properties of hydrocarbons

Properties of Hydrocarbons

Physical Properties of Alkanes

Non polar compounds Insoluble in water Less dense than water and so will float on top

of the water Dissolve in organic solvents (eg dry cleaning

fluid) and in each other (eg Petrol is a mixture of alkanes)

Low melting and boiling points

Chemical Properties of Alkanes

Very unreactive Don’t react with concentrated sulfuric acid or

concentrated bases Don’t react with strong oxidants (dichromate or

permanganate ions) Will react with bromine but only if heated or in

strong sunlight

Substitution Reactions

Where an atom or group of atoms is displaced by an atom or group of atoms

CH4 + Br2 → CH3Br + HBr Non specific reaction. Can not control which

hydrogen is substituted or how many are substituted

CH3Br + Br2 → CH2Br2 + HBr

Substitution reactions Very slow with heat or sunlight Product is a mixture of bromoalkanes Products would need to be separated by

fractional distillation giving only a very small yield of each

Combustion of Alkanes

Very useful group as fuels Fuels burn completely when there is sufficient

oxygen, forming CO2 and H2O If oxygen is limited then incomplete

combustion occurs and carbon (soot) and carbon monoxide (CO) are formed as well as CO2 & H2O

Combustion of Alkanes Incomplete combustion is less efficient and so

produces less energy per mole that complete combustion

Balancing Combustion Equations

Write correct formula Alkane + O2 → CO2 + H2O

Balance carbon Balance hydrogen Balance oxygen (Fractional coefficients are

acceptable in combustion equations)

Physical Properties of Alkenes

Non polar molecules so they are insoluble in water

Less dense than H2O, so floats on water Low melting and boiling points

Chemical Properties of Alkenes

Combustion is incomplete in air but will burn completely in pure O2

Burn with a smoky flame in air due to unburnt carbon. Higher carbon to hydrogen ratio means some carbon remains unburnt

More reactive than alkanes because the can undergo addition and oxidation reactions

Addition Reactions The colour of bromine rapidly disappears when

shaken with an alkene C2H4 + Br2 → C2H4Br2

The reaction site is the alkene double bond. One bromine adds to the carbon on one end of the double bond and the other bromine to the other end. The double bond becomes a single bond

Addition Reactions

C

H

H

C

H

H

C

H

H

C

H

H

+

Br Br

Br Br

C

H

H

Br C

H

H

Br

C

H

H

Br C

H

H

Br

1,2 dibromo ethane

Addition Reactions An alkene can be converted to the

corresponding alkane by the addition of hydrogen gas

The reaction conditions for this to occur are heat, high pressure and a nickel catalyst

This reaction is called catalytic hydrogenation

Addition Reactions

C

H

H

H C

H

C H

H

C

H

H

H C

H

C H

H

+

H H

H H

Ni Cat HEAT PRESSURENi Cat

Ni Cat

HEAT PRESSURE

HEAT PRESSURE

C

H

H

H C

H

H

C

H

H

H

C

H

H

H C

H

H

C

H

H

H

This reaction is used to turn a pourable oil into a spreadable fat (margarine)

Other Addition Reactions

Alcohols can also be made from alkenes by the addition of water in the presence of an acid catalyst (conc. Sulfuric acid)

C

H

H

C

H

H

C

H

H

C

H

H

+

H O H

H O H

H+ CatH+ Cat

H+ Cat

C

H

H

H C

H

H

O H

C

H

H

H C

H

H

O H

Other Addition Reactions

Alkenes can add to each other to form polymers (very large molecules)

C

H

H

C

H

H

C

H

H

C

H

H

CatCat

Cat

C

H

H

H C

H

H

C

H

H

C

H

H

C

H

H

C

H

H

C

H

H

C

H

H

C

H

H

C

H

H

.

C

H

H

H C

H

H

C

H

H

C

H

H

C

H

H

C

H

H

C

H

H

C

H

H

C

H

H

C

H

H

.

ethene polyethylene