Chemistry > Aromatic Compounds > 9.0 Ortho / Para Ratio
Aromatic Compounds
1.0 The Structure of Benzene
1.1 A Resonance Picture of Benzene
1.2 The Stability of Benzene
1.3 The Resonance Explanation of the Structure of Benzene
1.4 Bond lengths and angles in benzene
1.5 Hückle’s Rule: The $\left( {4n{\text{ }} + {\text{ }}2} \right)\pi $ Electron Rule
2.0 Electrophilic Aromatic Substitution Reactions
3.0 Nitration
4.0 Sulphonation
5.0 Halogenation
6.0 Friedel-Crafts Alkylation
7.0 Friedel-Crafts Acylation
8.0 Orientation and Reactivity in Electrophilic Aromatic Substitution
8.1 Donation of electrons into a benzene ring by resonance
8.2 Withdrawal of electrons from a benzene ring by resonance
9.0 Ortho / Para Ratio
9.1 Directive influence of the groups during substitutions in benzene ring
9.2 Mechanism of o and p-directing groups
9.3 Mechanism of o- and p-directing groups not have unshared pair of electrons
9.4 Mechanism of o- and p-directing gps having unshared pair of electron(s)
9.5 Mechanism of m-directing groups
9.6 Competitive orienting effect of two substituents
10.0 Reactions of Alkyl Benzenes
9.1 Directive influence of the groups during substitutions in benzene ring
1.2 The Stability of Benzene
1.3 The Resonance Explanation of the Structure of Benzene
1.4 Bond lengths and angles in benzene
1.5 Hückle’s Rule: The $\left( {4n{\text{ }} + {\text{ }}2} \right)\pi $ Electron Rule
8.2 Withdrawal of electrons from a benzene ring by resonance
9.2 Mechanism of o and p-directing groups
9.3 Mechanism of o- and p-directing groups not have unshared pair of electrons
9.4 Mechanism of o- and p-directing gps having unshared pair of electron(s)
9.5 Mechanism of m-directing groups
9.6 Competitive orienting effect of two substituents
(a) The position of new incoming group (guest) in ${C_6}{H_6}$ nucleus is decided by the group already present in nucleus (host). This is known as directive influence of the host group present in the nucleus.
(b) Directive influence of the host group is of two types i.e. the group already present in nucleus during further substitution of a group acts as
(i) either ortho and para directing nature
(ii) or meta directing nature
(c) On the basis of their directive influence, the substituents have been classified as:
‘o’- and ‘p’- directing groups: $-N{H_2},{\text{ }}-NHR,{\text{ }}-N{R_2},{\text{ }}-OH,{\text{ }}-OR,{\text{ }}-SH,{\text{ }}-SR,{\text{ }}-C{H_3},-C{H_2}R,{\text{ }}-CH{R_2},{\text{ }}-C{R_2},{\text{ }}-{C_6}{H_5},{\text{ }}-Cl,{\text{ }}-Br,{\text{ }}-I,{\text{ }}-C{H_2}OH,{\text{ }}-C{H_2}Cl,{\text{ }}-C{H_2}N{H_2},{\text{ }}-C{H_2}CN,{\text{ }}-C{H_2}COOH,{\text{ }}-CH{\text{ }} = {\text{ }}CH{\text{ }}-{\text{ }}COOH$
‘m’-directing groups: $-N{O_2},{\text{ }}-S{O_2}H,{\text{ }}-S{O_2}Cl,{\text{ }}-CHO,{\text{ }}-COOH,{\text{ }}-COOH,{\text{ }}-COCl,-COOR,{\text{ }}-COR,{\text{ }}-COCOOH,{\text{ }}-CC{l_3},{\text{ }}-{N^ + }{H_3},{\text{ }}-{N^ + }{H_2}R,{\text{ }}-{N^ + }{R_3}$