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- Outline the synthesis of racemic 3-methyl-3-heptanol, Et(Me)C(*)OHn-Bu, starting from alcohols of four carbons or fewer and any inorganic reagents or solvent needed.4.4 Show how the compound thiodiazine - C21H26N2S2 - decomposes anaerobically and how these end products in turn decompose aerobically to stabilized sulfurand nitrogen compounds.Suppose we aempt the conversion of fumaric acid to deuterated malic acid with BD3·THF,followed by oxidation with D2O2in NaOD(aq). Show all the possible stereoisomers (as Fisherprojections) that may be formed, and draw the mechanistic pathways (showing stereochemistry)that lead to these possible products
- (a) Propose a reasonable synthesis for the formation of nonane from CH3CH2CH2I and any other organic/inorganic reagent. (b) Suggest three (3) different Grignard reactions leading to 2-phenyl-2-butanol.4eplease give the resulting product and explainGive typed explanation 27. Arrange the following molecules in order of increasing acidity CH3CO₂H, H₂O, CH₂=CH₂, CH3CH₂OH
- Draw the resonating structures of aniline and methoxybenzene and discuss whether it is o&p or m-directing and why separatelyGive a clear handwritten answer with explanation..1mry at high temperature , how denturated?(10pts) Compound A, C10H16, was found to be optically active. On catalytic reduction over a palladium catalyst, 2 equivalents of hydrogen were absorbed, yielding compound B, CioH2o. On ozonolysis of A, two fragments were obtained. One fragment was identified as acetic acid (CHCOOH). The other fragment, compound C, was an optically active carboxylic acid, C8H14O2. Write reactions, and draw the correct structures for A-C, explain your answer in detail.
- A chiral amine A having the R conguration undergoes Hofmann elimination to form an alkene B as the major product. B is oxidatively cleaved with ozone, followed by CH3SCH3, to form CH2 = O and CH3CH2CH2CHO. What are the structures of A and B?Explain this result: Acetic acid (CH3COOH), labeled at its OH oxygen with the uncommon 18O isotope (shown in red), was treated with aqueousbase, and then the solution was acidified. Two products having the 18Olabel at different locations were formed.Name the structure. Heating compound A in the presence of H2SO4 results in which product?
