18A.4 Flashcards

1
Q

What is phenol

A

a hydroxyl group attached to a benzene ring with similar properties to an aliphatic alcohol like ethanol.

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

why do we expect that phenol would undergo electrophilic substitution

A

since it contains a benzene ring

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

most aromatic compounds have

A

a benzene ring and a aliphatic part

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

what is the difference between Bromination of benzene and Bromination of phenol

A
  1. Bromination of benzene is slow and requires a catalyst and heating under reflux, while the Bromination of phenol works at room temp, with no catalyst
  2. Bromination of phenol works with bromine water as it decolorizes it but benzene cant do that
  3. the substitution in the Bromination of phenol is by 3 Br while benzene is just 1
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

for the Bromination of phenol by bromine water what is observed

A

the decolorizing of the bromine water, and the formation of a white precipitate caused by the organic compound

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

what is the reaction for the Bromination of phenol by bromine water

A

page 230

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

what is the name of the white organic precipitate formed in the reaction of the Bromination of phenol by bromine water

A

2,4,6-tribromophenol

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

how are the carbons number when naming a aromatic compound

A

clockwise with Oh being on the first carbon

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

why is Bromination of phenol more readily than Bromination of Benzene

A

that is because
* the lone pair of electrons on the Pz-orbital on the oxygen in the OH group interacts with the delocalized pi-bond electrons in the ring.
* then the electron density above and below the ring of atoms increase, in a process called ‘activation’ since the molecule is now much more reactive towards electrophiles
*Bromine molecules, which are originally non-polar, are polarized as the approach the benzene ring. eventually the Br—Br bond is broken forming Br+ electrophile that attacks the benzene ring

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

why is the process where the electron density of phenol is increased called activation

A

since the molecule is now much more reactive towards electrophiles

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

what are the uses of phenol

A
  • antiseptics surgery: as with time many other antiseptics were developed from phenol such as the product of the chlorination of phenol (2,4,6 trichlorophenol) known as antiseptic TCP

-manufacture of polymers

-manufacture of pharmaceuticals

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

when benz is used in naming a organic compound it usually comes

A

after the other groups of the molecule

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