Explain why 1-methylaziridine undergoes amine inversion much more slowly than 1-methylpyrrolidine. (What are the hybridization and bond
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Explain why 1-methylaziridine undergoes amine inversion much more slowly than 1-methylpyrrolidine. (What are the hybridization and bond angles at nitrogen in the transition state for inversion?)
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N-CH3 :N-CH3 1-methylaziridine 1-methylpyrrolidine
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In the transition state for inversion of both amines the nitrogen is sphybridized The CNC ang...View the full answer
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