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Unformatted text preview: Each correct name is worth 3 points. 3. 2-Methyl-4-methylene-2-hexene 4. 1,6-Dimethyl-1,5-cyclohexadiene 2-Ethyl-4-methyl-1,3-pentadiene 2,3-Dimethyl-1,3-cyclohexadiene 2 5. (4 points) When methylenecyclopentane is exposed to HCl, a single, achiral product is formed. Please draw the structure of this product in the empty box below. 6. (12 points) In the space below, propose a mechanism for the reaction described above. Use curved arrows to show movement of electron pairs, and be sure to draw structures for all important reaction intermediates. If an intermediate is a resonance hybrid, please draw all important contributing resonance structures. For full credit, your mechanism needs to be consistent with the product you drew in your answer for Question 5! HCl Cl CH 3 H Cl H Cl Cl CH 3...
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- Spring '09
- Organic chemistry, line-angle structure, Cl Cl CH