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Unformatted text preview: seconds - NO MORE. 3. How many electrons are involved? 4. Identify the HOMO of the open chain partner. 5. What kind of motion is required as the cyclobutene opens? Why? 6. What product(s) will be formed from a cis-3,4-disubstituted cyclobutene? What product(s) will be formed from the trans counterpart? 7. How will the photochemical reaction differ? The answers are right in the book - Ch. 20, pp 1122-1128....
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This note was uploaded on 03/02/2010 for the course CHEM orgo taught by Professor Jones during the Spring '10 term at NYU.
- Spring '10