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Please provide a mechanism of synthesis 1,4-diaminobenzene, start from a benzene ring.
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- Select one activator & ortho para director to be on a benzene ring to start. You will then add a bromine to this group showing the COMPLETE mechanism, including all resonance structures. Put a box around the stabilizing resonance structure and explain why it is stabilizing.An appropriate mechanism for the following reaction.What are the reagent to get the product. Please include mechanism
- Propose a synthesis to form cyclohexyl cyclohexanoate using methylene cyclohexane as your only source of carbon. ? oso HINT: There are two cyclohexanes in the product, so this'll definitely involve splitting the starting material in half and doing two paths with it, and joining the two parts at the end...Provide a step synthesis of the following target compoundPlease give product and mechanism for no 2 Alcohol, h2so4