Guided course 05:51Two Steps to Predicting Any Electrocyclic ProductsJohnny Betancourt495views5rank6comments
Multiple ChoiceUse the summary charts to predict the product of the following reactions. If there is more than one isomer possible, draw them 301views2rank2comments
Multiple ChoiceUse the summary charts to predict the product of the following reactions. If there is more than one isomer possible, draw them366views4comments
Textbook Question(•) For the following electrocyclic reactions, did the substituents move in a conrotatory or disrotatory direction? Would you use heat or light to cause movement in this direction? (a)280views
Textbook Questiona. Identify the mode of ring closure for each of the following electrocyclic reactions 1.343views
Textbook Questiona. Identify the mode of ring closure for each of the following electrocyclic reactions 2.309views
Textbook QuestionWhich of the following are correct? Correct any false statements b. A conjugated diene with an antisymmetric HOMO undergoes conrotatory ring closure under thermal conditions.307views
Textbook QuestionWhich of the following are correct? Correct any false statements. a. A conjugated diene with an even number of double bonds undergoes conrotatory ring closure under thermal conditions.326views
Textbook Questiona. Under thermal conditions, will ring closure of (2E,4Z,6Z,8E)-2,4,6,8-decatetraene be conrotatory or disrotatory?b. Will the product have the cis or the trans configuration?230views
Textbook QuestionExplain why compound A will not undergo a ring-opening reaction under thermal conditions, but compound B will.<IMAGE>166views
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