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- supply mechanisms for the following reactions showing all intermediates, all formal charges, and use arrows to show electron flowGive a detailed reaction mechanism for the reaction expected to occur when 2-bromo-2-methylpentane is heated with sodium methoxide. Draw clear structural formulas of all relevant species and use curved arrows to represent electron flow. Also indicate which step is likely to be rate-determining. The answer you sent before will be used for this question.Write complete mechanism for the reactions below use arrows to indicate the direction of electron flow show all intermediates, resonance structures and products
- The electrophilic addition reaction shown below involves a carbocation rearrangement. For the mechanism step below, draw curved arrows to show electron reorganization. Use the arrow tool to specify the origin and the destination of the reorganizing electrons. Consult the arrow-pushing instructions for the convention on regiospecific electrophilic attack on a double bond. I understand how it's supposed to be laid out. I'm just unsure of where the first arrow comes from as there are a lot of positions. I have attached examples on what positions I mean. Thank you.When (1-bromoethyl)cyclopentane is heated in water for an extended period of time, SIX products result: three alcohols and three alkenes. Draw the three alcohols. Draw the three alkenes. Propose a mechanism for the following SN1 reaction. (refer to images) Draw all missing reactants and/or products in the appropriate boxes by placing atoms and connecting them with bonds. Add charges where needed. Electron flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created.Read these directions carefully. For the reaction of 3-methyl-1-propene with Cl2 and H2O shown below, fill in the details of the mechanism. Draw the appropriate chemical structures and use an arrow to show how pairs of electrons are moved to make and break bonds during the reaction. Be sure to write all lone pairs of electrons and all formal charges. Finally, in the boxes provided by the arrows, write which kind of mechanistic element is being indicated, such as "make a bond", "add a proton", etc.
- Give the product and mechanism for the following reaction. Be sure to include all mechanism arrows, lone pairs, and formal charges in your mechanism. The product is an alkene.Complete the mechanism of hydration of alkene below. Please follow curved arrows to predict the resulting structures in each step Step 1 of hydration of 2-methyl-1-propene (Note that the most stable carbocation is formed here) Step 2 of hydration of 2-methyl-1-propene(Note that the most stable carbocation is formed here) Step 3 of hydration of 2-methyl-1-propeneThe following reaction is similar to the dehydration of 2-methylcyclohexanol. However, a significant amount of a terrasubstitued alkene is expected. Predict the structure for this tetrasubstituted alkene. Also, using curved arrows provide a reasonable mechanism for its formation.
- Identify the carbocations that are likely to rearrange, and state whether rearrangement will proceed via 1,2-methyl shift, or a 1,2-hydride shiftPropose a curved-arrow mechanism for this reaction. Use curved arrows to show movement of electron pairs, and draw structures for all important reaction intermediates. Be sure to show all lone pairs and nonzero formal charges.The first step of the addition of a hydrogen halide to an alkene is the addition of H+ to an sp2 carbon to form a carbocation. Predict the carbocation formed in the following reaction and draw the mechanism of its formation. Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron-flow arrows should start on an atom or a bond and should end on an atom, bond, or location where a new bond should be created.