Across
- 2. term that dominates in hydration
- 6. these electrons are lower in energy
- 7. what can happen in electrophilic addition due to the carbocation intermediate
- 9. one of two things set during the first step on the way to converting an alkene to an anti-Markovnikov alcohol
- 15. what is needed for free radical hydrohalogenation
- 20. what vicinal dihalide involves
- 21. the reverse of E1
- 22. term that dominates in dehydration
- 23. what is added first to the alkene to yield the anti-Markovnikov alkyl halide
- 24. the nucleophile in hydration
- 25. part the hydronium ion plays in the electrophilic addition of an alkene
Down
- 1. the final step in converting an alkene to an anti-Markovnikov alcohol
- 3. the first step to making an anti-Markovnikov alcohol from an alkene
- 4. what is added first in electrophilic addition to yield the Markovnikov alkyl halide
- 5. a description for the cyclic bromonium ion
- 8. needed for practical hydrogenation rates
- 10. the aspect of the reaction that Markovnikov’s rule describes
- 11. what dehydrohalogenation is
- 12. one of two things set during the first step on the way to converting an alkene to an anti-Markovnikov alcohol.
- 13. what hydrogenation reactions are
- 14. what hydrogenation involves
- 16. how the BH2 and H are added to the carbons of an alkene
- 17. what you find on the moresubstituted carbon of the vicinal halohydrin formed via electrophilic addition to an alkene.
- 18. spatial relationship between the 2 halogens on a ring via electrophilic addition of molecular halogen to an cycloalkene
- 19. the type of reaction hydrogenation is
- 20. type of alkyl halide HBr can give but not HCl and HI.
- 25. the functional group that results from the reaction of a peroxy acid with an alkene