Answer:
In the acid-catalyzed dehydration of 2-methyl-2-butanol, the reaction can be driven to completion using Le Chatelier's principle. The reaction is driven to completion because the released water molecules form a strong bond with the acid used as a catalyst. As a result, the alkene produced can be distilled from the mixture.
Explanation:
In the acid-catalyzed dehydration of 2-methyl-2-butanol, the reaction can be driven to completion using Le Chatelier's principle. The reaction is driven to completion because the released water molecules form a strong bond with the acid used as a catalyst. As a result, the alkene produced can be distilled from the mixture.
In the acid-catalyzed dehydration of 2-methyl-2-butanol, the response may be pushed to of of entirety the usage of Le Ch-atelier's principle. The response is pushed to of of entirety due to the fact the launched water molecules shape a robust bond with the acid used as a catalyst. As a result, the alkene produced may be distilled from the mixture.
The acid-catalyzed dehydration of secondary and tertiary alcohols proceeds through an E1 mechanism. First, the hydroxyl institution within side the alcohol is protonated in a quick step to shape an alkyloxonium ion. Next, a molecule of water is misplaced from the alkyloxonium ion within side the slow, rate-figuring out step, leaving in the back of a carbocation.
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