Chapter 30: Q25 E (page 1033)
Which of the following reactions is more likely to occur? Explain.

Short Answer
To identify which among the two reactions is more likely to occur can be stated.
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Chapter 30: Q25 E (page 1033)
Which of the following reactions is more likely to occur? Explain.

To identify which among the two reactions is more likely to occur can be stated.
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Vinyl-substituted cyclopropanes undergo thermal rearrangement to yield cyclopentenes. Propose a mechanism for the reaction, and identify the pericyclic process involved.
What stereochemistry would you expect for the product of the Diels–Alder reaction between (2E,4E)-2,4-hexadiene and ethylene? What stereochemistry would you expect if (2E,4Z)-2,4-hexadiene were used instead?
Ring-opening of the trans-cyclobutene isomer shown takes place at much lower temperature than a similar ring-opening of the cis-cyclobutene isomer. Explain the temperature effect, and identify the stereochemistry of each reaction as either conrotatory or disrotatory.
Do the following electrocyclic reactions take place in a conrotatory or
disrotatory manner? Under what conditions, thermal or photochemical, would you carry out each reaction?

Photolysis of the cis-cyclobutene isomer in Problem 30-35 yields cis-cyclododecaen-7-yne, but photolysis of the trans isomer yields trans-cyclododecaen-7-yne. Explain these results, and identify the type and stereochemistry of the pericyclic reaction.
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