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Topic: hydride nucleophiles reactivity  (Read 2448 times)

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Offline marky02

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hydride nucleophiles reactivity
« on: April 25, 2010, 05:02:03 PM »
hi,have a reactivity question

why would Cyclohexanone be approximately 10 times more reactive toward hydride nucleophiles than cyclohexenone?
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Offline MissPhosgene

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Re: hydride nucleophiles reactivity
« Reply #1 on: April 25, 2010, 09:03:05 PM »
What type of stabilization does cyclohexenone have that cyclohexanone doesn't?
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Stereograms of the 32 crystallographic point groups: little bike wheels of cold, hard, pure rationality.
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