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primary

Stericlly hindered. primary. SN2 or E2. Strong nucleophile. primary. SN2 or E2. Strong base. diahlide. Double E2. Stericlly hindered. primary. SN2 or E2. Stericlly hindered. secondary. major. SN1, E!, SN2 or E2. Weak base. tertiary. SN1. No SN2. E1. Strong base. dihalide.

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primary

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  1. Stericlly hindered primary SN2 or E2

  2. Strong nucleophile primary SN2 or E2

  3. Strong base diahlide Double E2

  4. Stericlly hindered primary SN2 or E2

  5. Stericlly hindered secondary major SN1, E!, SN2 or E2

  6. Weak base tertiary SN1 No SN2 E1

  7. Strong base dihalide Double E2

  8. dihalide Strong base Double E2

  9. Weak base secondary E1 SN1 SN1, E!, SN2 or E2

  10. Weak base SN1 tertiary SN1, E!, SN2 or E2 E1

  11. Constitutional isomers stereoisomers

  12. Not isomers Identical, achiral

  13. Identical, achiral 4 different groups, chiral

  14. R S R identical eantiomers S enantiomers

  15. (4R,5S)-4,5-diethyloctane R (3R)-3-methylhexane R S

  16. R R R (3R,5R,6R)-5-ethyl-3,6-dimethylnonane

  17. enantiomers S,R A R,S diastereomers B RR

  18. A enantiomers S,S R,R B S,R diastereomers

  19. A S,R R,S enantiomers B R,R diastereomers

  20. A R,R S,R diastereomers B diastereomers R,S

  21. diastereomers diastereomers

  22. Optically active? C and D same boiling point? C and D An equal mixture of B and C would be? Optically active

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