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- Show the stepwise mechanism for the reaction between methanoyl bromide and methyl amine. Use proper arrow formalism to show the movement of electrons in each step.Propose a curved arrow mechanism to account for the formation of compound C.Propose a detailed reaction mechanism for the following conversion
- Arrange the following gem-diols in the order of increasing stability in dilute aqueous acid:Show the electron-flow mechanism of the synthetic schemes (R-Salsolinol) of the picture below. This involves predicting major and by-products using electronic and structural effects. The arrow push mechanism must be shown.(ORGANIC CHEMISTRY) (mechanisms) please give a answer for the following mechanism. Provide a detailed stepwise mechanism for the following transformation.
- Draw the major organic product you would expect to isolate from the reaction of p-bromoethoxybenzene with a misture of HNO3HNO3 and H2SO4H2SO4.Starting exactly with any acid chloride with exactly with 5 carbon atoms, and using appropriate reagents outline the synthesis of the following molecules: (a) 2,6-dimethyl-4-heptanone (b) 4-propyl-4-octanolDraw the detailed reaction mechanism of the vilsmeier hack reaction: preparation of indole-3-carboxaldehyde, using indole, POCl3, DMF, NaOH, and H2O. Include arrows in the mechanism.