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- Show the process of synthesizing 2-methyl2-cyclohexenone from 2-methyl cyclohexanone. Write down the stages of the monocyclic reaction process in detail.Provide the mechanism for the conversion shown below. CH3Li is effectively H3C-Li+. What type of mechanism is occuring?The synthesis above can be performed with some combination of the reagents listed below. Give the necessary reagents in the correct order. Be sure to consider stereochemistry and regiochemistry.A. NaOHB. mCPBAC. OsO4, tBuOOHD. NaHE. H2, LindlarF. CH3CH2CH2BrG. CH3CH2ClH. NaNH2I. H3O+J. Na, NH3(l)
- Propose a mechanism for the following cycloaddition reactionDraw mechanism arrows and then predict the major products and stereochemistry. Also include the labels of thermodynamic and kinetic 3,4-dimethylhex-3-ene with HClPlease show the reaction mechanisms of the [3 + 2] cycloadditions of (A) Ozone and (B) OsO4 to cis-2-butene to form their respective 5-membered rings.
- Show the mechanism and give the products for the following reaction. Pay attention to regio/stereo-chemistry.Draw mechanism arrows and then predict the major products and stereochemistry. Also include the labels of thermodynamic and kinetic 1-methylcyclohexene with BH3 followed later with –OH, H2O2, and H2O.In the presence of acid such as H2SO4, 3,4-dimethyl-1-pentene undergoes isomerization to 2,3-dimethyl-2-pentene (shown below). Write a complete mechanism, showing all steps and using curved arrows to explain this observation.
- Ochem help... Please provide the structures for the products obtained in the reaction schemes below (see image)provide the product reaction shown below. Include stereochemistryWrite down all possible alkene products from the following Elemination reaction (no mechanism is required) indicate which one will be major product. And explain it?