Organic Chemistry
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Provide a plausible mechanism for the following reaction.
Illustrate the results of the given sigmatropic rearrangements reactions:
Classify the given sigmatropic rearrangement reaction.
Describe the electron rearrangement which happens in each reaction with arrows.
A deuterated compound was used in the given reaction. Explain why it is utilized.
Determine the product of the reaction given below.
Demonstrate the arrow pushing in the rearrangement of 2-iodo-5-methylcyclopenta-1,3-diene to yield 1-iodo-4-methylcyclopenta-1,3-diene and 5-iodo-2-methylcyclopenta-1,3-diene.