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Old March 2nd, 2005, 19:25
al al is offline
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Default (2S,3S)-3-bromo-2-methoxybutane undergoes an Sn2 reaction
When (2S,3S)-3-bromo-2-methoxybutane undergoes an Sn2 reaction with methoxide ion, the product is not optically active. Why is that??
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Old March 3rd, 2005, 04:09
RobJim RobJim is offline
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Well, the methoxy ion, CH3O(-), will perform a backside attack on carbon-3, displacing the bromine. This will form a substance identical to it's enantiomer. What is that molecule?
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