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Explain Carbocation
The mechanism is a sequence of two Brønsted acid-base reactions. In the first (step a), the double bond is protonated to give a tertiary carbocation; in the second (step b), the carbocation loses a dissimilar proton to give the alkene. The equilibrium is driven to the right by the greater stability of the alkene product. (Why is it more stable?)
What is linear geometry The beryllium (Be) bears two groups, and thus has linear geometry. The H-Be-H bond angle is 180°.
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