WM 1- Devlopment Of Modern Medicines Flashcards

1
Q

Why are alcohols polar molecules?

A

Because of O-H bond

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

Why does solubility of alcohols decrease as chain length increases?

A

Less efficient hydrogen bonding

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

Define primary alcohol

A

Alcohol in which OH is bonded to a carbon which is bonded to 0 or 1 other carbon

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

Define tertiary alcohol

A

Alcohol in which OH is bonded to carbon which is bonded to 3 others carbons

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

What oxidising agent is used to oxidise alcohols?

A

Acidified potassium dichromate

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

What happens to the dichromate ion when alcohols are oxidised?

A

Turn from orange to green chromate ions

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

What is the difference between ‘distillation’ and ‘heating under reflux’?

A
  • in distillation, mixture is heated and products evaporate down horizontal condenser tube into flask
  • in heating under reflux, products evaporate in vertical condenser tube, so condense and return to mixture
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is produced when primary alcohols are oxidised by distillation, and what is its structure?

A
  • aldehydes
  • carbonyl (C=O) is at end of chain
  • general formula RCHO
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is produced when primary alcohols are heated under reflux and what is its structure?

A
  • carboxylic acid
  • carbon at end is attached to O and OH
  • general formula RCOHO
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What is produced when secondary alcohols are oxidised and what is their structure?

A
  • ketones
  • carbonyl group (C=O) is in middle of chain
  • general formula RCOR
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What is produced when tertiary alcohols are oxidised and what is their structure?

A
  • do not oxidise, as C does not have a hydrogen atom to which OH is attached
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Propan-1-al is an example of what?

A

Aldehyde

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

What does dehydration of alcohol involve?

A

Elimination of water from alcohol to form an alkene

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

What are the conditions required for dehydration of an alcohol?

A
  • 300 degrees

- heated catalyst of Alumnia, Al2O3 OR conc sulfuric acid

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

What do substitution reactions with alcohols involve? And what are the conditions needed?

A

Nucleophilic substitution with halide ions

- presence of strong acid

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

What are esterification reactions between?

A

Carboxylic acid OR acid anhydride + alcohol = ester and water

17
Q

What is the general formula for esters?

A

R-COOC-R

18
Q

What is an ether and what is the general formula?

A

Functional group isomers of alcohols

- gen formula C-O-C

19
Q

Why are acid anhydrides better to use in esterification than carboxylic acids?

A
  • give higher yields

- more reactive