Save
Chemistry
Hydrocarbons 2.5
Save
Share
Learn
Content
Leaderboard
Share
Learn
Created by
Christian Villaruz
Visit profile
Cards (14)
Compounds derived from organisms that lived long ago that can be used as a source of energy
Fossil fuels
View source
Combustion of fossil fuels
Produces
CO2
- a
greenhouse
gas that causes an increase in the Earth's
temperature
View source
Insufficient oxygen during combustion of fossil fuels
Carbon monoxide
, a
toxic gas
, is formed
View source
Combustion of fossil fuels
Produces SO2 and
NOx
which react with water molecules in the air to produce H2SO4 and HNO3 -
acid rain
View source
SO2 and
NOx
also cause health problems for people with
breathing
difficulties
View source
Alkanes
Saturated
hydrocarbons with the general formula CnH2n+2, generally
unreactive
since they are non-polar and only contain sigma (σ-) covalent bonds
View source
Combustion of alkanes
1.
Alkanes
burn in excess
oxygen
to produce carbon dioxide and water
2. If
insufficient
oxygen is present, carbon
monoxide
or even carbon will form
View source
Halogenation of alkanes
1. Alkanes react with
chlorine
in UV light to form a
halogenoalkane
2. Mechanism has three stages:
initiation
,
propagation
,
termination
View source
Alkenes
Unsaturated
hydrocarbons with the general formula
CnH2n
, have at least one C=C double bond made up of a sigma (σ-) bond and a pi (π-) bond
View source
Hydrogenation of alkenes
Ethene reacts with hydrogen and a
nickel
catalyst at 150°C to produce
ethane
View source
Electrophilic addition of halogens to alkenes
1.
Halogens
react with
alkenes
to form dihalogenoalkanes
2. Mechanism involves the use of
'curly arrows'
to show the movement of a pair of
electrons
View source
Addition of hydrogen halides to alkenes
Symmetrical alkenes produce one product, unsymmetrical alkenes produce a
major
and
minor
product
View source
Addition polymerisation
The
double bonds
in
alkenes
and substituted alkenes (monomers) can open up and join together to form long chains called polymers
View source
Z isomerism
Example of stereoisomerism, where compounds have the same structural formula but a different arrangement in
space
due to the inability of the groups attached to the double-bonded carbon atoms to
rotate
View source