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Chemistry Revision Session 8. Naming Alkenes Name this alkene And what about (CH 3 ) 2 CHCHCH 2 ?

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Presentation on theme: "Chemistry Revision Session 8. Naming Alkenes Name this alkene And what about (CH 3 ) 2 CHCHCH 2 ?"— Presentation transcript:

1 Chemistry Revision Session 8

2 Naming Alkenes Name this alkene And what about (CH 3 ) 2 CHCHCH 2 ?

3 Isomerism What type of isomerism is this? Why does it occur?

4 Mechanisms! Explain how bromine reacts with ethene (4 marks) Identify the mechanism type!

5 Polymers Draw a section of polymer chain to show the structure of poly(propene) Draw a section of the polymer chain obtained from the monomer 1-chloroprop-1-ene! Identify the intermolecular forces present in each polymer Which would be more flexible? Why?

6 More on IMF Why does H 2 O have a higher boiling point than H 2 S? Include a diagram in your answer for water!! What is the shape of H 2 S?

7 Test! How can I differentiate between ethane and hex-3-ene in the laboratory?

8 Sorry Couldn’t resist ONE trick question- in the lab ethene will be a gas, where as, of course, hex-3-ene is a liquid. The more sensible question to ask is how to differentiate between hex-3-ene and hexane! Add bromine water- which will be decolourised by hex-3-ene (orange  colourless)

9 Definitions Explain the difference between thermosetting and thermoplastic ploymers What is a co-polymer What is the difference between a crystalline and a amorphous region of a polymer How will this affect its properties?

10 Manipulating polymers Explain how each of the following will affect a polymers strength- Adding a side group to the monomer- eg CH 3 Increasing the chain length of the polymer Substituting a Cl atom for an H atom in the monomer Substituting that Cl for an amine group

11 Manipulating Polymers Give 2 other ways I can increase the strength of a polymer Again- boring though it may be- justify your answer!

12 Manipulating polynmers Cross-linking Increasing stereo-regularity

13 Alcohols

14 Which is/are secondary alcohols and which is/are tertiary alcohols? Name the product if I oxidise- Name the functional group State the reagents and conditions

15 How would it be different if I oxidised ethanol using mild conditions? And if I spent too long drinking coffee (surely not) and came back too late I would have made which compound?

16 Dissolving Polymers The polymer with the repeating unit shown below dissolves well in water. Why? H OH ----C—C------ H H n

17 Final definitions Define the terms:- Elimination Electrophile


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