preparation of Tert butyl methyl ether via Williamson synthesis
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The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide). The correct pair of reactants used for the preparation of tert-butyl ethyl ether are sodium tert-butoxide and ethyl bromide.
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide). The correct pair of reactants used for the preparation of tert-butyl ethyl ether are sodium tert-butoxide and ethyl bromide. Williamson reaction: R−O
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide). The correct pair of reactants used for the preparation of tert-butyl ethyl ether are sodium tert-butoxide and ethyl bromide. Williamson reaction: R−O −
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide). The correct pair of reactants used for the preparation of tert-butyl ethyl ether are sodium tert-butoxide and ethyl bromide. Williamson reaction: R−O − +R
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide). The correct pair of reactants used for the preparation of tert-butyl ethyl ether are sodium tert-butoxide and ethyl bromide. Williamson reaction: R−O − +R ′
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide). The correct pair of reactants used for the preparation of tert-butyl ethyl ether are sodium tert-butoxide and ethyl bromide. Williamson reaction: R−O − +R ′
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide). The correct pair of reactants used for the preparation of tert-butyl ethyl ether are sodium tert-butoxide and ethyl bromide. Williamson reaction: R−O − +R ′ −X⟶R−O−R
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide). The correct pair of reactants used for the preparation of tert-butyl ethyl ether are sodium tert-butoxide and ethyl bromide. Williamson reaction: R−O − +R ′ −X⟶R−O−R ′
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide). The correct pair of reactants used for the preparation of tert-butyl ethyl ether are sodium tert-butoxide and ethyl bromide. Williamson reaction: R−O − +R ′ −X⟶R−O−R ′
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide). The correct pair of reactants used for the preparation of tert-butyl ethyl ether are sodium tert-butoxide and ethyl bromide. Williamson reaction: R−O − +R ′ −X⟶R−O−R ′ +X
The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol (alkoxide). The correct pair of reactants used for the preparation of tert-butyl ethyl ether are sodium tert-butoxide and ethyl bromide. Williamson reaction: R−O − +R ′ −X⟶R−O−R ′ +X −
Explanation:
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