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Quinuclidine reacts faster with isopropyl chloride in an SN2 reaction than triethylamine due to its increased nucleophilicity and steric hindrance. The nitrogen atom in quinuclidine is more basic and thus a stronger nucleophile compared to triethylamine, leading to a faster reaction rate. Additionally, the compact structure of quinuclidine reduces steric hindrance, allowing for better approach of the nucleophile to the substrate in the SN2 reaction.

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1y ago

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