Alkene
Alkenes are hydrocarbons that have double bonds between carbon atoms and therefore are called unsaturated substance. The generic formula is CnH2n. The simplest alkene is ethene (also known as ethylene): Physical properties
Chemical properties Alkenes are relatively stable compounds, but are more reactive than alkanes. Obtainment of alkene Mainly by cracking reaction of an alkane. alkane → light alkane + alkene Hydrogenation reaction This reaction is done under a pressure of about 50 atm. We use a catalyst called Raney's nickel[?] who is an alloy of nickel and aluminium. here is an example with ethylene : CH2=CH2 + H2 → CH3-CH3 Halogenation reaction In the case of alkene, halogenation is an addition reaction. CH2=CH2 + Cl2 → ClCH2-CH2Cl Hydrohalogenation reaction It's also a reaction of addition, an electrophilic addition.
δ+ δ- δ+ δ-CH3-CH=CH2 + H-Cl → CH3-CH-CH3 |
Cl
This is an electrophilic addition with formation of a carbocation. The attacker is the H+, he will search for a source of electrons, the ones from the pi-bonding.
δ+ δ-CH3-CH=CH2 + H+ → CH3-CH+-CH3
This is also an electrophilic addition. CH3-CH+-CH3 + Cl- → CH3-CH-CH3 |
Cl
Polymerisation here is the case of the ethylene
Under a thermic source of energy, peroxide will decompose into two free radicals. RO - OR → 2 RO*
the alone electron of the RO* will bond with an electron from the pi-bonding. RO* + CH2=CH2 → ROCH2-CH2*
There is the addition of n monomers to obtain a polymer. ROCH2-CH2* + n CH2=CH2 → RO(CH2-CH2)n-CH2-CH2*
Recombinaison of two free radicals. R* + *R → R-R Oxydation reactions : ozonolysis reaction Oxydation reactions : arranged oxydation Oxydation reactions : brutal oxydation
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