Organic chemistry - 4 Flashcards

1
Q

when oxidising an alcohol, what is the catalyst used?

A

acidified potassium dichromate (H+/Cr2O7^2-)

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

how can a carboxylic acid be made from an ester?

A

ester -(water)-> alcohol+ carboxylic acid

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

amide -(water)-> ?

A

amide -(water)-> carboxylic acid + salt

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

what three molecules can be broken down by hydrolysis to produce a carboxylic acid?

A
  • ester
  • amide
  • nitrile
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

three substances that form salts when reacted with carboxylic acids

A
  • some metals
  • carbohydrates
  • alkalis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

amine + carboxylic acid -(HEAT)-> ? + ?

A

amine + carboxylic acid -(HEAT)-> amide + water

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

what is an amine?

A

organic derivatives of ammonia where one or more hydrogen atoms in ammonia is replaced by alkyl group

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

what are the three classification of amines?

A

primary, secondary, tertiary

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

how are amines classified?

A

according to the number of alkyl groups attached to nitrogen

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

what do primary/secondary amines contain that allow them to have a higher b.p compared to their isomeric tertiary amines?

A

polar N-H bond - hydrogen bonds between molecules

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

why are amines known as weak bases?

A

lone pair of electrons on nitrogen atom accepts a proton from water molecule

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

what can amines react with to form salts?

A

mineral acids and carboxylic acids

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

what is the simplest aromatic hydrocarbon?

A

benzen (C6H6)

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

when benzene is added to bromine does the bromine decolourise?

A

no - benzene is more stable than typical unsaturated hydrocarbon

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

what type of hybridisation occurs in each carbon atom of benzene?

A

sp2 hybridisation

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

what do the three half-filled sp2 hybrid orbitals form in benzene?

A

σ bonds

17
Q

benzene: on each carbon atom there is an electron occupying a p orbital - what occurs due to this?

A

side-on overlap occurs and a π electron cloud is formed

18
Q

what bonds are there in a benzene molecule?

A
  • 12σ bonds

- π electron cloud that contains delocalised electrons

19
Q

why is benzene stable?

A

due to delocalised electrons

20
Q

what type of reaction do benzene molecules undergo?

A

electrophilic substitution reactions

21
Q

what are the 4 electrophilic substitution reactions that benzene can undergo?

A
  • alkylation
  • chlorination
  • nitration
  • sulfonation
22
Q

what is the reagent used in alkylation?

A

CH3Cl/AlCl3

23
Q

what is the reagent used in chlorination?

A

Cl2/FeCl2

24
Q

what is the reagent used in nitration?

A

c.HNO3 or c.H2SO4 acids

25
Q

what is the reagent used in sulfonation?

A

c. H2SO4

26
Q

what type of drug mimics the body naturally active molecule?

A

agonist

27
Q

how does an agonist work?

A

binds to receptor site and triggers same response as natural molecule

28
Q

what type of drug prevents the naturally active molecule from binding?

A

antagonist

29
Q

how does an antagonist work?

A
  • binds more strongly to receptor site

- blocks site and natural response not triggered