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- i) H ii) H-C 6. Starting from the alkyne shown below, show all reagents and intermediates necessary to carry out the following conversions to the products shown. You can use any alkyl halide. More than one step is required. H C-H OH OH HGive the major product(s) of the following reaction. H2O, H+ H heatPlease include the names for products A and B, thanks!
- H₂SO4, H₂O Choose the enol(s) that can be formed from the following oxymercration reaction. OH ОН OH HgSO4 ОНComplete the following reaction. H₂ A OH B FU O=O CH3 OH HO KMnO4 H₂O, heat C H₂ CH3 D OH CH H₂ CH3When (CH3CH2)3CBr is added to CH3OH at room temperature, the major product is (CH3O)C(CH2CH3)3 and a minor product is CH3CH=C(CH2CH3)2. Propose a mechanism for the product that is formed by the substitution reaction. Use curved arrows to show the movement of electrons.
- What is the major organic product obtained from the following reaction? H₂Cr₂O7 H₂SO4, H₂O OH A) 1-butene, CH3CH2CH-CH₂ B) butanal, CH3CH₂CH₂CHO C) butanone, CH3CH₂COCH3 D) butanoic acid, CH3CH2₂CH₂COOHGive the major product for the reaction5. Describe an efficient synthesis of 1-methyl-1-cyclohexanol from cyclohexanol. Show the structure of the reagents, reactants and products from each step. Cyclohexanol -------> -----> 1-methyl-1-cyclohexanol