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- complete the following synthesesBy taking into account electronegativity differences, draw the products formed by heterolysis of the carbon–heteroatom bond in each molecule. Classify the organic reactive intermediate as a carbocation or a carbanion.How to synthesize trans-2-methylcyclohexanol from cyclohexanone?
- List the following in increasing order of nucleophilic strength. CH3COO-, H2O, CH3O-, OH-, CH3CH20-Synthesize the products by drawing out reagents and intermediates along the way.4) Draw the complete electron-pushing arrow mechanism for the following reductions. Explain, using resonance contributors, the regiochemistry that results in each case. ỌMe Na, MeOH ? NH3 CHO Na, MeOH ? NH3
- Complete the following reactions by providing the correct product(s), starting materials, or reagents. When appropriate, products should have the correct stereochemistryWhat is the major substitution product for the following reaction? Show the mechanism for the reaction.47) Provide the structure of the major organic product which results in the following reaction. CH₂ Br KI 48) When 1-iodo-1-methylcyclohexane is treated with NaOCH2CH3, the more highly substituted alkene product predominates. When KOC(CH3)3 is used instead, the less highly substituted alkene product predominates. Offer an explanation.