For the following reaction: 2) Draw both the organic and inorganic intermediate species. Include nonbonding electrons and charges, where applicable. 1) Add curved arrows for the first step. СHз Н H Нзс н н :ci: Нас- -CHз H н
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- For the reaction can someone please synthesize the given products from the given reactants. Multiple reactions/steps will be needed (the arrows designate the minimum number of steps). Also, for the 1st step (reaction) in each synthesis, can you please draw an energy diagram showing the correct number of hills and valleys for that step’s mechanism?Draw a curved arrow mechanism for the reaction. You can assume that all reactants and products are shown. Add/Remove step CN :C=N:ORGANIC CHEMISTRY: Is this mechanism for dibenzalacetone formation complete? arrows and electrons, and formal charges?. If no, please provide the complete mechanism. From this mechanism in the picture, identify the intermediate benzalacetone.
- Consider the reaction. CH3 H :Ci: C=C H-Ci: H3C- -CH3 H3C CH3 H. Add curved arrows for the first step. Draw both the organic and inorganic intermediate species. Include nonbonding electrons and charges, where applicable. Include hydrogen atoms. H CH, H CI - ci H,C CH, C. H H -C H H H H MacBook AirPlease do not draw the same proudct more than once in a reactiona) Consider the reaction of HBr with ethylene and propylene. At roomtemperature the reaction of propylene with HBr is much faster than thereaction with ethylene.Using reaction energy diagrams and your knowledge of carbocationstability explain why this is so. b) Xylene (dimethylbenzene) is a commonly used chemical in the printingindustry and as a cleaning solvent for oily waste. It is also used whenpreparing histological samples to remove waxes from biological samples.Draw the three possible structures for this compound and give the UPACnames for each. Define which structures are ortho, meta, and para.
- Where do the arrows for this are suppose to go? (Intermediate) Reactant Mechanism Explorer: Sketch and Submission (Intermediate) Reactant Tip: Only add curved arrows in this sketcher Mechanism Explorer: Sketch and Submission (Intermediate) Reactant CH H H₂O Tip: Only add curved arrows in this sketcher leshow complete reaction mechanism, with steps, and arrowsIn Part 1 add the curved arrows to the nucleophilic acyl substitution reaction mechanism. In Part 2, answer the multiple-choice question about the reaction in Part 1. Part 1 See Periodic Table O See Hint :ö: :Br: Add the missing curved arrow notation. 20 F CI Br I Part 2 Which statement is most correct regarding the equilibrium for the above reaction? Choose one: O The equilibrium favors the right (i.e., Kea > 1) because acetate is a better leaving group than bromide. O The equilibrium favors the right (i.e., Keg > 1) because bromide is a better leaving group than acetate. O The equilibrium favors the left (i.e. Keg « 1) because acetate is a better leaving group than bromide. O The equilibrium favors the left (i.e., Keg« 1) because bromide is a better leaving group than acetate.