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Williamson synthesis of ether is an example of
- a)Nucleophilic addition
- b)Electrophilic substitution
- c)Nucleophilic substitution
- d)Electrophilic addition
Correct answer is option 'C'. Can you explain this answer?
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Williamson synthesis of ether is an example ofa)Nucleophilic additionb...
Williamson synthesis of ether is an SN^2 reaction with an alkoxide ion as the nucleophile.The reaction takes place by the substitution of halide from alkyl halide by the alkoxide ion.Hence it is a nucleophilic substitution reaction which is followed by inversion of configuration at the Chiral centre.
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Williamson synthesis of ether is an example ofa)Nucleophilic additionb...
Williamson synthesis of ether
Ether is synthesized by the Williamson synthesis method, which involves the reaction between an alkyl halide and a deprotonated alcohol. This reaction is an example of nucleophilic substitution.
Nucleophilic substitution
- In the Williamson synthesis, the alkoxide ion acts as the nucleophile, attacking the electrophilic carbon of the alkyl halide.
- The nucleophile replaces the halogen atom, resulting in the formation of an ether molecule.
- This reaction follows the SN2 mechanism, where the alkoxide ion directly displaces the leaving group.
Key points:
- The Williamson synthesis is a widely used method for the synthesis of ethers in organic chemistry.
- Nucleophilic substitution reactions involve the attack of a nucleophile on an electrophilic carbon atom.
- In this reaction, the alkoxide ion acts as the nucleophile, displacing the halogen atom in the alkyl halide.
- The formation of ether through the Williamson synthesis is a classic example of nucleophilic substitution in organic chemistry.
Ether is synthesized by the Williamson synthesis method, which involves the reaction between an alkyl halide and a deprotonated alcohol. This reaction is an example of nucleophilic substitution.
Nucleophilic substitution
- In the Williamson synthesis, the alkoxide ion acts as the nucleophile, attacking the electrophilic carbon of the alkyl halide.
- The nucleophile replaces the halogen atom, resulting in the formation of an ether molecule.
- This reaction follows the SN2 mechanism, where the alkoxide ion directly displaces the leaving group.
Key points:
- The Williamson synthesis is a widely used method for the synthesis of ethers in organic chemistry.
- Nucleophilic substitution reactions involve the attack of a nucleophile on an electrophilic carbon atom.
- In this reaction, the alkoxide ion acts as the nucleophile, displacing the halogen atom in the alkyl halide.
- The formation of ether through the Williamson synthesis is a classic example of nucleophilic substitution in organic chemistry.
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Williamson synthesis of ether is an example ofa)Nucleophilic additionb)Electrophilic substitutionc)Nucleophilic substitutiond)Electrophilic additionCorrect answer is option 'C'. Can you explain this answer?
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