Ch13 Hydrocarbons- alkane Flashcards
5 Fuel properties
- have high energy output
- be either abundant or manufactured easily
- be easy to transport and store
- be easy to ignite
- cause minimum environmental damage
Saturated compound
a molecules in which all the atoms are linked together by single sigma bonds only
hydrocarbon
compound that contains hydrogen and carbon only
Trend in boiling point of alkane
Increases as Mr gets larger
- increased chain length and therefore increased electrons present
- more London dispersion forces so more energy required to overcome them
Trend in boiling point as branching increases
decreases as degree of branching increases
- less branched can pack together more tightly so have increased surface contact
- creates more London dispersion forces
- more energy is needed to overcome intermolecular forces
solubility of alkanes
insoluble in polar solvents
- low polarity so don’t mix with polar molecules
dissolve readily in each other as molecules link through induced dipole-dipole interactions
Alkanes chemical properties
unreactive
- CH bonds have low polarity
- single bonds linking CH are relatively strong
Combustion of alkanes in excess of oxygen
produces carbon dioxide and water
Combustion of alkanes in limited supply of oxygen
produces carbon monoxide/carbon and water
Carbon monoxide
poisonous - restricts effectiveness of blood to transport oxygen to body as binds with haemoglobin
Carbon
Soot- global dimming
Radical
particle that has at least one unpaired electron
highly reactive
substitution reaction
an atom(or group) is replaced by another atom
Conditions of radical substitution
ultraviolet radiation
Steps in radical substitution
- initiation - starts reaction by forming a radical
- propagation- maintains reaction by forming one of the products a new radical
- termination - ends reaction by removing the radicals and forming molecules