Which from following is a suitable method for preparation of ether?
Show Hint
- Reacting sodium methoxide and tertiary butyl bromide
- Reacting sodium tertiarybutoxide and methyl bromide
- Reacting methyl alcohol and ethene
- Reacting methyl alcohol and methyl bromide
The Correct Option is B
Solution and Explanation
To make a hindered ether, put the bulky group on the alkoxide and the small group on the halide. So t-BuONa + CH$_3$Br. Option (B).
Final Answer:
Option (B). \[ \boxed{\text{(B)}} \]
Top Questions on Ethers
IUPAC name of the given ether is:
- MHT CET - 2024
- Chemistry
- Ethers
Replacement of a hydrogen atom in a hydrocarbon by an alkoxy or carboxyl group yields a class of compounds known as ethers. Ethers are classified as symmetrical or unsymmetrical on the basis of groups attached to the oxygen atoms. Diethyl ether, a symmetrical ether, has been widely used as an inhalation anesthetic. Ethers can be prepared by acid catalyzed intermolecular dehydration of alcohols and Williamson's synthesis. Acid catalyzed dehydration of alcohols is not generally preferred as it gives a mixture of elimination and substitution products. In Williamson's synthesis, an alkyl halide is allowed to react with sodium alkoxide. Ethers containing substituted Alkyl groups may also be prepared by this method. The C-O bond in ether is weakly polar and is cleaved under drastic conditions with excess of hydrogen halides. In electrophilic substitution, the alkoxy group deactivates the aromatic ring and directs the incoming group to ortho and para positions.
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(A) Br\(_2\)/FeBr\(_3\)
(B) Mg, dry Ether
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(D) Methanol, Conc. H\(_2\)SO\(_4\) - What happens when C₆H₅–O–R is treated with HX?
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