Alkenes are unsaturated hydrocarbons that contain at least one C=C bond made up of a pi bond and a sigma bond
The general formula of alkenes is CnH2n
A pibond is formed when electrons in the adjacent p orbitals overlap above and below the carbon atoms, after a sigmabond is formed
The π bond restricts the rotation of carbon atoms
The angle and shape of a double bond is trigonal planar with an angle of 120degrees
Alkenes are more reactive than alkanes due to the high electron density of the double bond and the fact that the pi-bond is slightly easier to break
Alkenes have only London forces as intermolecular forces of attraction due to non-polar bonds
Alkenes are not soluble in water due to non-polar bonds
The complete combustion of pent-2-ene is: CH3CHCHCH2CH3 + 7(and a half)O2 → 5CO2 + 5H2O
Types of isomers that can be formed using alkenes are E/Z isomers and cis-trans isomers
An electrophile is a species that are electron pair acceptors
The most stable type of carbocation intermediate is a tertiary carbocation due to the positive inductive effect of alkyl groups
Major products will be formed from tertiary (or the most stable available) carbocations
Conditions needed for the electrophilic addition of H2O to an alkene are steam in the presence of an acid catalyst, usually phosphoric acid. This reaction is called hydration
The product of the hydration reaction is an alcohol
Conditions needed for the electrophilic addition of a hydrogen halide to an alkene are that hydrogen halide gases must be at room temperature
The reaction when a halogen is added to an alkene is called halogenation
A molecule with a non-polar bond reacts as if it is an electrophile due to the C=C double bond inducing a temporary dipole in the halogen molecule
An alkene can be converted into an alkane through hydrogenation with conditions of 150 degrees celsius and a nickel catalyst
An addition polymer is formed when many monomers are bonded together via rearrangement of bonds without the loss of any atom or molecule
Monomers are molecules that combine to form a polymer and usually have a C=C bond which breaks to leave a repeating pattern
Ways in which plastics can be disposed are landfill, combustion, electricity generation, reuse, recycle, and organic feedstock
Disadvantages of recycling include the need to sort plastics into different types, expense, labor intensiveness, and the requirement of high technology
Photodegradable polymers break down chemically using energy with wavelengths similar to light, and once the breakdown begins, it cannot be stopped
In organic feedstock, plastics are separated and broken down into small organic molecules through a series of reactions to be used in producing plastics and other industries
A disadvantage of photodegradable polymers is that they may not be exposed to sufficient light