What product is formed when each compound undergoes thermal electrocyclic ring opening or ring closure? Label each process as conrotatory or disrotatory and clearly indicate the stereochemistry around tetrahedral stereogenic centers and double bonds. a. b. | Numerade
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Draw the product of each electrocyclic reaction. a. the thermal electrocyclic ring closure of (2E,4Z,6Z)-2,4,6-nonatriene b. the photochemical electrocyclic ring closure of (2E,4Z,6Z)-2,4,6-nonatriene c. the thermal electrocyclic ring opening of cis-5-ethyl-6-methyl-1,3-cyclohexadiene d. the photochemical electrocyclic ring opening of trans-5-ethyl-6-methyl-1,3-cyclohexadiene | Numerade
Draw the product of each electrocyclic reaction. a. the therm…
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