| 1. | Typically, electron deficient olefins are oxidized more slowly than electron rich ones.
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| 2. | The 5-position is less electron deficient and substitutents there are quite stable.
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| 3. | Following this transfer event, the electron deficient anion undergoes internal rearrangement and fragments.
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| 4. | One method for palladium-catalyzed cross-coupling reactions of electron deficient arene.
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| 5. | The classical Ullmann reaction is limited to electron deficient aryl halides and requires harsh reaction conditions.
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| 6. | In organic solution the electron deficient self-assemble by formation of a charge transfer complex.
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| 7. | C 60 behaves very much like an electron deficient alkene and readily reacts with electron rich species.
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| 8. | Then, followed by intramolecular nucleophilic substitution, the second hydroxyl group attacks the electron deficient carbon.
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| 9. | Metal atoms contain few electrons in their electron deficient elements and the communal sharing does not change that.
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| 10. | The metal complex must be electron deficient in nature, allowing it to accept electrons from the superoxide.
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