Organic 2 Alkenes Flashcards
Bromine water test for C=C type and mechanism
Ratio
Electrophilic
Addition
One mole of alkene requires one mole of Br2 to saturate it
Acidified potassium manganate (7) test
Purple decolourises
Redox (manganate reduced and organic molecule oxidised)
Produces a diol
Alkene ➡️halogenoalkane
Reagent and conditions
Type and mechanism of reaction
Hydrogen halide
Electrophilic addition
Mechanism for alkene➡️haloalkane
Permanent dipole on HX
Curly arrow from C=C to delta + H (electrophile)
HX bond breaks by heterolytic fission
Carbocation intermediate formed
Curly arrow from - X with lone pair to the C+
Haloalkane formed
HX:C=C
1 : 1
Alkenes➡️dihaloalkanes
Reagent
Type and mechanism of reaction
Halogen
Electrophilic addition
Mechanism for alkene➡️dihaloalkane
Dipole on X-X because as it comes close to the alkene, a dipole is induced as electrons are repelled by the C=C
Curly arrow from C=C to delta positive X
Heterolytic fission of X-X bond
Carbocation intermediate
Curly arrow from -X with lone pair to C+
Dihaloalkane formed
X2. : C=C
1. : 1
Markovnikovs rule
Major product is more stable than the minor product
Carbocations with more alkyl groups are more stable because they feed electrons towards the positive charge
Tertiary carbocations therefore have greater electron inducing effect
Hydration of alkenes
Product
Conditions
Reagent
Type and mechanism of reaction
Alcohol
Steam
Concentrated phosphoric acid catalyst (H3PO4)
Addition
Markovnikovs rule reactions
Alkene+ hydrogen halide
Alkene+ steam
Alkene➡️diol
Reagent
Type and mechanism
Acidified potassium manganate
Addition reaction
Oxidises double bond
Polymers
Unreactive because they’re saturated molecules
100% atom economy
Intermolecular forces and therefore their physical properties vary depending on their side groups
Recycling polymers
Thermosetting- chipped to be reformed into new products
Thermosoftening- remoulding them into new products by melting
How to remove toxic gases due to incineration
Neutralisation
Feedstock
Some plastics can be cracked into monomers which can be used as organic feedstock to make more plastics or other chemicals
Fuels
Sustainability of polymers
- use environmentally friendly reactant molecules
- use renewable raw materials
- minimise waste
- use catalysts to keep energy use to minimum
- ensure lifespan of polymer appropriate for its use