NUCLEOPHILIC ADDITION REACTION

 
   NUCLEOPHILIC ADDITION REACTION
 Addition reaction occurs when 2 or more reactants  combine together
to form products withoutl9oss of any atoms present in the reactants
 CHO/ C=O Groups highly polar in nature
 The positively charged carbon atom   readily attacked by  electron
rich nucleophile (Nu-),
 The negatively charged oxygen attacked by electron deficient
electrophile (E+)
In this reaction:
First Step:  T
he positively  carbon atom attacked by nucleophile  to
form new Pi bond between C-O is  broken, the pai of electron  goes to
oxygen which acquire negative charge
Second Step
: The electrophile  (example: H+) Attack to the negatively
charged oxygen to form addition product
 
                    MECHANISM
 
   
BASE/ ACID CATALYSED  ADDITION REACTION
 
1. Base catalyzed:
 
The  Base convert a weak nucleophile to a strong one by removing a
proton (H+)
 
The strong nucleophile then add the carbonyl group
 
               Nu-H  + B ------------NU:-    + BH+
 
              (weak neutral)     (anionic-strong)
 
2. Acid catalyzed 
:
 
Hydrogen from the acid attack negatively charged  carbonyl oxygen
to give protonated carbonyl group. This is resonance stabilized
 
(NOTE) -Addition product is same in both the cases;
 
           - C=O Group is less reactive than -CHO
 
            ELECTROMERIC EFFECT
 Electromeric effect are electronic factors that influence chemical
reactions of organic compounds.
 Electromeric effect is the complete transfer of pi electrons in a
molecule in the presence of an attacking agent.
 E
lectromeric effect can be observed in Pi bonds
 Electromeric effect occurs when a molecule having multiple bonds is
exposed to an attacking agent such as a proton (H
+
).
Types:
 
 
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Nucleophilic addition reactions involve the combination of two or more reactants resulting in the formation of products without loss of atoms. This reaction is guided by the highly polar nature of CHO/C=O groups. The mechanism consists of steps where nucleophiles attack positively charged carbon atoms while electrophiles target negatively charged oxygens. Additionally, the role of base and acid catalysis in such reactions is discussed, along with the concept of electromeric effect in influencing organic compound reactions.

  • Nucleophilic Addition
  • Reaction Mechanism
  • Organic Chemistry
  • Electromeric Effect

Uploaded on Feb 17, 2025 | 0 Views


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  1. NUCLEOPHILIC ADDITION REACTION Addition reaction occurs when 2 or more reactants combine together to form products withoutl9oss of any atoms present in the reactants CHO/ C=O Groups highly polar in nature The positively charged carbon atom readily attacked by electron rich nucleophile (Nu-), The negatively charged oxygen attacked by electron deficient electrophile (E+) In this reaction: First Step: The positively carbon atom attacked by nucleophile to form new Pi bond between C-O is broken, the pai of electron goes to oxygen which acquire negative charge Second Step: The electrophile (example: H+) Attack to the negatively charged oxygen to form addition product

  2. MECHANISM

  3. BASE/ ACID CATALYSED ADDITION REACTION 1. Base catalyzed: The Base convert a weak nucleophile to a strong one by removing a proton (H+) The strong nucleophile then add the carbonyl group Nu-H + B ------------NU:- + BH+ (weak neutral) (anionic-strong) 2. Acid catalyzed : Hydrogen from the acid attack negatively charged carbonyl oxygen to give protonated carbonyl group. This is resonance stabilized (NOTE) -Addition product is same in both the cases; - C=O Group is less reactive than -CHO

  4. ELECTROMERIC EFFECT Electromeric effect are electronic factors that influence chemical reactions of organic compounds. Electromeric effect is the complete transfer of pi electrons in a molecule in the presence of an attacking agent. Electromeric effect can be observed in Pi bonds Electromeric effect occurs when a molecule having multiple bonds is exposed to an attacking agent such as a proton (H+). Types:

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