Reactions of alcohols Flashcards

1
Q

what are alcohols?

A

molecules with -OH bonded to a C chain

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

what can alcohols with small C chains do?

A

they are soluble in water, since they can form H bonds with H2O

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

what happens to primary alcohols when heated with acidified potassium dichromate, K2Cr2O7/H+?

A
  • they are oxidised in 2 stages
  • first to an aldehyde, then to a carboxylic acid
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

if you heat a primary alcohol with acidified potassium dichromate, K2Cr2O7/H+, but you only want the aldehyde, what do you need to do?

A

you need to limit the oxidation
- use the minimum amount of oxidising agent
- distill the product straight out of the mixture as it forms

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

what is the balanced equation for the reaction of primary alcohols with acidified potassium dichromate, K2Cr2O7/H+?

A

Ch3CH2OH + [O] => CH3CHO + H2O

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

so we get a carboxylic acid from a primary alcohol and acidified potassium dichromate, what do we need to ensure the oxidation goes as far as possible?

A
  • use excess oxidising agent
  • heat the mixture under reflux
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is reflux?

A

boiling liquid re-agents with a vertical condenser attached, prevents loss of reactants and products

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

what is the balanced equation from getting carboxylic acid from heating a primary alcohol with acidified potassium dichromate?

A

CH3CH2OH + 2[O] -> CH3COOH + H2O

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

what happens when you heat a secondary alcohol with acidified potassium dichromate?

A

oxidised in one step making a ketone

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

what happens when you heat a tertiary alcohol with acidified potassium dichromate?

A
  • cannot be oxidised as there is no C-C bond to be broken
  • no colour change from orange to green
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what do you see if acidified potassium dichromate gets oxidised?

A

a colour change from orange to green as the acidified potassium dichromate gets reduced to Cr 3+

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

what are the conditions and reagents required for the dehydration of alcohols?

A
  • pass vapour of the alcohol over a heated aluminium catalyst (Al2O3)
    or
  • heat under reflux with concentrated H2SO4
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what is an elimination reaction (eg. dehydration of alcohol)?

A

an elimination reaction is one in which a small molecule is removed from a larger molecule giving an unsaturated molecule (alkene)

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

what is esterification?

A

esters can be made from an alcohol and a carboxylic acid, the reaction is reversible
alcohol + carboxylic acid <=> ester + h2o

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

what are the conditions needed for esterification?

A

heat under reflux with an acid catalyst (either c. HCl or c. H2SO4)

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