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- (Give cleat handwritten solution) Give missing reagent in the given reaction for all subparts!Propose a reasonable stepwise mechanism, using curved arrow notation to show the flow of electrons, for the following reaction. O₂N H KCN EtOH, H₂O O₂N OH NO₂Question: Draw the mechanism of the reaction you will complete in lab. Use the proper arrow drawingconvention to show all bond making and bond breaking steps in the reaction. Background info: A substitution reaction takes place when a nucleophile (Nu:) forms a bond with a carbonatom, displacing a leaving group (L).SN2 reactionLeaving groups are typically weak Bronsted bases that are stable as anions (often halide anions).The precise timing of when the leaving group leaves depends on the structure of the substrate –the molecule bearing the leaving group. Methyl and primary alkyl halides tend to undergo SN2type reactions. In this type of reaction, the nucleophile attacks the carbon from the side oppositethe leaving group and the nucleophile-carbon bond is made simultaneous with the carbon-leavinggroup bond breaking. SN2 reactions are one-step and there is an inversion of stereochemistry atthe carbon bonded to the nucleophile.SN1 reactionIf the carbon undergoing substitution is…
- A. B. C. D. E. Br Br H H OH Which of these synthetic6. Explain why halogenation occurs twice in the following reaction. Ch₂ NaOH give both answer asap thanks 7. Draw a complete, detailed mechanism for the following reaction. Label the electron-rich and electron-poor sites in each step. H₂SO₂ OSOHSynthesis - Drawing Saved Synthesize the following compound from cyclohexanol, ethanol, and any other needed reagents. он Part 1 out of 2 plnts Preparation of organometallic reagent: еВook Print References A B CH3CH2OH CH3 CH2MGB. draw structure ... Draw the intermediate product above and select the correct reagent for A. O Br, O NaBr O HBr O Select the correct reagent for B. O Mg O MgBr2 O MgI, O MgO Hin Soluti raw 11 e here to search
- Mechanism. Provide the complete mechanism for the reaction below. You must include appropriate arrows, intermediates, and formal charges. OH HO, H2SO4 (cat.) reflux3) Draw the major organic product generated in the reaction below. CH3 HCI |Draw the major organic product generated in the reaction below. Pay particular attention to regio- and stereochemical detail.
- A student attempted to synthesize an epoxide according to the reaction scheme shown here, but no epoxide was formed. Explain why. Hint: It may be helpful to build a OH NaOH No epoxide model of the reactant molecule. (H3C);C' Br3) Explain how and why the reaction below results in the observed regiochemistryand/or stereochemistry.Copy the given reaction and show the mechanism by supplying the appropriate curved arrows. Also, identify the general type of reaction mechanism (polar or non-polar). For polar reaction mechanisms, label the nucleophile and the electrophile. :0: :0 O.. H. HÖ: Hö: