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for my final example I will use a reaction that has recently appeared on the exam of one of my or ghost students for the starting material I have a cyclo butane with an alkene coming off the rink for my final product I have a substituted cyclopentanone so how did I go from a cyclo butane to a cyclopentane and unfortunately this type of question always catches students looking at it at first glance I may not know the answer but if I tackle this mechanism one step at a time based on concepts that I know I trust that I will come up with the right answer there are two things I want to recognize before starting this reaction the first is that anytime you are given water reacting in an acid catalyst this means that were using h3o plus in the reaction or simply H+ whichever you feel more comfortable with the second thing I want to recognize is the ring strain and thus the instability of the cyclobutane while the carbons in the ring are sp3 and that means they prefer to have a bond angle of