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- Following are the steps in the industrial synthesis of glycerin. Provide structures for all intermediate compounds (AD) and describe the type of mechanism by which each is formed.Allylic Bromination: Use of NBS; free radical substitution If it's possible show the mechanismgive reactions and intima mechanism of following reactions-
- (b) acid, HNO3 to produce compound L. The reaction of compound L with bromine, Br2 in the presence of iron tribromide, FeBr3 produced compound M. Benzene also undergoes Fridel-crafts alkylation reaction with chloroethane, CH;CH2CI using catalyst N to produce compound P. Benzene, CeHe undergoes substitution reaction with concentrated nitric Benzena, CsHe menjalani tindak balas penukargantian dengan asid nitrik, HNO, pekat untuk menghasilkan sebatian L. Tindak balas sebatian L dengan bromin, Brz dengan kehadiran ferum tribromida, FeBrs menghasilkan sebatian M. Benzena juga menjalani tindak balas alkilasi Fridel-crafts dengan kloroetana, CH3CH2CI dengan menggunakan pemangkin N untuk menghasilkan sebatian P. (i) Draw the structural formula of L, M and P. Lukiskan formula struktur bagi sebatian L, M dan P. (ii) State catalyst N. Nyatakan pemangkin N. (iii) Show the formation of electrophile that will be reacted with benzene for the formation of compound P.a) Consider the reaction scheme below. -[•] PhLi HONH,, HCI A ELOH B D (i) Deduce the structures of compounds A, D and intermediate C. (ii) Outline the mechanism for the conversion of A to B.please provide the missing organic materials starting materials, reagents/reactions, conditions or organic products in the reaction below. kindly provide and show ther eaction mechanism as well
- Can you explain the rules and the mechanism and provide the resultGive answe of both question just with small explanation Asaap ThanksGive the detailed mechanism for the following nitration reaction. Show the contributing resonance structures and the resonance hybrid for the intermediates. HNO,, H,SO, NO2
- Explain ng distillation process of the combined concentrated hydrochloric acid with 2-methylpropan-2-ol. Explain also the mechanism of their reaction.Q9:- Outline a possible laboratory, synthesis of each of the following compounds from benzene and/or toluene, using any needed aliphatic and inorganic reagents, (a) m-bromophenol (b) 5-bromo-2-methylphenol Q10:- Explain how Esters are more reactive than amides in nucleophilic acyl substitution reactions.divls depends oin the moisture content of the reaction mixture. Propose a detailed mechanism for ench of the following steps to account for the observed The outeome of oxidation of alkenes with 1odine and silver acetate to afford stereochemistry of the product HO () 2, 2 RCO2Ag (i1) NaOH (aq) HO HO () 2, RCO2Ag, H20 (11) NaOH (aq) HO
