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Explain why 1,4-pentadiene is less acidic when compared to cyclopentadiene
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- which is an untrue statement concerning the diels alder reaction? A) the reaction is an anti addition B) the reaction occurs in a single stepWhat do you mean by Cumulated dienes ?How would you develop a molecular orbital for a structure like buta-2-diene that has an anion on the first carbon and a cation on the fourth carbon? Also, how would MO look like for 2-dimethyl-1,3-pentadiene?