`Di-t-`butyl ether is prepared best by the reaction

Assertion: t-Butyl methyl ether is not prepared by the reaction of t-butyl bromide with sodium methoxide. Reason: Sodium methoxide is a strong nucleophile.

Assertion. t -Butyl Methyl ether is not prepared by the reaction of t- butyl bromide with sodium methoxide. Reason: Sodium methoxide is a strong nucleophile.

Ethers can be prepared by Williamson synthesis which an alkyl halide is reacted with sodium alkoxide. Di-tert-butyl ether can't be prepared by this method. Explain.

Ethers can be prepared by Williamson synthesis which an alkyl halide is reacted with sodium alkoxide. Di-tert-butyl ether can't be prepared by this method. Explain.

Ethers can be prepared by Williamson synthesis in which an alkyl halide is reacted with sodium alkoxide. Di-tert-buty ether can't be prepared by this method. Explain