alkenes Flashcards
what shape do alkenes have
trigonal planar (120 bond angle)
what is a single bond and a double bond composed of
C−C single bond σ
C=C double bond σ and π
Why is there no rotation around a C=C double bond?
because too much energy is required to rotate the double bond
how are alkenes EZ isomers
because of the lack of rotation around the C=C bond
what is an electrophile
An electron-pair acceptor
what are the 3 types of electrophiles
· Hydrogen halides H-Cl H-Br H-I
· Halogens Cl-Cl Br-Br
· Sulphuric acid H-OSO3H
give the reagent and product from Electrophilic Addition with Hydrogen Halides
· Reagent: HCl, HBr
· Type of product: Haloalkane
What are alkyl groups?
Methyl (CH3), ethyl (CH2CH3), propyl (CH2CH2CH3) etc.
an alkane missing one hydrogen.
What is a positive inductive effect?
The ability to release electron density through a covalent bond
Why are tertiary carbocations more stable than primary carbocations?
tertiary carbocations have 3 alkyl groups bonded to a positive carbon whereas primary has only 1. There is a greater positive inductive effect from three alkyl groups in 3° carbocations compared to two alkyl groups in 2° carbocations
in what types of alkenes do major and minor products form
only in asymmetrical
Explain why 2-bromo propane is the major product when propene reacts with Hbr
· 2-bromopropane is made from a secondary carbocation
· 1-bromopropane is made from a primary carbocation
· Secondary carbocations are more stable than primary carbocations due to the positive inductive effect of the two alkyl groups (compared to one)
give the reagent and product from Electrophilic Addition with Halogens
· Reagent: Cl2, Br2
· Type of product: Haloalkane
Bromine reacts with alkenes, even though bromine is a non-polar molecule. Explain why bromine molecules react with the double bonds in alkenes.
· The C=C bond is electron rich
· and induces a dipole in the Br2
· δ+ Br attracted to C=C double bond
what is the chemical test for alkenes. give observations when alkene is present and not present
· Reagent used to test for alkenes: Br2 (bromine liquid)
· Observation when alkene present: Orange to colourless
· Observation when alkene not present: No visible change
give the reagent and product from Electrophilic Addition with Sulphuric Acid
· Reagent: H2SO4
· Type of product: Alkyl hydrogen sulphate
describe the 3 step process to make alcohols from alkenes
Step 1
· alkene + H2SO4 → alkyl hydrogen sulphate
Step 2
· alkyl hydrogen sulphate + H2O → alcohol + H2SO4
Role of the H2SO4 in the two-step transition from alkene to alcohol
· H2SO4 is reproduced (reformed) so it is a catalyst
give the reagents conditions and product formed from direct hydration
· Reagent: H2O
· Conditions: Conc. H3PO4 catalyst / conc H2SO4
· Type of product: Alcohol
how is an addition polymer formed
long chain made from lots of monomers (alkenes)
why does PVC tend to be hard ad rigid
bc there are permanent dipole dipole forces between chains due to delta + c and delta - cl
what does adding plasticisers to PVC’s do
reduce the effectiveness of attractions and makes plastic more flexible
why are most plastics non- biodegradable
due to the strong covalent bonds present between the atoms in the polymer molecules