1.) Consider the reaction of 2-methyl-1,3-cyclohexadiene with
HCl. Assuming that the reaction takes place at a very low
temperature: (a) draw the intermediate and product structures,
including any formal charges. Please answer all parts a, b, and c. 2.) For each addition route of the reaction, draw the
structure(s) of the major product(s), including
stereochemistry. There are two products for each addition reaction. Consider the reaction of 2-methyl-1,3-cyclohexadiene with HCI. Assuming that the reaction takes place at” a very low temperature: draw the intermediate and product structures, including any formal charges. What is the major product of the reaction at very low temperatures? Is the reaction under rate control or equilibrium control under the conditions stated above?
1) 2-methyl-1,3-cyclohexadine reacts with HCl at a very low temperature. At this temperature, a 1,2 addition product is the major product HCI More stable resonance formLess stable resonance form CI CI CI CI 1,2 addition product 1,4 addition product b) The major product of the reaction at very low temperatures is the 1,2 addition product c) At low temperature the reaction is under rate control (kinetic).
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