0244Pb18-10.cwk (WP)

0244Pb18-10.cwk (WP) - seconds - NO MORE. 3. How many...

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Problem 18, Chemistry 0244, 2010 To deal with orbital symmetry problems, you MUST have the benchmark cyclobutene-1,3- butadiene opening (and closing) utterly under control. So, even though it is in the book in excessive detail, let s do it here too. You should also take a close look at the “How to do orbital symmetry problems” section in Ch 20 - it starts on p 1165. 1. Draw arrow formalisms for the interconversion of cyclobutene and 1,3-butadiene. 2. Sketch out the pi molecular orbitals for 1,3-butadiene. You should be able to write them in 15
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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.

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