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NEIGHBORING GROUP PARTICIPATION

NEIGHBORING GROUP PARTICIPATION. WHEN YOU NEIGHBOR HELPS OUT. a -Bromopropionate Ion. -. -. S N 2. -. neither S N 1 or S N 2. Two different results!. REACTION IN CONCENTRATED BASE. straightforward S N 2 displacement. S N 2 ( rate = k[RBr] [OH] ) is favored by high [OH].

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NEIGHBORING GROUP PARTICIPATION

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  1. NEIGHBORING GROUP PARTICIPATION WHEN YOU NEIGHBOR HELPS OUT

  2. a-Bromopropionate Ion - - SN2 - neither SN1 or SN2 Two different results!

  3. REACTION IN CONCENTRATED BASE straightforward SN2 displacement SN2 ( rate = k[RBr] [OH] ) is favored by high [OH]

  4. REACTION IN DILUTE BASE neighboring group participation In dilute base the internal displacement has a competing rate. Two inversions give a product with retention.

  5. SOLVOLYSIS OF BROSYLATES

  6. PREPARING A BROSYLATE LEAVING GROUP p-bromobenzenesulfonyl chloride Brosyl Chloride BsCl resonance stabilized good leaving group a brosylate (R-OBs)

  7. THE METHYL BROSYLATE GIVES 50/50 CIS + TRANS + SN1

  8. THE ACETOXY BROSYLATE GIVES 100% TRANS

  9. INTERMEDIATE ION Bridged ion, OAc attacks equally on either side, but always anti + + - O-Ac trans diacetate

  10. REARRANGEMENTS CAN ASSIST A REACTION ALSO To be added …...

  11. NGP IS COMMON IN BIOLOGICAL REACTIONS

  12. AN IMPORTANT BIOLOGICAL REACTION IN THE SYNTHESIS OF TERPENES isopentenyl pyrophosphate TERPENES ENZYME 3,3-dimethylallyl pyrophosphate USES NEIGHBORING GROUP PARTICIPATION

  13. SOME TERPENES (C10) geraniol menthol rose and other flowers peppermint camphor a-pinene camphor tree turpentine

  14. ANCHIMERIC ASSISTANCE BY HISTIDINE good nucleophile assisted by proximity + ENZYMES KNOW ALL THE TRICKS : SN2 - - enzyme double bond could never displace without the imidizole trick easily displaced weak base SN2 + elimination :B

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