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- Reaction of -pinene with borane followed by treatment of the resulting trialkylborane with alkaline hydrogen peroxide gives the following alcohol. Of the four possible cis,trans isomers, one is formed in over 85% yield. (a) Draw structural formulas for the four possible cis,trans isomers of the bicyclic alcohol. (b) Which is the structure of the isomer formed in 85% yield? How do you account for its formation? Create a model to help you make this prediction.Starting with acid chloride with exactly 5 carbon atoms, and using appropriate reagents outline the synthesis of the following molecules:Suggest a synthesis for the molecule below starting from benzene, alcohols of four carbons or fewer and any inorganic reagents for questions D-H please provide the full names for the compounds below
- An unknown hydrocarbon G, whose formula is C16H26 contains two triple bonds. Ozonolysis followed by reduction with (CH3)2S gave CH3(CH2)4CO2H and HO2CCH2CH2CO2H as the only products. Suggest a reasonable structure for compound G.Starting from Benzene explain how compound E could be prepeared. Give reagents, conditions and equations for each step.A nitrile compound is prepared from cyclopentene. The following is an analysis of the disconnection and its synthesis. Write the structure of A and B !
- Provide one alkyl halide of your choice and discuss its structure, nomenclature (systematic and common), physical properties, method/s of preparation, and applications.Describe the ozonolysis of alkenes one mole of a hydrocarbon(A) reacts with one mole of beomine giving a dibromo compound C5H10Br2.Substance A on treatment with cold dilute kMnO4 solution forms a compound C5C12O2(C5H12O2) on ozonolysis A,gives equimolar quantities of propanone and ethanol.Deduce the structure of substance A.Wolff-Kishner reduction of compound W gave compound A. Treatment of A with m-chloroperbenzoic acid gave B which on reduction with LiAH4 gave C. Oxidation of compound C with chromic acid gave D (C9H14O). Suggest the structures for A, B, C, and D.
- Using benzene and any necessary organic or inorganic reagents, suggest efficient syntheses of.Describe and provide a detailed mechanism (use arrow pushing) for the preparation of 2-methyl- 1-butene and 2-methyl-2-buteneSuggest a synthesis for the molecule below starting from benzene, alcohols of four carbons or fewer and any inorganic reagents