Chapter 12 Flashcards

1
Q

Where are alkanes found?

A

They are found in crude oil deposits as they lack reactivity.

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

How do you separate alkanes?

A

A fractional column is used in order to extract them, small molecules with lower boiling points travel to the top before they separated. Whereas the larger molecules with high boiling points are separated at the bottom.

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

What is the general formula for an alkane?

A

CnH2n+2

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

How are alkanes bonded?

A

As they are saturated they are joined to 4 other atoms by sigma bonds.

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

What is a sigma bond?

A

Sigma bond is the result of the overlap of two orbitals one from each bonding atom. Each overlapping orbital contains one electron so the Sigma bond has two electrons that are shared between the bonding atoms.

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

What is the shape of an alkane?

A

Each carbon atom is surrounded by four electron pairs with four Sigma bonds. The position result in a 3D tetrahedral arrangement around each carbon atom with a bond angle of approximately 109.5°. The sigma bond acts as axes around which the atoms can rotate freely.

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

What happens as the chain length increases?

A

The boiling point of the alkane also increases as the molecules have a larger surface area so more surface contact is possible between the molecules. The London forces will be greater so more energy is required to overcome the forces.

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

What forces are found between the molecules in an alkane.

A

As they are non polar they have London forces which are weak.

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

What does the effect of branching have on the boiling point?

A

More branching decreases the boiling point as there are fewer surface points of contact between the molecules giving fewer London forces. Additionally the branches get in the way and prevent branch manager is getting his closest straight-chain is decreasing the intermolecular forces further.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Why do alkanes lack reactivity

A

As the C-C bonds are non polar and the C-C and C-H sigma bonds are strong. The electronegativity of carbon and hydrogen are so similar that the C-H bond is considered to be non-polar.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What do alkanes produce when in a plentiful supply of oxygen during combustion?

A

Carbon dioxide and water

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What happens when there is a limited supply of oxygen during combustion?

A

It is incomplete therefore carbon monoxide or carbon can be produced.

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

For every CH2 how many extra oxygen molecules do you need?

A

1 1/2 molecules.

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

What is radical substitution?

A

It is a very reactive species. An atom or group of atoms with a unpaired electron formed by homolytic fission. It becomes a substitution reaction as the H in the alkane is replaced with another atom or group of atoms

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

What is the mechanism for the bromination of the methane?

A

Radical substitution

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

What are the three main stages of radical substitution?

A

Initiation, propagation, termination.

17
Q

What happens during the initiation stage?

A

The reaction starts when the covalent bond and the Br molecule is broken by homolytic fission. Each bromine atom takes one electron from the pair forming two highly reactive bromine radicals. The energy for this bond fission is provided by UV radiation.

18
Q

What happens during propagation?

A

The reaction propagate through to steps, a chain reaction they both have radicals on each side. In the first propagation step a bromine radical reacts with a
C – H bond and methane forming a methyl radical and a molecule of hydrogen bromide. In the second propagation step each metre radical reacts with another bromine molecule forming the organic product bromoethane and a new bromine radical.

19
Q

What energy is required in order to provide initial energy for a reaction to take place?

A

UV radiation

20
Q

What happens without any UV radiation?

A

No reaction will occur therefore bromine will stay red (no colour change)

21
Q

What is carbon monoxide?

A

It is a colourless odourless and highly toxic gas.

22
Q

Why is carbon monoxide deadly?

A

It binds to haemoglobin which prevents haemoglobin from transporting oxygen to respiring cells. This can be carboxyhaemoglobin.

23
Q

How is propagation terminated?

A

When two radicals collide.

24
Q

What happens in termination?

A

It is when the two radicals collide together for me a molecule with all electron pairs, both the radicals have been removed from the reaction.

25
Q

What would form if CH3Br was formed with another bromine radical attacking it?

A

Dihaloalkanes molecule would form

26
Q

What happens in further substitution?

A

This is when further substitution causes dihaloalkanes to form, with additional substituting removing hydrogens and substituting them for halogens e.g Br