4.1.6/7 : Properties and reactions of alkanes Flashcards

1
Q

What is a homologous series?

A

A homologous series is a family of organic compounds with the same functional group, but each successive member differs by CH2.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What does saturated mean?

A

Only contains single bonds

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the general formula of an alkane?

A

CnH2n+2

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What is a sigma bond?

A

An overlap of molecular orbitals/electron clouds between bonding atoms.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the shape and bond angles of alkanes?

A

Every C atom has a tetrahedral shape with a bond angle of 109.5 degrees.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Why is the bond angle 109.5 degrees?

A

Carbon forms 4 covalent bonds and the pairs of electrons in the bonds all repel each other, causing them to be as far apart as possible.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Why are alkane molecules considered to be non-polar?

A

The electronegativity values of C and H are very similar (C 2.55 and H 2.20) so there are no significant dipoles.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are the type of intermolecular forces between alkane molecules and why do they occur?

A

As the electrons are always moving around the shells, there may occasionally be a lack of balance in charge distribution. This causes an instantaneous dipole, which will induce dipoles in neighbouring molecules, causing weak London forces.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Why does the boiling point of ab alkane increase as its carbon-chain length increases?

A
  • As an alkane chain gets longer, it’s relative molecular mass increases
  • Larger molecules have more surface area so more points of contact with adjacent molecules
  • This increases the number of London forces
  • so more energy is needed to overcome them ( so that the alkane can change state)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Why do compounds with more branches have lower boiling points?

A
  • Manot fit together as closely and neatly
  • so there are fewer surface area interactions between molecules
  • This means that there are fewer London forces than in straight chain isomers
  • so less energy is needed to overcome them
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the two reasons for which alkanes have low reactivity?

A
  1. All of the covalent bonds have high bond enthalpies - a large amount of energy is required to break them
  2. The C-H sigma bonds have very low polarity due to the electronegativity values of C and H being very similar. The lack of dipoles means that the molecules are less likely to attract other molecules to react with.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Why are alkanes good fuels?

A

Alkanes are good fuels as they release a large amount of energy per gram of fuel.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What type of reaction is combustion?

A

Combustion is a highly exothermic oxidation reaction.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is complete combustion?

A

Complete combustion is oxidising a fuel in a plentiful supply or air/oxygen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What kind of flame is produced by the complete and incomplete combustion of alkanes?

A

Complete - makes a clean blue flame and transfers the max. amount of thermal energy because it fully oxidises carbon and hydrogen

Incomplete - makes a cooler dirty yellow flame

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the balanced equation for the complete combustion of methane?

A

CH4 (g) + 2O2 (g) -> CO2 (g) + 2H2O (l)

17
Q

What is incomplete combustion?

A

Incomplete combustion is oxidising a fuel in a limited supply of air/oxygen

18
Q

What are the products of complete and incomplete combustion?

A

Complete - carbon dioxide and water only

Incomplete - carbon particles (soot), water, carbon dioxide, carbon monoxide (toxic gas!!)

19
Q

What are the 3 stages of the radical substitution mechanism?

A
  1. Initiation - the formation of the halogen radicals
  2. Propagation - two steps that build up the desired product in a side reaction
  3. Termination - two radicals collide and make a stable product
20
Q

What is a disadvantage of the radical substitution mechanism?

A

It is very unpredictable and difficult to control as the reactions are randomly caused by a very reactive radical colliding with another species. A mixture of products is formed, which need to be separated by processes such as fractional distillation or chromatography before they can be used.

21
Q

Show the chlorenation of methane to form chloromethane using the radical substitution mechanism

A
  1. Initiation

Cl2 -> 2Cl. (UV light/300 degrees celcius needed)

  1. Propagation

CH4 + Cl. -> .CH3 + HCl
.CH3 + Cl2 -> CH3Cl + Cl.

  1. Termination

2Cl. -> Cl2
2.CH3 -> C2H6
.CH3 + Cl. -> CH3Cl

A mixture of products is produced by random collisions between radicals. Only CH3Cl is desirable so this reaction has a low atom economy.

22
Q

What is the general formula for balancing the complete combustion of alkanes?

A

CnH2n+2 + 3n+1/2 oxygen -> n carbon dioxide + n+1 water