ORGANIC CHEMISTRY - ALCOHOLS Flashcards

1
Q

what is the functional group of an alcohol?

A

-OH hydroxyl group

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

what is a general formula for an alcohol

A

CnH2n+1OH

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

how do you name alcohols (prefix and suffix)?

A

hydroxyl. - prefix
ol - suffix

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

what kind of intermolecular forces do alcohols have? why?

A

they have hydrogen bonding due to the high difference in electronegativity between O and H and vander waals forces

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

how do alcohols MP and BP compare to other hydrocarbons with the same chain length?

A

alcohols have higher MP and BP because the hydrogen bonding requires more energy to break the bonds.

Hydrogen bonding is stronger than the London forces.

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

are alcohols soluble in water? is solubility affected by chain length?

A

shorter chain alcohols are soluble in water because the OH forms hydrogen bonds with the water molecules.

Insoluble when it is a long chain due to the non polarity of the long hydrocarbon chain which takes precedence.

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

what makes an alcohol primary?

A

when the carbon attached to the OH is attached to one other carbon atom.

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

what makes an alcohol secondary?

A

when the carbon attached to the OH is attached to two other carbon atoms.

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

what makes an alcohol tertiary?

A

when the carbon attached to the OH is attached to 3 other carbon atoms.

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

how can ethanol be made from crude oil?

A

hydration of ethene via electrophilic addition (phosphoric acid catalyst.)

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

what are the advantages of this method?

A

+ fast
+ continuous

  • not renewable as made from crude oil
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

how can ethanol be made from fermentation?

A

plant carbohydrates are broken down and fermented by enyzmes in yeast = alcohols

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

what conditions are needed for fermentation to take place?

A

enzymes in yeast as catalyst
35 degrees
anaerobic conditions

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

write an equation for fermentation reaction?

A

C6H12O6 –> 2C2H5OH + 2CO2

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

advantages and disadvantages of fermentation method?

A

+ renewable as from plants
- slow batches
-slow process
- alcohol solution not pure and needs to be fractionally distilled

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

how can an alkene be made from alcohol?

A

dehydration - elimination reaction of alcohol

not economical at the moment

17
Q

what is an elimination reaction?

A

the removal of a smaller molecule from a larger one

18
Q

which group leaves the parent molecule in dehydration of alcohols?

A

OH and H to form a water

19
Q

what physical conditions are needed for the elimination reaction from alcohols to alkenes?

A

excess hot concentrated sulphuric acid

20
Q

draw a mechanism for the dehydration of alcohol

A

diagram on pmt

21
Q

what forms if you partially oxidise a primary alcohol?

A

an aldehyde

22
Q

what conditions are needed to partially oxidise a primary alcohol?

A
  • dilute sulphuric acid
  • potassium dichromate = oxidising agent
  • distill product as it is produced
  • gentle heating
23
Q

write an equation for the partial oxidation of ethanol?

A

CH3CH2OH(l) + [O] —> CH3CHO(g) + H2O(l)

24
Q

what forms if you fully oxidise an alcohol?

A

a carboxylic acid

25
Q

what conditions are needed to fully oxidise a primary alcohol?

A
  • concentrated sulphuric acid
  • potassium dichromate = oxidising agent
  • heating under reflux
26
Q

write an equation for the full oxidation of ethanol?

A

CH3CH2OH(l)+ 2[O] —> CH3COOH(g) + H2O(l)

27
Q

what forms if you oxidise a secondary alcohol?

A

a ketone

28
Q

why cant a secondary alcohol be oxidised further and why cant a tertiary alcohol be oxidised?

A

a carbon-carbon bond would have to break

29
Q

what conditions are needed for the oxidation of a secondary alcohol?

A
  • concentrated sulphuric acid
  • potassium dichromate
  • heat under reflux
30
Q

write an equation for the oxidation of propan-2-ol?

A

CH3CH(OH)CH3 (l) +[O] —> CH3COCH3 (g) + H2O

31
Q

what is an aldehyde? what is its functional group?

A

molecule with C=O group at the end of the carbon chain, carbonyl functional group (C=O)

32
Q

what is a ketone? what is its functional group?

A

molecule with C=O group in the middle of the carbon chain, carbonyl functional group (C=O)

33
Q

What does the Tollens’ test give a positive result for?

A

Aldehydes

34
Q

What is in Tollens’ reagent? How does this react with the substance to be tested?

A

Tollens’ reagent - silver nitrate
Aldehyde - oxidised to COOH, forms a silver mirror
Ketone - no silver mirror

35
Q

How do you carry out the Tollens’ test?

A

Add equal volume of substance being tested and Tollens’ reagent to a test tube. Leave in water bath for 10 mins and observe any changes.