Across
- 5. Formation of the less substituted alkene
- 8. A type of nucleophilic substitution where the nucleophile is a solvent molecule
- 12. When the reaction chooses one product over the other
- 13. The more substituted halide is formed from the addition of H-X to an alkene
- 15. Replacement of one group by another
- 16. Where carbocations with filled C-H bonds overlap with empty 2p orbitals
- 17. Step where two radicals combine
- 18. Branch of chemistry which deals with the spatial arrangement of atoms and groups in molecules
- 20. The radical forming step
- 22. A type of elimination where the most substituted alkene predominates due to hyperconjugation stabilising the transition state
Down
- 1. The preferential formation of one isomer over the other
- 2. Front side approach, the tetrahedral umbrella would be retained
- 3. Disubstituted on adjacent (1,2) positions
- 4. When more than one orientation is possible in the product
- 6. Donates a pair of electrons
- 7. When two substituents are removed from a molecule during a mechanism
- 9. Radical reaction and radical regenerations
- 10. Nucleophile approaches from the rear of the departing atom, the tetrahedral umbrella is inverted
- 11. Consists of a single molecule
- 12. A mixture that contains both enantiomers of a compound which are present in equal amounts
- 14. Addition of a proton to a molecule
- 19. The slowest step of a chemical reaction that determines the speed the overall reaction proceeds at
- 21. Step by step sequence of reactions