The mechanism of conversion of benzene to allyl-4-chlorobenzene is as shown below:
Give stepwise mechanism for the reaction. show
intermediates and electron movement.
c. Cl CH₂ - CH = CH - O- CH₂ H H + eltz OH + HCl.
Provide a full mechanism for the following reaction. Include
intermediates, formal charges, and curved arrows to show electron
flow.
Provide a full mechanism for the following reaction. Include intermediates, formal charges, and curved arrows to show electron flow. H20, H о нон, он вме OH HN
please draw the full mechanism with all electron pushing arrows, reactant structures, intermediates, and products for the hydroboration oxidation reaction using 1-octene to prepare 1-octanol.
Please write the mechanism for the acid catalyzed hydrolysis
of this compound. Show intermediates, formal charges, and lone
pairs. Use curvy arrows.
0
Provide a mechanism for the following reaction. Please show all intermediates and use arrows to show the movement of electrons. Propose a synthesis for the following compound. You may use any reagents needed. Complete the synthesis in 4 steps or less (more than one step is needed).
3) The starting materials, two intermediates, and the product of the three-step mechanism are show below. Add the curved electron arrows to explain the mechanism below Draw the energy diagram for the reaction to the right. This wl include the two intermediates and three transitions states of the correct relative energies. Consider the rate determining step and the stability of the intermediates to draw it accurately Itermediate stability follows the same rules E as good Lewis structures - more stable...
please show/explain the mechanism and products of the reaction:
Cl t-BuO
explain the mechanism in words
c Draw the full electron-pushing mechanism (using proper electron-pushing arrows, intermediates, and structures) for the synthesis of phenolphthalein from phenol and phthalic anhydride. It's an electrophilic aromatic substitution reaction!
c Draw the full electron-pushing mechanism (using proper electron-pushing arrows, intermediates, and structures) for the synthesis of phenolphthalein from phenol and phthalic anhydride. It's an electrophilic aromatic substitution reaction!
please answer and show work.
8. The mechanism for the formation of highly reactive Criegee intermediates in the atmosphere is shown below (the biradical product is the Criegee intermediate): ko The third step is the slowest. What is the predicted RATE LAW for this reaction?
Propose a mechanism consistent with the following reactions (you must show all the intermediates and electron flow to receive full credit) (3 x 3-9 pts) 6. HF 9