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- 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 first step of this reaction sequence. Be sure to account for all bond-breaking and bond- making steps. I H BH₂ H B H Select to Add Arrows > H Bll H BH₂Curved 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 steps. Be sure to account for all bond-breaking and bond-making steps. H H y H H ✪ I CH3OH heat CH3OH heat HH H : Br: O CH3OH heat Drawing ArrowsCO2 Follow the curved arrows and draw the product of this reaction. You do not have to consider stereochemistry.
- Question 5 1). Draw all resonance structures for the carbocation intermediate formed by para attack; circle the resonance structure that is particularly unstable. N- N Cl₂ AICI 3 H 2). Draw all resonance structures for the carbocation intermediate formed by ortho attack; circle the extra resonance structure that is particularly stable. H a Aer ANSAS C HNO3 H₂SO4Add any remaining curved arrows to show the two propagation steps that form the observed products. Do NOT add curved arrows to convert the first resonance structure into the second resonance structure. 3r- ErDraw the mechanism and the energy diagram for the reaction shown below. Include any resonance structures for the intermediates of the reaction. H3O+
- ow the mechanism for the following reaction conducted at -5 °C in CC14: cyclohexene + bromine yields a dibromocyclohexane Draw structures - including charges and electrons - and add curved arrows. Details count. Step 1 Add three curved arrows to the first step. Draw the step 1 products: 1 organic species; 1 inorganic species. Step 2 • Reproduce the step 1 products. Add two curved arrows to show the bromide ion reacting with the organic species. Draw the final product. 1L o ↑ MapDraw the product of syn addition of H2 across the double bond of the alkene in the drawing area below.If reacted with Cl2 how many distinct mini chlorinated products will be present? How many monocholtinated products will form at 1 and 2? Which Carbon will be attached to a Cl in the major product?