Halogenoalkanes Flashcards

(40 cards)

1
Q

How do you name a halogenoalkane with more than one halogen?

A

Alphabetically

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

What is the prefix for a halogenoalkane?

A

Iodo-
Bromo-
Chloro-

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

What are the three groups that halogenoalkanes can be classed into?

A

Tertiary
Primary
Secondary

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

What is a primary halogenoalkane?

A

One carbon is attached to the carbon atom that is joined to the halogen.

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

What is a secondary halogenoalkane?

A

Two carbons are attached to the carbon atom that is joined to the halogen.

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

What is a tertiary halogenoalkane?

A

Three carbons are attached to the carbon atom that is joined to the halogen.

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

What kind of reactions can halogenoalkanes undergo?

A

Elimination or Nucleophillic substitution

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

What is substitution?

A

Swapping a halogen atom for another atom or group of atoms.

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

What is a nucleophile?

A

An electron pair donator.

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

Give 3 nucleophile examples.

A

:OH-
:NH3
:CN-

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

What do the curly arrows show?

A

The movement of the pair of electrons.

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

Where does the curly arrow start and end?

A

From the lone pair of electrons to the carbon atom. Then from the bond between the carbon and the atom that is being substituted to the atom that is being substituted.

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

What does the rate of a substitution reaction depend on?

A

The strength of the C-X bond. The weaker the bond, the easier it is to break and the faster the reaction.

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

In group 7, which element forms the weakest C-X bond and which forms the strongest?

A

Iodine is the weakest and fluorine is the strongest.

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

Define hydrolysis?

A

The splitting of a water molecule by a reaction with water.

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

What is formed from a nucleophilic substitution with aqueous hydroxide ions?

A

Alcohol

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is the condition needed when using aqueous hydroxide ions?

A

In warm aqueous solution.

18
Q

What does a reaction with CN form?

19
Q

What is the reagent needed for the nucleophillic reaction with cyanide ions?

A

KCN dissolved in ethanol

20
Q

What is the condition needed when using cyanide ions?

A

Heating under reflux

21
Q

Where does the nitrile functional group have to be?

A

At the end of the group.

22
Q

How would you name a nitrile with 4 carbons?

A

ButanEnitrile.

23
Q

What is formed from a nucleophilic substitution with ammonia?

24
Q

What is the reagent needed for the nucleophilic substitution with ammonia?

A

NH3 dissolved in ethanol.

25
What is the condition needed for the nucleophilic substitution with ammonia?
Heating under pressure.
26
How could you minimise a lower yield of ammonia?
Use excess ammonia
27
What is elimination?
Removal of a small molecule from the organic molecule.
28
What reagent is needed for the elimination reaction with alcoholic hydroxide ions?
Potassium or sodium hydroxide
29
What condition is needed for the elimination reaction with alcoholic hydroxide ions?
In ethanol and heated.
30
What can be formed from unsymmetrical secondary and tertiary halogenoalkanes?
Two or three different structural isomers.
31
What are chloroalkanes and chlorofluoroalkanes used as?
Solvents
32
What are halogenoalkanes used as?
Refrigerants Pesticides Aerosol propellants
33
Why have the uses of halogenoalkanes stopped?
They're toxic and have detrimental effects on the atmosphere.
34
Why is the ozone in the upper atmosphere beneficial?
It absorbs UV radiation.
35
What does ozone do in the lower atmosphere?
It is a pollutant and contributes towards the formation of smog.
36
What did man-made chlorofluorocarbons cause?
A hole in the ozone layer to form.
37
How are chlorine radicals formed in the upper atmosphere?
When energy from UV radiation causes C-Cl bonds in chlorofluorocarbons to break.
38
Suggest two reasons why the use of CFCs was not restricted until several years after Rowland and Molina published their research.
Lack of evidence that ozone was being depleted. Lack of alternatives to CFCs.
39
State how greenhouse gases contribute to global warming (CFCs).
Absorbs infrared radiation because it is a polar molecule.
40
What is the role of hydroxide ions?
Base