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Treatment of α,β-unsaturated carbonyl compound X with base forms the diastereomer Y. Write a stepwise mechanism for this reaction. Explain why one stereogenic center changes configuration but the other does not.
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- To my understanding that you are supposed to answer 3 questions per asking . Write clear and mine form as questions thank youpart, g,h,iOn a balance mass an amount of potassium hydrogen phthalate (KHP) needed to neutralize approximately 12 ml of 0.1 M NaOH(aq), and completely transfer the KHP to a clean 125-ml Erlenmeyer flask. Record the mass of the KHP at least to The thousandth decimal place. please answere
