Topic 6(B&C): Alkanes & Alkenes Flashcards
During cracking why are a variety of Alkenes & Alkanes formed with different chain lengths?
• C-C bond can break anywhere
Fractional Distillation
- Crude oil is heated in a furnace which turns most of it into vapour
- Near the top is where the shorter chain molecules condense
- Near the bottom is where longer molecules are as they have a higher melting point
- Different columns have different temperatures where different length carbon chains condense
Cracking
- Converts longer chain Hydrocarbons into smaller ones
- Heated with a ZEOLITE catalyst
Reforming
conversion of straight-chain hydrocarbons into branched-chain and cyclic hydrocarbons for EFFICIENT COMBUSTION
What pollutants are there from unburned combustion?
- Oxides of sulfur (SO2&SO3) (can cause acid rain)
- Oxides of nitrogen (NO&NO2) (can cause Acid rain)
- CO
- Unburned carbon (soot)
Catalytic converter : outline the stages of how NO & CO react in a catalytic convertor
- CO & NO are absorbed onto the surface of the catalyst
- The catalyst weakens the bonds so CO2 and N2 can be made
- Products desorbs from the surface
Hydrogenation (manufacture of margarine)
- Converts alkenes into alkanes
- Addition of Hydrogen (H2)
- Needs a Nickel catalyst
Halogenation
•Involves the addition of a halogen
Addition reaction
•Two molecules combine to form one molecule
What do Curly arrows represent?
•Movement of electron pairs
Electrophile
• Species that is attracted to a region of HIGH electron density
Electrophilic addition (define addition and define what is attacking it)
- Two molecules form one molecule
* The attacking molecule is an electrophile
Heterolytic fission
Breaking of a covalent bond so that both bonding electrons are taken by one atom forming ions ( the more electronegative one)
Carbocation
A positive ion in which the charge is shown on the carbon atom
What is a major product?
The most stable product (most R groups attached)