Final Review Game

1234567891011121314151617181920212223242526272829
Across
  1. 2. A unimolecular nucleophilic substitution reaction
  2. 5. The position immediately adjacent to a functional group.
  3. 7. An intermediate containing a positively charged carbon atom.
  4. 13. In a bicyclic system, the carbon atoms where the rings are fused together
  5. 18. A structure corresponding to a local minimum (valley) in an energy diagram
  6. 19. A reaction in which an amino group is treated with excess methyl iodide, thereby converting it into an excellent leaving group, followed by treatment with a strong base to give an E2 reaction that yields an alkene
  7. 20. The study of how energy is distributed under the influence of entropy. For chemists, the thermodynamics of a reaction specifically refers to the study of the relative energy levels of reactants and products
  8. 22. Compounds containing a carbon-carbon triple bond
  9. 23. A compound that does not rotate plane-polarized light.
  10. 25. A compound that can serve as a proton acceptor.
  11. 26. A compound that possesses a hydroxyl group (OH) connected to an sp3-hybridized carbon atom.
  12. 27. A solution containing equal amounts of both enantiomers
  13. 28. A compound capable of functioning as an electron-pair donor.
Down
  1. 1. A conformation in which a hydrogen atom and a leaving group are separated by a dihedral angle of approximately 180°.
  2. 3. In addition reactions, the observation that the hydrogen atom is generally placed at the vinylic position already bearing the larger number of hydrogen atoms.
  3. 4. A reaction that involves the addition of X2 (either Br2 or Cl2) across an alkene
  4. 6. The more substituted product (alkene) of an elimination reaction
  5. 8. An electron-rich molecule or ion that is capable of donating a pair of electrons.
  6. 9. A compound that can serve as a proton donor
  7. 10. A compound that possesses chiral centers and an internal plane of symmetry
  8. 11. A reaction in which the C═C bond of an alkene is cleaved to form two C═O bonds
  9. 12. A reaction in which the configuration of the product is dependent on the configuration of the starting material.
  10. 14. A compound capable of functioning as an electron-pair acceptor.
  11. 15. A lone pair or charge that is participating in resonance
  12. 16. The lowest energy conformation for cyclohexane, in which all bond angles are fairly close to 109.5° and all hydrogen atoms are staggered
  13. 17. A bimolecular nucleophilic substitution reaction.
  14. 21. A carbanion with the structure RMgX
  15. 24. A conformation in which a hydrogen atom and a leaving group are approximately coplanar
  16. 29. An addition reaction in which two groups are installed on opposite sides of a π bond.