Chapter 27: Q 24. (page 1096)
Question: What product is formed from the Claisen rearrangement of each starting material?
Short Answer
Answer
a.
b.
c.
Chapter 27: Q 24. (page 1096)
Question: What product is formed from the Claisen rearrangement of each starting material?
Answer
a.
b.
c.
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Get started for freeQuestion: A solution of 5-methylcyclopenta-1,3-diene rearranges at room temperature to a mixture containing 1-methyl-, 2-methyl-, and 5-methylcyclopenta-1,3-diene. (a) Show how both isomeric products are formed from the starting material by a sigmatropic rearrangement involving a CโH bond. (b) Explain why 2-methylcyclopenta-1,3-diene is not formed directly from 5-methylcyclopenta-1,3-diene by a [1,3] rearrangement.
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.
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