Why is the compound/isomer on the right easier to make? it is definetly the right one, and both go through conrotatory rotation, but im confused on what the two would look like after the rotation, i think its looking at what the 2 isomers look like after conrotaotry rotation i can see sterics better and decide on an answer, but im confused on how to do that with such a complex molecule
5. The following cyclobutenes can be opened to butadienes under thermal conditions. They react at very different rates. Which reaction is fast and which one is slow? Provide your reasoning. Hint: The ring opening of the cylcobutenes occurs with the same conrotatory or disrotatory movement as the ring closure from butadienes. H H H H
