27.2 Arenes: Physical properties, naming and reactivity Flashcards

1
Q

What state and colour is benzene at room temperature

A

. Colourless liquid at room temperature

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

Why does benzene have a much higher melting point than hexane

A

. It has flat hexagonal molecules which pack together very well in the solid state

They are therefore harder to separate and this must happen for the solid to melt

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

Are arenes soluble in water

A

. No because they are non-polar so don’t mix with water but do with other hydrocarbons and non polar solvents

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

How do you name aromatic compounds

With one substituent

A

Arenes are usually derivatives of benzene, so benzene forms root of the name

With one substituent eg CH3 in replace of H, C6H5CH3 is methylbenzene
Or with substituent Cl in replace of H it is chlorobenzene

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

How do you name aromatic compounds

With two substituents

A

Here, the ring is numbered.

So if two chlorines are added:
So 1,2-dichlorobenzene
Or 1,4-dichlorobenzene

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

Are aromatic compounds reactive

A

. The ring is an area of high electron density because of the delocalised bonding, and is therefore attacked by electrophiles

. The aromatic ring is very stable and needs energy to be put in to break the ring before the system can be destroyed.
This is called delocalisation energy, so the ring almost always remains intact in the reactions of arenes

So this means aromatic systems can undergo electrophilic substitution reactions

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