1
B.Sc. First year
Students
Semester – I
Unit-IV
(D) Orientation
by
Dr Pramod R Padole
2
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
Unit IV- Aromatic Hydrocarbons
Orientation: Effect of substituent groups. Activating and
deactivating groups.
Theory of reactivity and orientation on the basis of inductive
and resonance effects (-CH3, -OH, -NO2 and –Cl groups).
D
Nomenclature and Isomerism of Aromatic Compounds:
Structure of Benzene: Kekule structure and Molecular orbital structure.
A
Aromaticity and Huckel’s rule Aromatic, antiaromatic and
non-aromatic systems
B
Mechanism of Electrophilic Aromatic Substitution: Nitration,
Friedal Craft Alkylation and Acylation.Nuclear and Side Chain
Halogination, Birch Reduction
C
LOGO
D) Orientation:
The process of determine the position of substituent in the
substituted benzene is called orientation.
Or The relative arrangement of atoms or groups on the
aromatic ring is called orientation.
By Dr Pramod R Padole
Orientation:
Defination: The process of determine the position of substituent in
the substituted benzene is called orientation.
Or
Defination: The relative arrangement of atoms or groups on the
aromatic ring is called orientation.
 The new group is located either ortho, meta or para positions to the
existing substituent (first/original).
 The identity of the first substituent determines the position of the
second substituent.
 Substitution in Mono-substituted Benzene:
By Dr Pramod R Padole
Effect of Substituent groups on further
Electrophilic Substitution:
Directing
(or orienting)
influence
Effect
Of
Substituent
Activity effect
(or influence)
There are two types of influence of substituent's:
Directing (or orienting) influence:
Substituent group, X, directs the incoming
group, Y, either to ortho and para positions
or only to m-position.
 This effect of group already present (-X)
on the benzene ring is known as orienting
(directive) influence of the group or
orientation effect.
pramodpadole@gmail.com
By Dr Pramod R Padole
Directing (or orienting) influence:
Ortho-Para
(o/p) Directing
Groups:
or
o-p directors:
Directing
(Orienting)
influence
meta
(m)
Directing Groups:
or
m directors:
The substituent groups are thus classified into two types.
Ortho-para directing groups or o-p directors:
Ortho-para directing groups or o-p directors:
The group (first substituent) which directs the second
incoming group (i.e. second substituent) to the ortho-para
(o-p) positions of the aromatic ring or benzene ring
simultaneously are called ortho-para directing groups or
o-p directors.
Q.1) Explain: Ortho-Para directing groups with a suitable example. (S-04, W-05 & S-06, 2 Mark)
Q.2) Define with a suitable example: Ortho-Para directing groups. (S-12 & W-13, 2 Mark)
Ortho-para directing groups or o-p directors:
Ortho-para directing groups or o-p directors:
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
Ortho-para directing groups or o-p directors:
CH3
Toluene
+ I effect
Ortho-para directing groups or o-p directors:
Directive influence of o, p-directing groups:
 Example:1) Directive Influence of –OH Group (Hydroxy Group):
OH
I II III
Phenol
Resonance structures of Phenol
Three R.S. place a -ve charge on C-atoms in the ring



:
:
OH
:
OH
:
OH
:
OH
:

Resonance hybrid
OH
Phenol
:
:
- I effect
But -I effect -of OH group is small as compared to
resonance (+R) effect.
LOGO
meta Directing Groups:
Q.1) Explain: Meta directing groups with a suitable example.
(S-04, W-05 &S-06, 1-2 Mark)
Q.2) Define m- directing groups with examples.
(S-11& W-13, 2 Mark)
Q.3) What is meta directing groups? (W-16, 2 Mark)
m- directors:
•meta Directing Groups:
meta-directing groups
or m-directors:
 The group (first substituent) which directs the
second incoming group (i.e. second substituent) to
the meta (m-) position of the aromatic ring or
benzene ring are called meta- directing groups or
m-directors.
meta-directing groups
or m-directors:
meta-directing groups
or m-directors:
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
meta-directing groups
or m-directors:
m-orienting effect of nitro group (-NO2):
Nitrobenzene
strong - I effect & - R effect
- R effect NO2
- I effect
N
I II III
Nitrobenzene
Resonance structures of nitrobenzene


 
Resonance hybrid
O
O
N
O
O
N
O
O
N
O
O
N
O
O
Nitrobenzene


 
Resonance hybrid
N
O
O
+ E
electrophile
NO2
E
meta-substituted product
of nitrobenzene
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
By Dr Pramod R Padole
Problems:
Q.1) Which of the following groups are ortho-para directing and meta-directing. (S-13, 2 Mark)
-COOH, -OH, -CH3, -NH2
Q.2) Predict which of the following groups are o/p directing and m-directing. (S-14, 4 Mark)
-Cl, -COOH, -CH3, -NO2
Q.3) Which of the following groups is o/p directing? (W-14 & W-15, ½ Mark)
a) -NH2b) -NO2 c) -CHO d) –CN
Q.4) Which of the following groups are ortho-para directing and meta-directing. (W-15, 4 Mark)
-COOH, -CH3, -CHO, -OH
Q.5) Nitro group is _______ directing group. (S-16, ½ Mark)
Q.6) Which of the following group is o-p directing group: (W-16, ½ Mark)
(a) -COOH (b) -NH2 (c) -NO2 (d) –CHO
Q.7) Predict the following groups as o/p directing or m-directing: (S-17, 4 Mark)
(i) –Cl (ii) -CHO (iii) -CH3 (iv) –SO3H
Q.8) –NH2 group is _______ directing group. (S-18, ½ Mark)
Q.9) Classify the following groups into ortho-para directing and meta directing group.
(i) –OCH3 (o/p) (ii) -C≡N (m) (iii) -COOH (m) (iv) –CH2Cl (o/p) (S-18, 4 Mark)
Q.10) Classify the following groups into ortho-para directing and meta directing group.
(i) –OH (ii) –COCl (iii) –CH2Cl (iv) –SO3H (S-19, 4 Mark)
Q.11) Which of the following is o/p directing group? (W-19, ½ Mark)
(a) –NH2 (b) –CN (c) –CHO (d) –NO2
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
Activity effect ( or influence):
On the basis of activation & deactivation of the aromatic ring or nucleus by the substituent.
On the basis of activation & deactivation of the aromatic ring or nucleus by the substituent.
Activity effect (or influence):
Activating
groups
Or
Ring
Activators:
Activity Effect
or
Influence:
Deactivating
groups
Or
Ring
De-activators:
Substituents are divided into two types:-
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
By Dr Pramod R Padole
Effect of Substituent groups on further
Electrophilic Substitution:
Directing
(or orienting)
influence
Effect
Of
Substituent
Activity effect
(or influence)
There are two types of influence of substituent's:
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
LOGO
By Dr Pramod R Padole
Activating Groups:
or
Ring Activators:
LOGO
Activating groups or Ring Activators:
 Activating groups or Ring Activators:
 The groups or substituent( first) which increases the rate of second
substitution (reactivity of benzene for further electrophilic substitution) are
called as activating groups or Ring Activators.
 All ortho-para directing groups, except halogens are ring activating groups or
Ring Activators.
The o/p directing groups, except halogens, donate the electrons to benzene ring.
These groups increase the electron density of benzene ring, which makes
the benzene ring more reactive than benzene towards further
electrophilic substitution reaction.
Such groups are called ring activating groups.
Q.1) Explain: Ring Activating Groups with a suitable example (W-04, S-06, W-07, S-08, S-09 & S-16, 2 Mark)
Q.2) What are ring activating groups? Explain with suitable examples. (W-07, W-10 & S-19, 2 Mark)
Q.3) Define: Activating groups with examples. (S-11, S-14 & W-16, 2 Mark)
Q.4) Define with suitable example of Activating group. (W-18 & W-19, 2 Mark)
Examples: O , NH2, NHR, OH, OR, CH3, CH2OH, CH2Cl , C6H5, etc.
..
..
.. .. ..
..
..
..
..
..
..
..:
LOGO
Activating groups or Ring Activators:
LOGO
Deactivating groups :
or Ring De-activators:
Deactivating groups or Ring De-activators:
Deactivating groups or Ring De-activators:
 The groups or substituent (first) which decreases the rate of second
substitution (decreases the reactivity of benzene for further
electrophilic substitution) are called as de-activating groups or
Ring de-activators.
 The meta directing groups along with halogens (it is o/p-directing group)
withdraws electrons from the benzene ring. This decreases the electron
density of the benzene ring, which makes the benzene ring less reactive
than benzene itself, towards further electrophilic substitution reaction.
Hence, these groups are called as ring deactivating groups.
 All meta-directing groups along with halogens are ring deactivating
groups.
 Halogens are o-p directing groups but ring deactivating groups.
Q.1) Explain:- Deactivating Groups with a suitable example. (W-04, S-06, W-07, S-08 & S-09, 1-2 Mark)
Q.2) What are ring deactivating groups? Explain with suitable examples. (W-07, W-10& S-19, 2 Mark)
Q.3) Define with a suitable example: Deactivating Groups. (S-12, S-14, W-16, W-18 & W-19, 2 Mark)
Q.4) Write the structural formula of Benzene sulphonic acid. (S-18, 1 Mark)
Deactivating groups or Ring De-activators:
All meta-directing groups along with halogens are ring deactivating groups.
B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole
LOGO
LOGO
Directive Influence of Halogen, -Cl
( Anomalous behaviour of Halogen):
 Halogens are ortho-para directing, but ring
deactivating groups.
Chlorobenzene
:
Cl
:
:
- I effect is more stronger than + R effect
+ R effect
Cl
I II III
Chlorobenzene
Resonance structures of Chlorobenzene



:
:
Cl:
:
Cl:
:
Cl:
:
Cl:
:

Resonance hybrid
:
LOGO
LOGO
LOGO
www.themegallery.com
(D) Orientation by Dr Pramod R. Padole
Stay Home. Take Care

More Related Content

PPTX
Stereochemistry-Organic Chemistry
PPTX
Electrophillic substitution reaction
PPTX
Heterocyclic aromatic compounds
PDF
Stereochemistry
PPTX
Heterocyclic compounds - Thiophene - Synthesis of Thiophene - Characteristic ...
PPT
Nucleophilic substitution reactions
PPTX
Electrophilic Substitution Reaction in Aromatic Compounds
PPTX
Electrophilic aromatic substitution reactions
Stereochemistry-Organic Chemistry
Electrophillic substitution reaction
Heterocyclic aromatic compounds
Stereochemistry
Heterocyclic compounds - Thiophene - Synthesis of Thiophene - Characteristic ...
Nucleophilic substitution reactions
Electrophilic Substitution Reaction in Aromatic Compounds
Electrophilic aromatic substitution reactions

What's hot (20)

PPTX
UNIT I-PART-3.pptx
PPTX
Diazotisation and coupling reaction
PPTX
Fused heterocyclic compound indole
PPT
2. LiAlH4
PPTX
Birch reduction
PPT
Nomenclature of heterocyclic compound
PPTX
BIRCH REDUCTION_Mechanism and Applications
PPTX
Fused heterocyclic compound isoquinoline
PPTX
E1 MECHANISM priyanka 1.pptx
PPT
Aromaticity
PPTX
Electrophilic substitution reaction.pptx
PPT
Heterocyclic compounds unit III as per PCI syllabus
PPTX
Phenols
PPTX
Indole
PPTX
Improper Rotation
PPTX
Friedel craft reaction
PPTX
stereospecificity and STEREOSELECTIVE.pptx
PPTX
Aromaticity
PPTX
Mesoionic compounds
UNIT I-PART-3.pptx
Diazotisation and coupling reaction
Fused heterocyclic compound indole
2. LiAlH4
Birch reduction
Nomenclature of heterocyclic compound
BIRCH REDUCTION_Mechanism and Applications
Fused heterocyclic compound isoquinoline
E1 MECHANISM priyanka 1.pptx
Aromaticity
Electrophilic substitution reaction.pptx
Heterocyclic compounds unit III as per PCI syllabus
Phenols
Indole
Improper Rotation
Friedel craft reaction
stereospecificity and STEREOSELECTIVE.pptx
Aromaticity
Mesoionic compounds
Ad

Similar to B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole (20)

PDF
Orientation effects_in_substituted_benzenes
PPT
Aromatic substitution for pg
PPTX
Chapter 4 Aromatic Compounds, properties 1.pptx
PPT
Chapter16苯亲电反应
PPTX
PENATARAN LO_Benzene and it_s derivatives.pptx
PPTX
B.Sc. Sem-I Unit-IV Nomenclature and Isomerism of Aromatic Compounds by Dr P...
PPTX
Benzene and its deivatives
PPT
20089_year_one_lectures_wills_220908.ppt
PPTX
Alkyl halide reactions
PPTX
201112_year_one_lectures_wills_for_ajc_with_mw_answers_for_lectures.pptx
PPT
Organic reaction mechanism
PPTX
Topic 3 Introduction to Reaction Mechanism (1).pptx
DOCX
A friedel crafts alkylation love x love begin from here
PPTX
Electrophilic Aromatic Substitution Reaction.pptx
DOCX
Basic principles & questions and answers of organic chemistry
PPTX
Lanthanide shift reagents in nmr
PPTX
B.Sc. Sem-I Unit-IV Aromatic, antiaromatic and non aromatic compounds by Dr P...
PPT
Orientation in Aromatic compounds.ppt
PDF
Halogen compounds 2
PPT
Reaksi sn 1, sn-2, e-1, dan e-2.
Orientation effects_in_substituted_benzenes
Aromatic substitution for pg
Chapter 4 Aromatic Compounds, properties 1.pptx
Chapter16苯亲电反应
PENATARAN LO_Benzene and it_s derivatives.pptx
B.Sc. Sem-I Unit-IV Nomenclature and Isomerism of Aromatic Compounds by Dr P...
Benzene and its deivatives
20089_year_one_lectures_wills_220908.ppt
Alkyl halide reactions
201112_year_one_lectures_wills_for_ajc_with_mw_answers_for_lectures.pptx
Organic reaction mechanism
Topic 3 Introduction to Reaction Mechanism (1).pptx
A friedel crafts alkylation love x love begin from here
Electrophilic Aromatic Substitution Reaction.pptx
Basic principles & questions and answers of organic chemistry
Lanthanide shift reagents in nmr
B.Sc. Sem-I Unit-IV Aromatic, antiaromatic and non aromatic compounds by Dr P...
Orientation in Aromatic compounds.ppt
Halogen compounds 2
Reaksi sn 1, sn-2, e-1, dan e-2.
Ad

More from pramod padole (20)

PPTX
Introduction of Syllabus B. Sc. Part-I (Sem-I) Session-2021-2022 by Dr Pramod...
PPTX
B. Sc. Part - I (Sem-II) Unit-IV (C) Epoxides by Dr Pramod R Padole
PPTX
B.Sc. Part-I (Sem-II) Unit-IV (B) Ethers by Dr Pramod R Padole
PPTX
B. Sc. Part - I (Sem-II) Unit-IV (A) Phenols by Dr Pramod R Padole
PPTX
B.Sc. Sem-II (Unit-III) (C) by Dr Pramod R Padole
PPTX
B.Sc. Sem-II Unit-III (B) Aryl halides by Dr Pramod R Padole
PPTX
B.Sc. (Sem-II) Unit-III (A) Alkenyl Halides by Dr Pramod R Padole
PPTX
Introduction of University Chemistry Syllabus of B. Sc.-Part-I (Sem-II) by Dr...
PPTX
Introduction of Chemistry Syllabus of B. Sc. Part-I (Semester-II) by Dr Pram...
PPTX
Introduction of University Chemistry Syllabus B. Sc.-III (Sem-VI) Session 202...
PPTX
B.Sc. Sem-I Unit-IV Mechanism of electrophilic aromatic substitution by Dr P...
PPTX
Sem - I Unit-III C) Aliphatic Hydrocarbons By Dr Pramod R Padole
PPT
M.Sc.Part-II Sem- III (Unit - IV) Nuclear Magnetic Resonance Spectroscopy
PPTX
Dyes, Drugs & Pesticides by Dr Pramod R Padole
PPTX
Semester - I C) Aliphatic Hydrocarbons by Dr Pramod R Padole
PPTX
Semester - I C) Aliphatic Hydrocarbons by Dr Pramod R Padole
PPTX
Semester - I B) Reactive Intermediates by Dr Pramod R Padole
PPTX
Sem I A) Electronic displacements by Dr Pramod R Padole
PPTX
Heterocyclic Compounds Part -III (Pyrrole) by Dr Pramod R Padole
PPTX
Heterocyclic Compounds Part-II (Pyrrole) by Dr Pramod R Padole
Introduction of Syllabus B. Sc. Part-I (Sem-I) Session-2021-2022 by Dr Pramod...
B. Sc. Part - I (Sem-II) Unit-IV (C) Epoxides by Dr Pramod R Padole
B.Sc. Part-I (Sem-II) Unit-IV (B) Ethers by Dr Pramod R Padole
B. Sc. Part - I (Sem-II) Unit-IV (A) Phenols by Dr Pramod R Padole
B.Sc. Sem-II (Unit-III) (C) by Dr Pramod R Padole
B.Sc. Sem-II Unit-III (B) Aryl halides by Dr Pramod R Padole
B.Sc. (Sem-II) Unit-III (A) Alkenyl Halides by Dr Pramod R Padole
Introduction of University Chemistry Syllabus of B. Sc.-Part-I (Sem-II) by Dr...
Introduction of Chemistry Syllabus of B. Sc. Part-I (Semester-II) by Dr Pram...
Introduction of University Chemistry Syllabus B. Sc.-III (Sem-VI) Session 202...
B.Sc. Sem-I Unit-IV Mechanism of electrophilic aromatic substitution by Dr P...
Sem - I Unit-III C) Aliphatic Hydrocarbons By Dr Pramod R Padole
M.Sc.Part-II Sem- III (Unit - IV) Nuclear Magnetic Resonance Spectroscopy
Dyes, Drugs & Pesticides by Dr Pramod R Padole
Semester - I C) Aliphatic Hydrocarbons by Dr Pramod R Padole
Semester - I C) Aliphatic Hydrocarbons by Dr Pramod R Padole
Semester - I B) Reactive Intermediates by Dr Pramod R Padole
Sem I A) Electronic displacements by Dr Pramod R Padole
Heterocyclic Compounds Part -III (Pyrrole) by Dr Pramod R Padole
Heterocyclic Compounds Part-II (Pyrrole) by Dr Pramod R Padole

Recently uploaded (20)

PDF
GROUP 2 ORIGINAL PPT. pdf Hhfiwhwifhww0ojuwoadwsfjofjwsofjw
PDF
7.Physics_8_WBS_Electricity.pdfXFGXFDHFHG
PPTX
HAEMATOLOGICAL DISEASES lack of red blood cells, which carry oxygen throughou...
PPTX
perinatal infections 2-171220190027.pptx
PPTX
PMR- PPT.pptx for students and doctors tt
PPT
1. INTRODUCTION TO EPIDEMIOLOGY.pptx for community medicine
PPTX
Cells and Organs of the Immune System (Unit-2) - Majesh Sir.pptx
PPTX
Substance Disorders- part different drugs change body
PPTX
Introcution to Microbes Burton's Biology for the Health
PDF
Worlds Next Door: A Candidate Giant Planet Imaged in the Habitable Zone of ↵ ...
PPTX
GREEN FIELDS SCHOOL PPT ON HOLIDAY HOMEWORK
PPT
Biochemestry- PPT ON Protein,Nitrogenous constituents of Urine, Blood, their ...
PDF
Communicating Health Policies to Diverse Populations (www.kiu.ac.ug)
PPT
LEC Synthetic Biology and its application.ppt
PDF
CuO Nps photocatalysts 15156456551564161
PPTX
Understanding the Circulatory System……..
PDF
Social preventive and pharmacy. Pdf
PDF
Chapter 3 - Human Development Poweroint presentation
PPTX
2currentelectricity1-201006102815 (1).pptx
PDF
Integrative Oncology: Merging Conventional and Alternative Approaches (www.k...
GROUP 2 ORIGINAL PPT. pdf Hhfiwhwifhww0ojuwoadwsfjofjwsofjw
7.Physics_8_WBS_Electricity.pdfXFGXFDHFHG
HAEMATOLOGICAL DISEASES lack of red blood cells, which carry oxygen throughou...
perinatal infections 2-171220190027.pptx
PMR- PPT.pptx for students and doctors tt
1. INTRODUCTION TO EPIDEMIOLOGY.pptx for community medicine
Cells and Organs of the Immune System (Unit-2) - Majesh Sir.pptx
Substance Disorders- part different drugs change body
Introcution to Microbes Burton's Biology for the Health
Worlds Next Door: A Candidate Giant Planet Imaged in the Habitable Zone of ↵ ...
GREEN FIELDS SCHOOL PPT ON HOLIDAY HOMEWORK
Biochemestry- PPT ON Protein,Nitrogenous constituents of Urine, Blood, their ...
Communicating Health Policies to Diverse Populations (www.kiu.ac.ug)
LEC Synthetic Biology and its application.ppt
CuO Nps photocatalysts 15156456551564161
Understanding the Circulatory System……..
Social preventive and pharmacy. Pdf
Chapter 3 - Human Development Poweroint presentation
2currentelectricity1-201006102815 (1).pptx
Integrative Oncology: Merging Conventional and Alternative Approaches (www.k...

B. Sc. Sem - I Unit-IV (D) Orientation by Dr Pramod R Padole

  • 1. 1 B.Sc. First year Students Semester – I Unit-IV (D) Orientation by Dr Pramod R Padole
  • 2. 2
  • 4. Unit IV- Aromatic Hydrocarbons Orientation: Effect of substituent groups. Activating and deactivating groups. Theory of reactivity and orientation on the basis of inductive and resonance effects (-CH3, -OH, -NO2 and –Cl groups). D Nomenclature and Isomerism of Aromatic Compounds: Structure of Benzene: Kekule structure and Molecular orbital structure. A Aromaticity and Huckel’s rule Aromatic, antiaromatic and non-aromatic systems B Mechanism of Electrophilic Aromatic Substitution: Nitration, Friedal Craft Alkylation and Acylation.Nuclear and Side Chain Halogination, Birch Reduction C
  • 5. LOGO D) Orientation: The process of determine the position of substituent in the substituted benzene is called orientation. Or The relative arrangement of atoms or groups on the aromatic ring is called orientation.
  • 6. By Dr Pramod R Padole Orientation: Defination: The process of determine the position of substituent in the substituted benzene is called orientation. Or Defination: The relative arrangement of atoms or groups on the aromatic ring is called orientation.  The new group is located either ortho, meta or para positions to the existing substituent (first/original).  The identity of the first substituent determines the position of the second substituent.  Substitution in Mono-substituted Benzene:
  • 7. By Dr Pramod R Padole Effect of Substituent groups on further Electrophilic Substitution: Directing (or orienting) influence Effect Of Substituent Activity effect (or influence) There are two types of influence of substituent's:
  • 8. Directing (or orienting) influence: Substituent group, X, directs the incoming group, Y, either to ortho and para positions or only to m-position.  This effect of group already present (-X) on the benzene ring is known as orienting (directive) influence of the group or orientation effect.
  • 9. pramodpadole@gmail.com By Dr Pramod R Padole Directing (or orienting) influence: Ortho-Para (o/p) Directing Groups: or o-p directors: Directing (Orienting) influence meta (m) Directing Groups: or m directors: The substituent groups are thus classified into two types.
  • 10. Ortho-para directing groups or o-p directors: Ortho-para directing groups or o-p directors: The group (first substituent) which directs the second incoming group (i.e. second substituent) to the ortho-para (o-p) positions of the aromatic ring or benzene ring simultaneously are called ortho-para directing groups or o-p directors. Q.1) Explain: Ortho-Para directing groups with a suitable example. (S-04, W-05 & S-06, 2 Mark) Q.2) Define with a suitable example: Ortho-Para directing groups. (S-12 & W-13, 2 Mark)
  • 11. Ortho-para directing groups or o-p directors:
  • 12. Ortho-para directing groups or o-p directors:
  • 14. Ortho-para directing groups or o-p directors: CH3 Toluene + I effect
  • 15. Ortho-para directing groups or o-p directors: Directive influence of o, p-directing groups:  Example:1) Directive Influence of –OH Group (Hydroxy Group): OH I II III Phenol Resonance structures of Phenol Three R.S. place a -ve charge on C-atoms in the ring    : : OH : OH : OH : OH :  Resonance hybrid OH Phenol : : - I effect But -I effect -of OH group is small as compared to resonance (+R) effect.
  • 16. LOGO meta Directing Groups: Q.1) Explain: Meta directing groups with a suitable example. (S-04, W-05 &S-06, 1-2 Mark) Q.2) Define m- directing groups with examples. (S-11& W-13, 2 Mark) Q.3) What is meta directing groups? (W-16, 2 Mark) m- directors: •meta Directing Groups:
  • 17. meta-directing groups or m-directors:  The group (first substituent) which directs the second incoming group (i.e. second substituent) to the meta (m-) position of the aromatic ring or benzene ring are called meta- directing groups or m-directors.
  • 21. meta-directing groups or m-directors: m-orienting effect of nitro group (-NO2): Nitrobenzene strong - I effect & - R effect - R effect NO2 - I effect N I II III Nitrobenzene Resonance structures of nitrobenzene     Resonance hybrid O O N O O N O O N O O N O O Nitrobenzene     Resonance hybrid N O O + E electrophile NO2 E meta-substituted product of nitrobenzene
  • 23. By Dr Pramod R Padole Problems: Q.1) Which of the following groups are ortho-para directing and meta-directing. (S-13, 2 Mark) -COOH, -OH, -CH3, -NH2 Q.2) Predict which of the following groups are o/p directing and m-directing. (S-14, 4 Mark) -Cl, -COOH, -CH3, -NO2 Q.3) Which of the following groups is o/p directing? (W-14 & W-15, ½ Mark) a) -NH2b) -NO2 c) -CHO d) –CN Q.4) Which of the following groups are ortho-para directing and meta-directing. (W-15, 4 Mark) -COOH, -CH3, -CHO, -OH Q.5) Nitro group is _______ directing group. (S-16, ½ Mark) Q.6) Which of the following group is o-p directing group: (W-16, ½ Mark) (a) -COOH (b) -NH2 (c) -NO2 (d) –CHO Q.7) Predict the following groups as o/p directing or m-directing: (S-17, 4 Mark) (i) –Cl (ii) -CHO (iii) -CH3 (iv) –SO3H Q.8) –NH2 group is _______ directing group. (S-18, ½ Mark) Q.9) Classify the following groups into ortho-para directing and meta directing group. (i) –OCH3 (o/p) (ii) -C≡N (m) (iii) -COOH (m) (iv) –CH2Cl (o/p) (S-18, 4 Mark) Q.10) Classify the following groups into ortho-para directing and meta directing group. (i) –OH (ii) –COCl (iii) –CH2Cl (iv) –SO3H (S-19, 4 Mark) Q.11) Which of the following is o/p directing group? (W-19, ½ Mark) (a) –NH2 (b) –CN (c) –CHO (d) –NO2
  • 25. Activity effect ( or influence): On the basis of activation & deactivation of the aromatic ring or nucleus by the substituent.
  • 26. On the basis of activation & deactivation of the aromatic ring or nucleus by the substituent. Activity effect (or influence): Activating groups Or Ring Activators: Activity Effect or Influence: Deactivating groups Or Ring De-activators: Substituents are divided into two types:-
  • 28. By Dr Pramod R Padole Effect of Substituent groups on further Electrophilic Substitution: Directing (or orienting) influence Effect Of Substituent Activity effect (or influence) There are two types of influence of substituent's:
  • 38. LOGO By Dr Pramod R Padole Activating Groups: or Ring Activators:
  • 39. LOGO Activating groups or Ring Activators:  Activating groups or Ring Activators:  The groups or substituent( first) which increases the rate of second substitution (reactivity of benzene for further electrophilic substitution) are called as activating groups or Ring Activators.  All ortho-para directing groups, except halogens are ring activating groups or Ring Activators. The o/p directing groups, except halogens, donate the electrons to benzene ring. These groups increase the electron density of benzene ring, which makes the benzene ring more reactive than benzene towards further electrophilic substitution reaction. Such groups are called ring activating groups. Q.1) Explain: Ring Activating Groups with a suitable example (W-04, S-06, W-07, S-08, S-09 & S-16, 2 Mark) Q.2) What are ring activating groups? Explain with suitable examples. (W-07, W-10 & S-19, 2 Mark) Q.3) Define: Activating groups with examples. (S-11, S-14 & W-16, 2 Mark) Q.4) Define with suitable example of Activating group. (W-18 & W-19, 2 Mark) Examples: O , NH2, NHR, OH, OR, CH3, CH2OH, CH2Cl , C6H5, etc. .. .. .. .. .. .. .. .. .. .. .. ..:
  • 40. LOGO Activating groups or Ring Activators:
  • 41. LOGO Deactivating groups : or Ring De-activators:
  • 42. Deactivating groups or Ring De-activators: Deactivating groups or Ring De-activators:  The groups or substituent (first) which decreases the rate of second substitution (decreases the reactivity of benzene for further electrophilic substitution) are called as de-activating groups or Ring de-activators.  The meta directing groups along with halogens (it is o/p-directing group) withdraws electrons from the benzene ring. This decreases the electron density of the benzene ring, which makes the benzene ring less reactive than benzene itself, towards further electrophilic substitution reaction. Hence, these groups are called as ring deactivating groups.  All meta-directing groups along with halogens are ring deactivating groups.  Halogens are o-p directing groups but ring deactivating groups. Q.1) Explain:- Deactivating Groups with a suitable example. (W-04, S-06, W-07, S-08 & S-09, 1-2 Mark) Q.2) What are ring deactivating groups? Explain with suitable examples. (W-07, W-10& S-19, 2 Mark) Q.3) Define with a suitable example: Deactivating Groups. (S-12, S-14, W-16, W-18 & W-19, 2 Mark) Q.4) Write the structural formula of Benzene sulphonic acid. (S-18, 1 Mark)
  • 43. Deactivating groups or Ring De-activators: All meta-directing groups along with halogens are ring deactivating groups.
  • 45. LOGO
  • 46. LOGO Directive Influence of Halogen, -Cl ( Anomalous behaviour of Halogen):  Halogens are ortho-para directing, but ring deactivating groups. Chlorobenzene : Cl : : - I effect is more stronger than + R effect + R effect Cl I II III Chlorobenzene Resonance structures of Chlorobenzene    : : Cl: : Cl: : Cl: : Cl: :  Resonance hybrid :
  • 47. LOGO
  • 48. LOGO
  • 49. LOGO www.themegallery.com (D) Orientation by Dr Pramod R. Padole Stay Home. Take Care