In the presence of aqueous sulfuric acid, (E)-3-methyl-2-pentene can be protonated at two
different carbons to provide two different carbocation intermediates.Draw one energy diagram
showing both possible protonation events.Include in your diagram
a.the product of each of these protonation steps,
b.the relative energies of the transition states leading to these products, and
c.the relative energies of these products.
Correct Answer:
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Q19: Q20: Which of the following statements is true Q21: Use the Hammond postulate to predict which Q22: Draw the product of the following E2 Q23: State the Hammond postulate. Q25: Draw the major organic product of the Q26: Draw a mechanism to rationalize the formation Q27: Draw a mechanism to rationalize the formation Q28: Explain why Reaction A would give more Q29: Which of the following is the product![]()
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