,
, bon
onding formed by overlap of
patomic orbitals (f from
each of the 6
c atoms)
·
maximum overlap :
benzene
molecules planar
lobes of the p orbitals overlap
ring of delocalised es above
+
=>
below plane of catoms
I
ring of delocalised es
↓
delocalised es in benzene cannot conduct
electricity
Naming any I compounds
I
Functional groups substituted in place of H-atom
6 2
directly
CI
5 3
I NOz OH
I
O pheno on 1
Br-- Br
:
don't have
4
to state
Chlorobenzene Nitrobenzene phenol
I
Br
↓
2, 4 6-tribromopheno
NHz
,
↑
COOH
-
Cl
Phenylamine 1, 3-dimethylbenzene 2-chlorobenzoic acid
Phenyl group :
CH5 X
functional group
,
, bon
onding formed by overlap of
patomic orbitals (f from
each of the 6
c atoms)
·
maximum overlap :
benzene
molecules planar
lobes of the p orbitals overlap
ring of delocalised es above
+
=>
below plane of catoms
I
ring of delocalised es
↓
delocalised es in benzene cannot conduct
electricity
Naming any I compounds
I
Functional groups substituted in place of H-atom
6 2
directly
CI
5 3
I NOz OH
I
O pheno on 1
Br-- Br
:
don't have
4
to state
Chlorobenzene Nitrobenzene phenol
I
Br
↓
2, 4 6-tribromopheno
NHz
,
↑
COOH
-
Cl
Phenylamine 1, 3-dimethylbenzene 2-chlorobenzoic acid
Phenyl group :
CH5 X
functional group
,
