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- Part a) Draw step by step arrow pushing mechanism for formation of X. Please make it neat and detailed. Part b) Draw Y.Draw another reasonable resonance structure for the intermediate product given the other two. draw structure ... --------- 80 CH-CH₂CH₂ →Type in the correct IUPAC name and spelling of the following compounds. Please note proper notations (like hypen and commas) to avoid invalidating your answers.
- a) Write out the 3-step arrow pushing mechanism showing how 1-pentene is hydrated to make 2-pentanol. b) Draw the other 2 alkenes(don’t forget cis/trans isomers!) that could also be hydrated to make 2-pentanol. Briefly explain why1-pentene is the best choice.G.304.Part a) Draw step by step arrow pushing mechanism for formation of X. Please make it neat and detailed. Part b) Draw Y. NABH4 МеОн ОН LAH THE
- Draw the principal organic product for the reaction of 2-bromopropane with magnesium in diethyl ether, followed with 2-butanone in diethyl ether, and then followed by dilute acid. Click and drag to start drawing a structure. 0PLEASE SHOW STEP BY STEP, WITH ARROWS! ALSO PLEASE INCLUDE ALL ELECTRON LONE PAIRS AND CHARGES FOR STRUCTURES IF NECESSARY!Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. H ..:OH: Select to Add Arrows HCI H H H H H :CI: OH, Најан Select to Add Arrows !
- Give a systematic or common name for attached compoundA certain hydrocarbon had the molecular formula C16H26 and contained two triple bonds. Ozonolysis gave CH3(CH2), CO₂H and HO₂CCH2CH2CH2CH2CO₂H as the only products. Draw a reasonable structure for this hydrocarbon. Click and drag to start drawing a structure. D:Please don't provide handwritten solution..... what is the product for this substitution reaction below