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- Study the curved arrows in the reactions below and provide the structures of theproduct(s) formed. One block may represent more than one product/by-product.A certain hydrocarbon, C7H10, yields the two products shown below upon oxidative cleavage with KMnO4/H3O+ . Deduce the structure of the hydrocarbon.When pyrrole is added to a dilute solution of D2SO4 in D2O, 2-deuteriopyrrole is formed. Propose a mecha-nism to account for the formation of this compound.
- Please write out the mechanism for the acid (WHICH IS 3-BROMOBENZOIC ACID) reacting with anilide. PROVIDE THE MECHANISM AND BRIEFLY EXPLAIN THE STEPS OCCURING PLEASE1)2PbS + 3O2 on heating gives 2PbO + 2SO2 2)PbS + 2O2 on heating gives PbSO4 Why is it that 2 reaction shows different products? Please explain in detailI need help to find the mechansim for Preparation of Cyclohexanone by Hypochlorite Oxidation and explain the mechanism in detail
- When N-bromosuccinimide is added to hex-1-ene in CCl4 and a sunlamp is shone on themixture, three products result.(a) Give the structures of these three productsI need help to find the mechansim for Preparation of Cyclohexanone by Hypochlorite Oxidation and explain the mechanisms step by step so I can understand it pleaseWhen 3-methyl-1-butene is reacted with 9-borabicyclo[3.3.1]nonane, the "1-ol" product is formed. What is the detailed reactin scheme for the transformation? Describe the purification procedure.
- Protein: SHAYNERSE Predict the products of the following reactions with the protein given, if there is none, write NO RXN. Hg/HNO3 HNO3I need help to find the mechansim for Preparation of Cyclohexanone by Na2CrO3/H2SO4 and explain the mechanisms step by step so I can understand it pleaseSuggest an explanation for the fact that the order of reactivity of the halides toward n-butylbrosylate in acetone is Cl” > Br” > I~ when (C4H9)4N* is the cation of the halide salt butI” > Br” > Cl” when Li’ is the cation