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1
MesomericMesomeric
Effect/Resonance EffectEffect/Resonance Effect
Amina Tariq
Pharm-D
15987
RIPS
2
INTRODUCTION OFINTRODUCTION OF
MESOMERISMMESOMERISM
THE CONCEPT OF MESOMERISM
MESOMER AND MESOMERIC
EFFECT WERE INTRODUCE BY
INGOLD IN 1938.
 IT IS ALSO KNOWN AS OLD
FASHIONED TERM FOR
RASONANCE
3
4
EXAMPLEEXAMPLE
Mesomeric Effect ( M-Effect)Mesomeric Effect ( M-Effect)
It refers to the polarity produced in a molecule
as a result of interaction between two pi bonds
or a pi bond and lone pair of electrons.
The electron withdrawing or releasing effect
attributed to a substituent through delocalization
of π electrons, which can be visualized by drawing
various canonical forms, is known as mesomeric
effect or resonance effect. It is symbolized by
M or R.
6
TYPESTYPES
Negative mesomeric effect (-M or -R):
 It is shown by substituents or groups that withdraw
electrons by delocalization mechanism from rest of
the molecule and are denoted by -M or -R. The
electron density on rest of the molecular entity is
decreased due to this effect.
E.g. -NO2, Carbonyl group (C=O), -C N,≡
-COOH, -SO3H etc.
 
 
7
Negative mesomeric effect (-M or -R):Negative mesomeric effect (-M or -R):
Example:
1) The negative resonance effect (-R or
-M) of carbonyl group is shown below. It
withdraws electrons by delocalization of π
electrons and reduces the electron density
particularly on 3rd carbon.
 
8
Negative mesomeric effectNegative mesomeric effect
(-M or -R):(-M or -R):
2) The negative mesomeric effect (-R or
-M) shown by cyanide group in
acrylonitrile is illustrated below. The
electron density on third carbon
decreases due to delocalization of π
electrons towards cyanide group.
9
10
Positive resonance orPositive resonance or
mesomeric effect (+M or +R):mesomeric effect (+M or +R):
  The groups show  positive mesomeric effect
when they release electrons to the rest of the
molecule by delocalization. These groups are
denoted by +M or +R. Due to this effect, the
electron density on rest of the molecular entity
is increased.
 E.g. -OH, -OR, -SH, -SR, -NH2, -NR2 etc
11
Positive resonance orPositive resonance or
mesomeric effect (+M or +R):mesomeric effect (+M or +R):
 The -NH2 group in aniline also exhibits
+R effect. It releases electrons towards
benzene ring through delocalization.
12
Positive mesomeric effect (+M or +R):Positive mesomeric effect (+M or +R):
1).In phenol, the -OH group shows +M effect
due to delocalization of lone pair on oxygen
atom towards the ring. Thus the electron
density on benzene ring is increased particularly
on ortho and para positions.
13
14
15
16
SIGNIFICANCESIGNIFICANCE
It describe the charge distribution in a
molecule ,thus provide an effective way of
determing the point of attack of
electrophiles and nucleophiles.
Useful in explaining physical
characteristics
i.e bond length,dipole moment.
17
18

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Mesomeric Effect

  • 1. 1
  • 3. INTRODUCTION OFINTRODUCTION OF MESOMERISMMESOMERISM THE CONCEPT OF MESOMERISM MESOMER AND MESOMERIC EFFECT WERE INTRODUCE BY INGOLD IN 1938.  IT IS ALSO KNOWN AS OLD FASHIONED TERM FOR RASONANCE 3
  • 4. 4
  • 6. Mesomeric Effect ( M-Effect)Mesomeric Effect ( M-Effect) It refers to the polarity produced in a molecule as a result of interaction between two pi bonds or a pi bond and lone pair of electrons. The electron withdrawing or releasing effect attributed to a substituent through delocalization of π electrons, which can be visualized by drawing various canonical forms, is known as mesomeric effect or resonance effect. It is symbolized by M or R. 6
  • 7. TYPESTYPES Negative mesomeric effect (-M or -R):  It is shown by substituents or groups that withdraw electrons by delocalization mechanism from rest of the molecule and are denoted by -M or -R. The electron density on rest of the molecular entity is decreased due to this effect. E.g. -NO2, Carbonyl group (C=O), -C N,≡ -COOH, -SO3H etc.     7
  • 8. Negative mesomeric effect (-M or -R):Negative mesomeric effect (-M or -R): Example: 1) The negative resonance effect (-R or -M) of carbonyl group is shown below. It withdraws electrons by delocalization of π electrons and reduces the electron density particularly on 3rd carbon.   8
  • 9. Negative mesomeric effectNegative mesomeric effect (-M or -R):(-M or -R): 2) The negative mesomeric effect (-R or -M) shown by cyanide group in acrylonitrile is illustrated below. The electron density on third carbon decreases due to delocalization of π electrons towards cyanide group. 9
  • 10. 10
  • 11. Positive resonance orPositive resonance or mesomeric effect (+M or +R):mesomeric effect (+M or +R):   The groups show  positive mesomeric effect when they release electrons to the rest of the molecule by delocalization. These groups are denoted by +M or +R. Due to this effect, the electron density on rest of the molecular entity is increased.  E.g. -OH, -OR, -SH, -SR, -NH2, -NR2 etc 11
  • 12. Positive resonance orPositive resonance or mesomeric effect (+M or +R):mesomeric effect (+M or +R):  The -NH2 group in aniline also exhibits +R effect. It releases electrons towards benzene ring through delocalization. 12
  • 13. Positive mesomeric effect (+M or +R):Positive mesomeric effect (+M or +R): 1).In phenol, the -OH group shows +M effect due to delocalization of lone pair on oxygen atom towards the ring. Thus the electron density on benzene ring is increased particularly on ortho and para positions. 13
  • 14. 14
  • 15. 15
  • 16. 16
  • 17. SIGNIFICANCESIGNIFICANCE It describe the charge distribution in a molecule ,thus provide an effective way of determing the point of attack of electrophiles and nucleophiles. Useful in explaining physical characteristics i.e bond length,dipole moment. 17
  • 18. 18