Chapter 27: Q 50. (page 1103)
Question: What type of pericyclic reaction is illustrated in each reaction?
Short Answer
Answer
Chapter 27: Q 50. (page 1103)
Question: What type of pericyclic reaction is illustrated in each reaction?
Answer
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Get started for freeQuestion:What product would be formed by the disrotatory cyclization of the given triene? Would this reaction occur under photochemical or thermal conditions?
Question: Draw the product formed when diene M undergoes disrotatory cyclization. Indicate the stereochemistry at new hybridized carbons. Will the reaction occur under thermal or photochemical conditions?
Question:Using the WoodwardโHoffmann rules, predict the stereochemical pathway for each cycloaddition:
(a) a [6 + 4] photochemical reaction;
(b) an [8 + 2] thermal reaction.
Question: When both carbons ortho to the aryl oxygen are not bonded to hydrogen, an allyl aryl ether rearranges to a para-substituted phenol. Draw a stepwise mechanism for the following reaction, which contains two [3,3] sigmatropic rearrangements.
Question: For each molecular orbital in Figure 27.2, count the number of bonding interactions (interactions between adjacent orbitals of similar phase) and the number of nodes. (a) How do these two values compare for a bonding molecular orbital? (b) How do these two values compare for an antibonding molecular orbital?
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