Iductive effect
INDUCTIVE EFFECT
The polarization of a bond induced by an adjacent polar bond through movement of sigma electrons is called inductive effect.
Reason:
The inductive effect refers to the polarity produced in a molecule as a result of higher electronegativity of one atom as compared to another.
ʆʆ+ ʆ+ ʆ-
CH3CH2Cl
Chloroethane
Another example is of ethyle trialkyle ammonium cation.
ʆʆ + ʆ+ +
CH3 CH2 NR3
Inductive effect can operate in opposite direction depending upon nature of functional groups.For example
ʆʆ- ʆ- -
CH3 CH2 O
The functional groups responsible for producing inductive effect can be classified as
1.Electron withdrawing groups (-I)
2.Electron donating groups (+I)
Course Material
- Resonance
- Resonance Effect
- Dipole Moment
- Iductive effect
- Hydrogen Bonding
- Nomenclature of Organic Compounds
- Alkanes and Cycloalkanes
- Alkenes and Alkynes
- Wittig Reaction
- Isomerism
- Isomerism I
- optical isomerism
- Aromatic Electrophilic Substitution Reactions
- Nucleophilic Substitution Reactions I
- Nucleophilic Substitution Reactions II
- Nucleophilic Substitution Reactions III
- Alcohols 1
- Alcohols 2
- Carboxylic Acid 1
- Carboxylic Acid 2
- Aldehyde and ketone
- Base catalyzed reactions of carbonyl compounds I
- Base catalyzed reactions of carbonyl compounds II
- Aldol Condensation
- Reactions of alkyl amines, Arene diazonium salts
- Unsaturated Hydrocarbons
- Chapters 26
- Department Biotechnology
- Teacher
Dr. Syed Gohar Taqi Kazimi