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What is a saturated compound?
A compound in which all of the bonds between carbon atoms are single bonds
What molecules do halogenoalkanes contain?
Carbon, Hydrogen and one or more halogen atoms
Why are the molecules in a halogenoalkane polarised?
There is a large electronegativity difference between halogens and carbon
What influences the strength of intermolecular forces of attraction in a halogenoalkane?
Molar mass and polarity
What intermolecular forces of attraction are found in a halogenoalkane?
Permanent dipole-permanent dipole attraction and van der Waals
Why do intermolecular forces become stronger down the homologous series?
Increase in molecular mass and size
Why does the boiling point of halogenoalkanes increase down the homologous series?
Increase in van der Waals forces with increase of molar mass
Why does boiling point decrease with branching?
The molecule becomes more spherical and there are less van der Waals forces between the separate molecules
What is organic synthesis?
The process of making pure organic compounds from the starting materials
What is reflux?
The repeated boiling and condensing of a reaction mixture
What is a nucleophile?
An ion or molecule (with a lone pair of electrons) that attacks regions of low electron density
What is a hydrolysis reaction?
The breaking up of molecules by reaction with water
How is hydrolysis carried out?
Heating under reflux
What do halogenoalkanes form with an aqueous alkali?
The corresponding alcohol
What do halogenoalkanes form with ammonia?
The corresponding amine
What do halogenoalkanes form with potassium cyanide?
The corresponding nitrile
What is the significance of the hydrolysis reaction?
It extends the carbon chain by one carbon
What is the reaction of primary halogenoalkanes known as?
An SN2 reaction
What is the reaction of a tertiary halogenoalkane known as?
An SN1 reaction
How does bond enthalpy affect rate of hydrolysis?
The weaker the bond (the lower the bond enthalpy) the faster the hydrolysis reaction will occur
What is an elimination reaction?
Removal of a small molecule from a larger one
Why were CFCs originally used in aerosols?
They have a low reactivity, they're volatile and they're non-toxic
Why are CFCs nonreactive and volatile?
They have strong covalent C-H bonds and no double/triple bonds as well as only weak intermolecular forces of attraction which are easily broken
Why were CFCs banned?
They cause damage to the ozone layer
How do CFC's damage the ozone layer?
Their lack of reactivity allows them to reach the stratosphere without being broken down. They are then broken down by UV radiation, causing them to form chlorine free radicles which attack the O3 molecules, converting them to O2, reducing the ozone layer