Draw all four products that are expected when 2-ethyl-3-methyl-1,3-cyclohexadiene is treated with one equivalent of HBr
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Draw all four products that are expected when 2-ethyl-3-methyl-1,3-cyclohexadiene is treated with one equivalent of HBr
* Incorrect. Identify the location where protonation can occur. Which of the four mechanistic steps is shown in this step of the mechanism? Draw step 1 of the mechanism for the protonation at C4 position. CH₂ -CH₂ * Incorrect. Please delocalize the charge accordingly. CH₂ Edit Drawing Draw the resonance structures for the cation intermediate formed in the previous step. CH₂ Edit Drawing CH₂ CH, CH₂
* Incorrect. Identify the location where protonation can occur. Which of the four mechanistic steps is shown in this step of the mechanism? Draw step 1 of the mechanism for the protonation at C1 position. "CH₂ "CH₂ Edit Drawing * Incorrect. Please delocalize the charge accordingly. CH₂ Draw the resonance structures of the cation intermediate formed in the previous step. Edit Drawing CH₂ "CH₂ CH, CH₂