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- 1) Me2NH, CH3CO2H 2) 3) H3O* please provide mechanism with stepsDraw a plausible mechanism for the reaction shown below. Et Ме OH ..Me 1) Excess EtMgBr 2) Hо Et "CI3. Provide the mechanism for the following reversible nucleophilic addition. Show all curved arrows and intermediates. cat. H+ H₂O HO OH H H 1) protonate to activate 2) nucl adds 3) deprotonate what stays
- A H2N. Figure 9: Multi-step reaction sequence↑ ... Propose a reasonable stepwise mechanism, using curved arrow notation to show the flow of electrons, for the following reaction. KCN H EtOH, H₂O OH 02N O₂N NO2 Tt O ọ ♡ > ՐH₂C H H₁C Br NBS CH, CH₂ CC, hv **You may assume that Br-Br is formed by a side reaction that occurs (which we discussed in class). This is useful for one of the steps of the mechanism.