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- 10.2 Complete the following reactions: Show the step-by-step process. Do not use shortcut methods. Make it as detailed as it can be. Encode (not hand-written)!What substrate below is ideal for SN1 reaction?Can you pls assist me with the mechanism of Benzyl alcohol being oxidised to Benzyl aldehyde and to Benzoic acid using KMnO4 as an oxidant. Showing arrows and everything.
- Please Write out the mechanism for the multistep synthesis belowEster group (e.g. -CO2Et) is considered a .... Ortho/Para Directing Activator Ortho/Para Directing Deactivator Meta Directing DeactivatorProvide the mechanism for the conversion shown below. CH3Li is effectively H3C-Li+. What type of mechanism is occuring?
- dpredict the product of the following reactions of aldehyde and ketoneComplete the reaction schemes below providing the products of the reaction schemes below.I recovered 3 mL of water, how many grams of water was produced in the reaction please show how? Cyclohexanol can attack the carbocation intermediate formed during the synthesis of cyclohexene. Draw this side product with the molecular formula C12H22O.