Why does the carbocation intermediate in the hydrolysis of 2-bromo-3-methylbutane rearrange by way of a hydride shift rather than a methyl shift? Diethyl ether (CH3CH2OCH2CH3) has a dielectric constant of 4. What best describes its solvent properties: polar protic, nonpolar protic, polar aprotic, or nonpolar aprotic?
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Ineed to find the answer of this question because i dont understand it
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Why does the carbocation intermediate in the hydrolysis of 2-bromo-3-methylbutane rearrange by way o...
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