Alcohols Flashcards

1
Q

What is a primary alcohol?

A

An alcohol in which the OH group is attached to a carbon which is attached to just one other carbon atom.

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

What is a secondary alcohol?

A

An alcohol in which the OH group is attached to a carbon which is attached to two other carbon atoms.

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

What is a tertiary alcohol?

A

An alcohol in which the OH group is attached to a carbon which is attached to three other carbon atoms.

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

Describe the trend of boiling points in homologous series.

A

Boiling point increases as molecules get larger as bigger molecules form stronger London forces which take more energy to break.

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

Why do alcohols have anomalously high boiling points?

A

They contain hydrogen bonds between the lone pair on oxygen atoms and the delta + charges on hydrogen atoms.

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

Why are alcohols soluble in water.

A

They can form hydrogen bonds with water molecules.

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

Explain the trend of solubility in the alcohols.

A

As molecules get larger, solubility decreases, as only one hydrogen bond can form per alcohol molecule.

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

What are the products of complete combustion of alcohols?

A

Carbon dioxide and water.

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

Why is ethanol a good fuel?

A

It contains oxygen, so burns cleanly with little incomplete combustion.
It can be produced naturally via fermentation so is renewable.
It is a liquid so easy to store.

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

Give the conditions for the dehydration of alcohols

A

Heat under reflux

Concentrated sulphuric/ phosphoric acid catalyst

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

What does elimination mean?

A

The removal of atoms or groups from neighbouring carbon atoms to form an alkene and release a small molecule (eg water)

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

Which is the easiest type of alcohol to eliminate water from?

A

Tertiary

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

Describe the dehydration of alcohols.

A

An alcohol is heated with a concentrated acid catalyst to give a C=C double bond and a water molecule

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

What are the two chemicals required to oxidise and organic compound?

A
Potassium dichromate (K2Cr2O7)
Dilute sulphuric acid
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What can be observed when an organic molecule is oxidised?

A

Solution changes from orange to green (or blue).

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

What are the potential products of oxidation of primary alcohols?

A

Aldehydes or carboxylic acids.

17
Q

How is the oxidising agent shown in an oxidation reaction?

18
Q

Give a general equation for the formation of an aldehyde from a primary alcohol.

A

primary alcohol + [O] —–> aldehyde + water

19
Q

What are the conditions for oxidising a primary alcohol to an aldehyde?

A

Heat and distillation.

20
Q

Give a general equation for the formation of a carboxylic acid from a primary alcohol.

A

primary alcohol + 2[O] ——-> carboxylic acid + water

21
Q

Give a general equation for the formation of a carboxylic acid from an aldehyde.

A

aldehyde + [O] ——-> carboxylic acid

22
Q

What is the product of the oxidation of a secondary alcohol?

23
Q

Give a general equation for the formation of a ketone from a secondary alcohol.

A

secondary alcohol + [O] ——> ketone + water

24
Q

What are the conditions for oxidising a primary alcohol to a carboxylic acid?

A

Heat under reflux

25
What are the conditions for oxidising a secondary alcohol to a ketone?
Heat under reflux
26
Why can a tertiary alcohol not be oxidised?
The C atom that holds the -OH group already has 4 bonds- there are no hydrogen atoms to be displaced.
27
What is the mechanism by which hydrogen halides react with alcohols?
Nucleophilic substitution
28
What species acts as the nucleophile in the substitution of halogens onto alcohols?
The delta- halogen atom.
29
What is the advantage of using alcohols to produce haloalkanes?
The halogen atom can be directed onto a specific carbon atom, with no risk of the production of stereoisomers.
30
What are the conditions for the nucleophilic substitution of alcohols?
Heat under reflux
31
What are the reagents in the process of esterification?
An alcohol and a carboxylic acid
32
What are the conditions for the process of esterification?
Heat under reflux and a concentrated sulphuric acid catalyst.
33
Give a general reaction for the production of esters
Alcohol + carboxylic acid ester + water
34
How are esters named?
(alcohol) yl (acid) oate
35
What is the functional group of an ester?
-COO- | A carbon atom attached to both an OH group and a single oxygen atom which forms part of the carbon chain.
36
In the nucleophilic substitution of alcohols, how is the HX nucleophile formed?
NaX + H2SO4 ------> HBr + NaHSO4
37
Give the reagents for the nucleophilic substitution of an alcohol with a halogen.
Sodium halide, sulphuric acid and an alcohol.