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Bromine Water
AIM: To determine the difference between the reactivity of alkanes and alkenes.
MATERIALS:
Bromine water
Pure cyclohexane
Pure cyclohexene
Molecular model kits
Test tubes
Measuring cylinders
Beakers
DISPOSAL: Place in an organic waste bottle, rinse the test tube and place rinse in an
organic waste bottle
RISK ASSESSMENT:
Chemical
Bromine Water
Risk
Not Hazardous according to Worksafe
Critieria, should not be ingested
Cyclohexane
Cyclohexene
Management
Use eye and skin protection
Use in a fume cupboard and
eye skin protection or use
in small amounts in a well
ventilated area
Use in a fume cupboard and
eye skin protection or use
in small amounts in a well
ventilated area
METHOD:
1. Place 3mL of Br water into 2 test tubes.
2. To one of the tubes add 3 drops of cyclohexane and shake the tube by flicking it
briskly.
3. To the other tube, add 3 drops of cyclohexane and shake the tube by flicking it
briskly.
4. Draw to diagram to illustrate observations.
5. Construct a model of cyclohexane and cyclohexene molecule, with a model kit.
VARIABLES:
o
Controlled variables:
1
Amount of Br water
Amount of Cyclohexane
Amount of Cyclohexene
Concentration of Br water
Temperature of surroundings
Air Pressure
Humidity of surroundings
Method of mixing chemicals (Flicking 3 times)
Dependent variable:
The amount of Br water required
Independent variable:
The alkane and alkenes
IMPROVING VALIDITY:
Repetition
Using a range of different Alkanes and Alkenes
IMPROVING RELIABILITY:
Repetition
Improving measurements
o Using a pipette to measure out the amount of bromine water, rather then a
measuring cylinder
RESULTS:
Bromine Water
Cyclohexane w/BW
Cyclohexene w/BW
DISCUSSION: Alkenes are more reactive than alkanes due to the presence of their double
bond. Alkenes go through what is called an addition reaction. It is where in an alkene; a
double bond is broken and replaced with two new covalent bonds added across double bond
where a foreign element/compound attaches itself.
2
1, 2 dibromoethane
As mentioned above this is described as an addition reaction because extra elements are
being added to the hydrocarbon and breaking the double bond. Alkanes go through a process
called a substitution reaction. The substitution needs the presence of UV light to go
through. An example is shown below:
E.g.
H
H
I
I
H C C H + Cl2
I
I
H
H
H Cl
UV
I
I
H C C H + HCl
I
I
H H
When for example Ethane and Bromine undergo a substitution reaction the compound HBr is
formed. This is due to one of the Br being substituted with an H on the hydrocarbon.
Therefore Br2 is broken into two, one atom goes and joins the hydrocarbon and the H which
the Br replaces attaches on to the free Br to make HBr.
CONCLUSION: Alkenes are more reactive than alkanes as seen in the results of this
experiment due to the presence of their double bond.