Alkenes Flashcards
Why is there no rotation around a C=C bond?
- The Pi bond is formed by overlap of P orbitals
- if there was any rotation, the P orbitals would no longer overlap + the Pi bond would break
For electrophilic addition by H-Br, what is the:
- Reagent
- Type of product
- HCl, HBr <—- Hydrogen Halide
- Haloalkane
Electrophilic addition with Ethene to bromoethane?
Explain why 2-bromopropane is the major product compared to 1-bromopropane?
- 2-bromopropane is made from a secondary carbocation
- 1-bromopropane is made from a primary carbocation
- Secondary carbocations are more stable than primary due to the positive inductive effect of the 2 alkyl groups
For electrophilic addition by Br2, what is the:
- Reagent
- Type of product
- Cl2, Br2 (Halogen)
- Haloalkane (Dihaloalkane)
Electrophilic addition with Ethene through Br2?
Explain why bromine molecules react with the double bonds in alkenes?
- C=C bond is electron rich and induces a dipole in the Br2
- Partially +ve Br is attracted to the C=C bond
- Reagent used to test for alkenes
- Observation when alkenes present
- Observation when alkene not present
- Br2
- Orange to colourless
- No visible change
Structural formula for H2SO4 for electrophilic addition?
For electrophilic addition by sulphuric acid, what is the:
- Reagent
- Type of product
- H2SO4
- Alkyl hydrogen sulfate
Electrophilic addition with ethene through sulphuric acid?
For electrophilic addition by direct hydration, what is the:
- Reagent
- Conditions
- Type of product
- H2O
- Concentrated H3PO4 catalyst
- Alcohol
Electrophilic addition with ethene through direct hydration?
Write equation for the formation of an addition polymer from ethene?
Explain the difference between structural isomerism and stereoisomerism. Use examples to show how compounds with molecular formula C4H8 exhibit stereoisomerism and 3 types of structural isomerism?
Structural isomers - Molecules with same molecular formula but different structure
Stereoisomers - Molecules with same structural formula but different arrangement of atoms in space
Stereoisomers
2a lack of rotation around C=C
2b structures of E- and Z-but-2-ene
2c correct identity of E and Z isomers
Structural isomers
3a different C chain, e.g. methylpropene & but-1-ene / but-2-ene
3b different position of functional group e.g. but-1-ene & but-2-ene
3c different functional group, e.g. cyclobutane & but-1-ene / but-2-ene / methylpropene