Chapter 27: Q 1. (page 1078)
Question: Classify each reaction as an electrocyclic reaction, a cycloaddition, or a sigmatropic rearrangement. Label the σ bonds that are broken or formed in each reaction.

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Chapter 27: Q 1. (page 1078)
Question: Classify each reaction as an electrocyclic reaction, a cycloaddition, or a sigmatropic rearrangement. Label the σ bonds that are broken or formed in each reaction.

Answer




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Question: What type of cycloaddition occurs in Reaction [1]? Draw the product of a similar process in Reaction [2]. Would you predict that these reactions occur under thermal or photochemical conditions?

Question: What product is formed when each compound undergoes a photochemical electrocyclic reaction? Label each process as conrotatory or disrotatory and clearly indicate the stereochemistry around tetrahedral stereogenic centers and double bonds.

Question: a) What product is formed when triene N undergoes thermal electrocyclic ring closure? (b) What product is formed when triene N undergoes photochemical ring closure? (c) Label each process as conrotatory or disrotatory.

Question: Using the Woodward–Hoffmann rules in Table 27.4, predict the stereochemistry of each reaction.
a. a [6 + 4] thermal cycloaddition
b. photochemical electrocyclic ring closure of deca-1,3,5,7,9-pentaene
c. a [4 + 4] photochemical cycloaddition
d. a thermal [5,5] sigmatropic rearrangement
Question:What product would be formed by the disrotatory cyclization of the given triene? Would this reaction occur under photochemical or thermal conditions?

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