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- at product will result from the reaction shown? (Just mention the class of compound not the nomenclature) CH3 HOCH,CH,OH CH;CHCH,CH,CH,C-H H+To preview image Click Here! a. Give the curved arrow-pushing and the Allowed product of the following cycloaddition. State whether the product is achiral, a meso compound, a pure enantiomer or a racemic mixture. H&CO OHC A B CHO heat b. Draw the HOMO for reactant A and the LUMO for reactant B on top of the structures below H₂CO 3 A HOMO OHC B LUMO CHO c. Does the allowed reaction proceed suprafacial/suprafacial or suprafacial/ antarafacial↑ ... 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 ♡ > Ր
- 1. Draw the mechanism for the following reaction. Include all intermediates, formal charges, and arrows. ol CH3CH₂NH2 H*, -H₂ODraw the complete, detailed mechanism (curved arrows) for the following reaction. Br 2. H₂O OKDraw the products of the reaction shown. Electron flow is indicated with curved arrows. H₂C CI:
- Mechanism of this reaction please!Draw the final product of this series of reactions. |||** OH 1. SOCI₂ 2. NaCN • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If more than one product is possible, only draw the major product. • If the reaction produces a racemic mixture, draw both stereoisomers.For the following reaction: Explain how to decide which mechanism(s) the reaction will follow including information about: o alkyl halide substitution (what type and what this tells you about the preferred mechanism) o nucleophile or base strength o solvent (what type and how this affects the mechanism) State which mechanism(s) will occur.". Draw the mechanism. Draw the product(s). *
- What reagents, and or solvents/temperature belong below and above the arrow to produce the final product on the right2) Use your understanding of reaction rates to identify the faster reaction for each of the following pairings. HC Br O CECH Br 2 equiv of OR H NH2 Br 2 equiv of ONH2 BrDraw the most stable resonance form for the intermediate in the following electrophilic substitution reaction. _NH2 NH2 Br2 Br • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.
