microscope. It moves in a direction
opposite to the actual movement of the flatworm.
Practical 2.2
Practical 2.3
Book 1A
p.6/38
No. Not all of them contain chloroplasts or chlorophyll. Only those with chloroplasts are
green.
Differences:
1
Plant cells have a definite shape while the animal cells do not.
Plant cells have a thick cell wall and some have chloroplasts. Animal cells do not
have cell walls or chloroplasts.
Plant cells usually have a large vacuole while animal cells do not.
Book 1A
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Practical 2.4
Book 1A
p.8/38
Eukaryotic cell
Usually larger
Absent
Present
Absent
Present
Absent
Present
Size
Genetic material
Nuclear membrane
Organelles bounded
by a double membrane
(e.g. mitochondria)
Endoplasmic reticulum
14 cm
= 0.00023 cm = 2.3 m
60 000
13 cm
= 0.00104 cm = 10.4 m
12 500
Book 1A
p.9/38
Experimental
Rises
Control
Sucrose solution on the outside of the tubing will affect the result. Rinsing the tubing
ensures no such sucrose solution is present.
Osmosis.
Differential permeability.
After a certain period of time, the force produced by the weight of the liquid column
balances the force developed by the water potential gradient.
The liquid level will drop and the tubing will eventually shrink.
Practical 3.2
Rises
Book 1A
p.10/38
Set-up B is a control. It shows that any change in liquid level in set-up A is due to the
concentrated sucrose solution.
Distilled water has a higher water potential than concentrated sucrose solution, so there
is a net movement of water from the distilled water to concentrated sucrose solution
through the differentially permeable animal tissues by osmosis. The volume of liquid
inside the thistle funnel increases and the liquid level rises.
Practical 3.3
0.45%
0.9%
1.35%
1.8%
0% and 0.45% sodium chloride solutions are hypotonic to the red blood cells. At these
concentrations, the red blood cells swell and burst. It shows that the water potential of
the red blood cells is lower than that of the sodium chloride solution. Water enters the red
blood cells by osmosis.
Book 1A
p.11/38
1.35% and 1.8% sodium chloride solutions are hypertonic to the red blood cells. At these
concentrations, the red blood cells shrink and become wrinkled. It shows that the water
potential of the red blood cells is higher than that of the sodium chloride solution. Water
leaves the red blood cells by osmosis.
Practical 3.4
In less concentrated
sucrose solution
The cytoplasm swells up gradually until the cell membrane presses tightly against the
cell wall.
Book 1A
p.12/38
Book 1A
p.13/38
No. This is because the concentration of the content / water potential of each cell varies.
Practical 3.5
3.10
Percentage
change in
weight (%)
11.11%
Average
Distilled
Water
10%
sucrose
solution
2.76
2.87
2.83
2.82
2.79
2.80
2.81
2.80
-0.71%
20%
sucrose
solution
2.84
2.83
2.85
2.84
2.57
2.62
2.55
2.58
-9.15%
To prevent the evaporation of water which may change the concentration of the liquids in
the set-ups and affect the results.
To absorb the surplus water on the surface of the potato strips which may increase the
weight of the potato strips and affect the results.
To minimize the water loss from the potato strips by evaporation. Any water loss will
decrease the weight of the potato strips and affect the results.
Book 1A
p.14/38
The potato strips in distilled water become heavier. This is because the water potential of
distilled water is higher than that of the potato cells. Water enters the potato strips by
osmosis.
The weight of the potato strips in 10% sucrose solution changes very slightly. This is
because the water potential of 10% sucrose solution is nearly the same as that of the
potato cells. There is almost no net movement of water into or out of the potato strips.
The potato strips in 20% sucrose solution become lighter. This is because the water
potential of 20% sucrose solution is lower than that of the potato cells. Water leaves the
potato strips by osmosis.
Living plant tissues are differentially permeable. When living plant tissues are placed in
solutions with different water potential, osmosis takes place.
Practical 3.6
Book 1A
p.15/38
the nutrition of some single-celled organisms, e.g. Amoeba engulfs food particles by
phagocytosis;
body defence against diseases, e.g. in humans and other mammals, certain white
blood cells engulf harmful microorganisms by phagocytosis.
Book 1A
p.16/38
Grinding action produces heat. The high temperature resulted may denature any enzyme
present in the tissues.
It is a control to show that no oxygen is given off from the liver extract.
It is a control to show that no oxygen is given off from the hydrogen peroxide.
No. This experiment only shows that the breakdown of hydrogen peroxide is speeded up
by the liver extract. Boiled liver extract, instead of fresh liver extract, can be used in a
further experiment. If boiled liver extract has no catalytic action, it is more likely that the
reaction is catalysed by an enzyme.
Yes. For the three test tubes, only one variable (the sample) is changed at a time, other
variables (e.g. the volume and temperature of hydrogen peroxide, liver extract and
distilled water) are kept constant.
The breakdown of hydrogen peroxide is catalysed by the liver extract, probably by an enzyme
in the liver tissues. Nevertheless, further experiments should be done to confirm this.
Book 1A
p.17/38
Practical 4.2
Book 1A
p.18/38
20
40
60
80
100
To ensure that the amylase and starch solutions inside the tubes reach the respective
temperatures before the reaction starts.
To prevent the changing of the condition of a mixture by any residue in the dropper.
Amylase is inactive at low temperatures. Its activity increases with temperature and is
the highest at 60C. Afterwards the activity decreases and stops at 100C. With a rise in
temperature, the kinetic energy of amylase and starch molecules increases. They collide
and react more frequently. As the temperature increases further, the active sites of
amylase become distorted (i.e. the enzyme is denatured) and the reaction rate decreases.
At 100C, all amylase is denatured and no reaction takes place.
Starch will be digested and blue-black colour will disappear. This is because the
inactive amylase will resume its activity with an increase in temperature.
Starch will not be digested and blue-black colour will remain. This is because the
activity of the denatured amylase will not restore even when it is cooled.
Amylase is inactive at low temperatures. Its activity increases with temperature until it
reaches a maximum. Afterwards the activity decreases and stops.
Practical 4.3
Book 1A
p.19/38
pH
3.2
4.0
5.2
6.0
7.0
8.0
To ensure the invertase has sufficient time to catalyse the breakdown of sucrose into
glucose and fructose.
Weighing the precipitate formed. / Using an arbitrary system of + to denote the relative
amount of precipitate.
Invertase is most active in the acidic medium (pH 5.2) and less active in the neutral and
alkaline medium.
Practical 4.4
Book 1A
p.20/38
Results
Tube
(p. 4-13)
Sample that
contains
copper(II) sulphate
solution
silver nitrate solution
distilled water
Questions
(p. 4-14)
It is a control to show that the activity of invertase is slowed down or stopped by the
inhibitor.
No or less brick-red precipitate is formed in tubes A and B because copper(II) ions and
silver ions are inhibitors of invertase. They slow down or stop the activity of invertase.
Brick-red precipitate is formed in tube C because the activity of invertase is not affected
by any inhibitor.
Conclusion
(p. 4-14)
Copper(II) ions and silver ions are inhibitors of invertase. They slow down or stop the activity
of invertase.
Practical 4.5
Book 1A
p.21/38
Results
Well
(p. 4-17)
Sample
Pineapple juice
Papaya juice
Guava juice
Distilled water
Questions
(p. 4-17)
It is a control to show that the formation of the clear zones is due to the fruit juices.
Proteases in the fruit juices break down the white milk protein nearby. Therefore, the
white colour of the milk disappears and the clear colour of the agar is shown around the
wells containing fruit juices.
It is because the proteases in pineapple are denatured by the high temperature during the
canning process.
The proteases in fresh pineapple can break down the proteins in beef steak. Leaving beef
steak in contact with slices of pineapple for half an hour allows enough time for the
enzymes to work.
Conclusion
(p. 4-18)
Pineapple, kiwi fruit, papaya and guava contain proteases that can break down proteins, but
their activities differ from one another.
Practical 4.6
Book 1A
p.22/38
(p. 4-20)
Protease. / Lipase.
(Answer varies with Ss. The recommended quantity of washing powder and water is
stated on the packet of the washing powder. This ensures the washing powder works in
the best conditions.)
A Identifying variables
Independent variable
(What will you change?)
The brand of the washing
powder.
Dependent variable
(What will you measure?)
Controlled variables
(What will you keep
constant?)
C Collecting data
1
Book 1A
p.23/38
Book 1A
p.24/38
(p. 4-22)
Objective
(Answer varies with Ss.)
Apparatus and materials
(Answer varies with Ss.)
Procedure
Ss can carry out the experiment in a number of ways.
Ss may conduct the experiment by using a milk-agar plate (see Practical 4.5).
Another method is using two test tubes containing equal volumes of boiled egg white cubes.
Add the two washing powder solutions into the test tubes and compare the rate of dissolving
of the egg white cubes.
Results
(Answer varies with Ss.)
Analysis and discussion
1
It is because proteins in silk and wool will be broken down by the proteases.
Conclusion
Book 1A
p.25/38
(p. 5-5)
Clinistix paper
Glucose solution
Original colour
Pink
Final colour
Purple
Pink
Pink
Distilled water
Glucose solution
Distilled water
No observable change
Iodine solution
Original colour
Brown
Final colour
Blue-black
Brown
Brown
Distilled water
Before immersing
into organic solvent
Yes
Yes
Yes
Distilled water
No
Not applicable
Cooking oil
Book 1A
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Book 1A
p.27/38
Albustix paper
Original colour
Final colour
Yellow
Blue-green
Distilled water
Yellow
Yellow
DCPIP solution
Original colour
Final colour
Vitamin C solution
Blue
Colourless
Blue
Blue
Distilled water
Blue
Blue
Questions
(p. 5-6)
No. This is because these food tests are qualitative tests for showing the presence of
certain food substances. They are not quantitative tests.
The water bath has a better control over the temperature and can prevent bumping of the
mixture.
As the red colour of the blood will mask the results of the Benedicts test, the blood
sample should be diluted with distilled water first. Alternatively, the blood sample should
be centrifuged and the plasma collected is used for the Benedicts test.
The translucent spot caused by lipids is permanent. On the contrary, the translucent spot
caused by water disappears as water evaporates.
Lipids but not proteins dissolve in organic solvent. Thus, the translucent spot caused by
lipids disappear whereas the one caused by proteins remains on the filter paper.
Book 1A
p.28/38
Boiling destroys the reducing property of vitamin C. Thus, only the vitamin C
solution that has not been boiled can reduce the blue DCPIP solution and
decolourize it.
No. Glucose, like vitamin C, is reducing and will decolourize DCPIP solution no matter
vitamin C is present in the sample or not.
Practical 5.2
Results
Food
sample
(p. 5-12)
Glucose
Reducing
sugars
Starch
Lipids
Proteins
Vitamin C
Question
(p. 5-12)
Practical 5.3
(p. 5-14)
Book 1A
p.29/38
Fruits or vegetables that have juices very pale in colour. The pale colour of the juices will
not mask the decolourization of DCPIP solution.
Book 1A
p.30/38
A Identifying variables
Independent variable
(What will you change?)
The type of fruits and
vegetables.
Dependent variable
(What will you measure?)
Controlled variables
(What will you keep
constant?)
C Collecting data
1
Take any dilution factor of the juices into consideration in the comparison of vitamin C
content.
Repeat the experiment with more samples from the same types of fruits and vegetables.
The knife used to cut fruits and vegetables is very sharp and may cut our fingers.
(p. 5-16)
Objective
Book 1A
p.31/38
1 filter funnel
filter paper or fine muslin
0.02% DCPIP solution
distilled water
fruits and vegetables (e.g. orange, lemon,
cabbage)
Procedure
1
Put the small pieces into a mortar and grind with a small known quantity of cool
distilled water (if necessary) using the pestle.
Squeeze the ground materials through several layers of pre-moistened fine muslin or
filter them through a filter paper to remove the debris. Collect the juice extracted.
Skip this step if a fine and fairly colourless suspension is obtained.
Repeat steps 4 and 5 with the juices extracted from different fruits and vegetables. If the
decolourization is too quick (i.e. the juice is too concentrated), dilute the juice by a
known volume of distilled water and repeat steps 4 and 5 again. Take this dilution factor
into consideration in the comparison of vitamin C content.
Results
Sample
Lemon
Orange
Cabbage
Distilled water
Reducing property.
The vitamin C content will decrease as vitamin C will be oxidized by the air.
Book 1A
p.32/38
Fruits or vegetables that have juices very dark in colour cannot be used. The dark colour
of the juices masks the decolourization of DCPIP solution.
Conclusion
Book 1A
p.33/38
6 Nutrition in humans
Practical 6.1
Questions
(p. 6-2)
1
A
Mouth
Oesophagus
Stomach
Duodenum
Pancreas
Appendix
Ileum
Caecum
Liver
Colon
Rectum
Anus
ABCDG
JKL
3
Structure
Ingestion, digestion
Digestion
Digestion, absorption
Digestion, absorption
Egestion
Practical 6.2
Proteins.
(p. 6-4)
Book 1A
p.34/38
Book 1A
p.35/38
A Identifying variables
Independent
variable
(What will you
change?)
The solutions in the
test tubes.
Dependent variable
(What will you
measure?)
The disappearance
of egg white cubes.
Controlled
variables
(What will you keep
constant?)
Number and size of
egg white cubes,
temperature and total
volume of solution,
etc.
Control
(What is the control
in this experiment?)
A test tube with an
egg white cube,
hydrochloric acid
and distilled water. A
test tube with an egg
white cube, sodium
carbonate solution
and distilled water. A
test tube with an egg
white cube and
distilled water.
C Collecting data
1
Provide a higher temperature, use smaller egg white cubes instead of a large one, raise
the egg white cube from the bottom of the test tube by using a toothpick, etc.
The knife used to cut the hard-boiled egg is very sharp and may cut our fingers.
Dilute hydrochloric acid is corrosive and dilute sodium carbonate solution is irritant.
Handle the knife with care. Wear disposable gloves. Wash hands thoroughly with liquid
soap and water after the experiment.
(p. 6-6)
Objective
Book 1A
p.36/38
Procedure
1
Cut the egg white of the hard-boiled egg into six small cubes of length 0.5 cm and put
one in each of the six test tubes.
Test tube
Solution
3
3
A
5 cm pepsin solution + 5 cm dilute hydrochloric acid
B
5 cm3 pepsin solution + 5 cm3 dilute sodium carbonate solution
C
5 cm3 pepsin solution + 5 cm3 distilled water
D
5 cm3 hydrochloric acid + 5 cm3 distilled water
E
5 cm3 sodium carbonate solution + 5 cm3 distilled water
F
10 cm3 distilled water
3
Leave the test tubes in a water bath at 37C overnight.
4
Observe and note any changes in the size and appearance of the egg white cube in each
test tube.
Results
Test tube
A
B
C
D
E
F
Observation
The egg white cube disappears.
The egg white cube remains intact.
The egg white cube remains intact.
The egg white cube remains intact.
The egg white cube remains intact.
The egg white cube remains intact.
Stomach.
Protease.
Peptides.
Positive. Pepsin is a protein and it changes the colour of the Albustix paper.
Conclusion
Practical 6.3
Results
Book 1A
p.37/38
(p. 6-10)
Mixture of oil and bile salt
solution
An emulsion is formed.
Appearance
Question
(p. 6-10)
Water cannot break down oil into small droplets as the bile salt solution does. Therefore, no
emulsion is formed and two layers of liquids can be seen.
Conclusion
(p. 6-10)
Bile salts can break down lipids into small droplets. It is an emulsifying agent.
Practical 6.4
Reducing sugars
At start
Less water allows a higher concentration of starch or reducing sugar molecules for easy
detection.
Book 1A
p.38/38
3
Part of the model
Dialysis tubing
Blood
Starch and amylase mixture in Mixture of undigested food and digestive enzymes in the
the tubing
small intestine
4
Amylase digests starch into maltose. Maltose molecules are small enough to pass
through the tubing and diffuse into the water outside the tubing, whereas the large
starch molecules are retained inside the tubing.
Through digestion, food substances are broken down into small molecules that can
diffuse through the intestinal wall / epithelium into the blood for use in our body.
Maltose molecules are not small enough to pass through the small intestine.
The small intestine can absorb digested food by active transport but the dialysis tubing
cannot.
The small intestine can secrete enzymes but the model cannot.
The small intestine shows peristalsis but the model does not.
There are many types of food molecules in the small intestine apart from starch.
The food molecules have to pass through more than one layer of cells instead of only one
layer of tubing.
The blood is enclosed in blood vessels.
Diffusion rate of the reducing sugar molecules can be increased by stirring the
surrounding water and using a water bath at a higher temperature.
More concentrated solutions of starch and amylase can be used to speed up the reaction
rate.