M4 Chapter 12 - Alkanes Flashcards

1
Q

What is an alkane?

A

A saturated hydrocarbon containing C-H bonds only joined together by single covalent bonds.

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

What is the general formula of alkanes?

A

CnH2n+2

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

Are alkane bonds polar?

A

No because Carbon and Hydrogen have similar electronegativities.

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

What type of covalent bonds are present?

A

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

The sigma bond is a covalent bond which has a direct overlap of the electron clouds of the bonding atoms.

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

What is the shape and angle of an alkane?

A

Tetrahedral (4 bonding regions)
109.5

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

What do the sigma bonds allow for in alkanes?

A

They can act as axes around which the atoms can rotate freely. Meaning the shapes are not rigid.

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

What type of intermolecular force do alkanes have? Why?

A

London forces because they are non polar.

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

How to separate crude oil (hundreds of different alkanes) apart?

A

Fractional Distillation.

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

What happens to the boiling points as alkane chain length increases? Why?

A

The boiling point increases as there is more surface area meaning more surface contact between molecules. This make more induced dipole-dipole interactions. Therefore, more energy is required to overcome the forces.

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

Does a branched molecule have a lower or higher boiling point compared to equivalent straight chain. Why?

A

The branched molecule has a lower boiling point because they have lower surface contact between molecules meaning fewer London Forces. Therefore, lower amount of heat to break these weaker bonds.

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

Are alkanes soluble in water? Why?

A

Insoluble because the hydrogen bonds in water are stronger than alkanes’ London forces of attraction.

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

How reactive are alkanes? Why?

A

Very unreactive due to C-C and C-H bonds being strong and the electronegativity of both C and H being so similar that they are considered non-polar.

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

What reaction will alkanes undergo?

A

Combustion and reactions with halogens.

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

What type of reaction is combustion?

A

Oxidation

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

What is complete combustion?

A

Combustion that occurs with a plentiful supply of oxygen to form Carbon Dioxide and Water.

17
Q

What are the products of complete combustion?

A

Carbon Dioxide and Water

18
Q

What is the colour of the bunsen burner during complete combustion?

A

Blue Flame

19
Q

What is incomplete combustion and what products are formed in the case of alkanes?

A

Combustion in a limited supply of oxygen.
Products are Carbon Dioxide, Water, Carbon Monoxide.

20
Q

Write an equation for the complete combustion of propane.

A

C3H8 + 5O2 –> 3CO2 + 4H2O

21
Q

What type of hydrocarbon are most likely to undergo incomplete combustion?

A

Longer chained hydrocarbons as more moles (amounts) of oxygen are required for the same reaction.

22
Q

What is the environmental impact of Carbon Monoxide?

A

Toxic/Poisonous

23
Q

What is the environmental impact of soot?

A

Asthma, Cancer, Global Dimming

24
Q

How are halogenoalkanes formed from alkanes? (Mechanism)

A

Free Radical Substitution

25
In the presence of what does alkanes react with halogens?
UV Light
26
State and explain what the 3 stages of free radical substitution are.
Initiation = Breaking the halogen bond to form free radicals Propagation = Chain reaction part where products are formed but the radical remains Termination = Free radicals are removed, stable products are formed.
27
Write equations for the reaction of CH4 with Cl2 to form Ch3Cl
Cl2 --> Cl· + Cl· --------------------------------- Cl· + CH4 --> HCl + ·CH3 ·CH3 + Cl2 --> CH3Cl + Cl· --------------------------------- ·CH3 + Cl· --> CH3Cl 2Cl· --> Cl2 ·CH3 + ·CH3 --> CH3CH3
28
What type of reaction is free radical substitution?
Substitution Reaction
29
Explain Initiation.
The covalent bond in the halogen is broken via homolytic fission. Where the energy for this bond fission is provided by UV Light.
30
What is a radical?
A very reactive species with an unpaired electron.
31
Explain Propagation.
The reaction undergoes a series of 'chain' reactions. Specifically, in the first part a methyl radical is formed. In the second part, each methyl radical reacts with another halogen molecule to form the organic product with another halogen radical.
32
Explain Termination.
Two radicals collide, forming a molecule with all electrons paired. Eg: ·Br + ·Br --> Br2
33
What are the limitations of radical substitution in organic synthesis?
· Further substitution where in theory all hydrogens can be replaced with halogens. · Substitution at different points in the Carbon chain.