CHAPTER 12 - ALKANES Flashcards

1
Q

What is the general formula for alkanes

A

CnH2n+2

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

Are alkanes saturated or unsaturated hydrocarbons

A

Saturated

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

What bond is present in alkanes

A

Single covalent bonds, Sigma bonds

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

What is a covalent bond

A

A shared pair of electrons

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

What is a Sigma bond

A

The overlapping of two orbitals, one from each bonding atom

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

How many sigma bonds does each carbon have

A

4

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

What is the shape arrangement around each atom and their bonding angle

A

Tetrahedral, 109.5

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

How is crude oil separated

A

Fractional distillation (in a distillation tower)

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

Why does the boiling point increase as carbon chain length increases?

A

Increase in Intermolecular forces (LDFs)
As chain length increases, molecules have larger surface area, and greater contact is possible, hence more energy is required to overcome forces

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

What effect does branching have on boiling point and why

A

Boiling point decreases as branching increases

Fewer points of contact between molecules of branched molecules, giving fewer London forces

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

Kerosene is obtained from crude oil. Name the process used to obtain kerosene from crude oil and explain how the process works

A

Factional distillation

Different fractions have different boiling points

Increase the temperature of the system so each fraction vaporises separately and other fractions can be collected

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

Explain why the straight-chain isomer of C10H22 has higher boiling point than any of its branched-chain isomers

A

There is more surface contact between straight-chain isomer so it has more/stronger London forces

More energy required to break these London forces

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

Explain why the boiling points increase down the alkane homologous series

A

As the chain length increases, there are more points of contact between molecules, meaning more London forces

More energy is required to break these bonds

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

Describe the bonding in ethane. State and explain the H-C-H bond angle in a molecule of ethane

A

Single bonds between the C-C and the C-H are sigma bonds

Sigma bonds is the overlap of orbitals, one from each bonding atom

Each carbon atom is bonded to four other atoms by covalent bonds.

The shape around each carbon atom is tetrahedral.

The four bonding pairs of electrons repel equally to give a bond angle of 109.5 around the carbon atom

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

Why are alkanes relatively unreactive

A

C-C and C-H bonds are strong

C-C bonds are non-polar

C-H bonds are non-polar as their electronegativity is very similar

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

What does the complete combustion of alkanes form

A

Carbon dioxide and water

17
Q

Methane 193

A
18
Q

What is the equation for balancing complete combustion of any alkene

A

CxHy + (x+y/4)O2 —> xCO2 + y/2 H2O

19
Q

What are the products from Incomplete combustion of alkanes

A

Carbon monoxide (or carbon) and water

20
Q

Write the equation for the incomplete combustion of methane

A

CH4 + 1.5O2 —> CO + 2H2O
OR
CH4 + O2 —> C + 2H2O

21
Q

How do Alkanes react with halogens in present of High energy UV radiation

A

Substitution reaction

eg. CH4 + Br2 —. CH3Br + HBr

22
Q

What is the type of reaction mechanism for the (photo)bromination of Alkanes

A

(Free) Radical substitution

23
Q

What are the 3 Stages for Free radical substitution of Bromine to an Alkane

A

Initiation, Propagation, Termination

24
Q

What is the Equations in each stage of Photobromination of alkanes (eg. Methane)

A

Initiation:
Br2 —> 2Br * (dot)
Propogation:
CH4 + Br* —> CH3* + HBr
CH3* + Br2 —> CH3Br + Br*
Termination:
Br* + Br* —> Br2
CH3* + CH3* —> C2H6
CH3* + *Br —> CH3Br
(pg 196)

25
Q

How does further substitution occur in photobromination

A

More Bromine radicals an collide with bromomethane (eg.) substituting more hydrogens

leaving a mixture of CH4, CH3Br, CH2Br2, CHBr3 and CBr4

26
Q

Explain why the alkanes do not react with common laboratory reagents

A

Alkanes are fairly unreactive due to the presence of strong C-H and C-C bonds which have little or no polarity