1) Propose a plan to synthesize 2,2,3-Trimethylpentan-3-ol: 2) Predict & draw the products of the ff alcohols in reaction with PCC: CH3 HC- CH 애 OH 3) Propose a plan for the synthesis of 3-Phenylpentan-3-ol:
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Questions 1 and 3 only and please provide the structural formula in the plan (do not shorcut pls) and pls explain thank you
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- Draw and upload a reaction scheme to show how you would make butan-2-one starting from but-1-ene clearly showing products and needed reagents.Hint: multiple reactions are required!Please help with F-M, the questions Complete the following reactions which form ethers (A and B) and cyclic ethers (C-E) as major productsOxidation of cholesterol converts the alcohol to a ketone. Under acidic or basic oxidationconditions, the C“C double bond migrates to the more stable, conjugated position. BeforeIR and NMR spectroscopy, chemists watched the UV spectrum of the reaction mixture tofollow the oxidation. Describe how the UV spectrum of the conjugated product, cholest-4-en-3-one, differs from that of cholesterol
- Starting with cyclohexanone, show how to prepare these compounds. In addition to the given starting material, use any other organic or inorganic reagents as necessary. Q.) CyclohexeneGive the structure of the principal product(s) when each of the following alcohols reactswith (1) Na2Cr2O7>H2SO4, (2) PCC, (3) DMP, and (4) 1 equiv NaOCl-TEMPO.(a) octan-1-ol (b) octan-3-ol(c) 4-hydroxydecanal (d) 1-methylcyclohexan-1,4-diolLike alcohols, ethers undergo a cleavage by breaking a carbon–carbon bond between an alkyl group and the carbon bonded to the ether oxygen atom; that is, the red C–C bond in R–CH2OR' is broken. With this in mind, propose structures for the fragments formed by a cleavage of (CH3)2CHCH2OCH2CH3. Suggest a reason why an ether fragments by acleavage.
- The alcohol compound güven the formula below is used in perfume making.bromine benzeme and -1 synthesis of this compound using the necessary organic and inor chemicals showWhich of the choices below will not provide an ether as a product?a. reacting an alcohol with an alkyl halideb. reacting an alkene with mCPBAc. reduction of alcohold. reacting alcohol with a strong aciddedcue the major organic product from the following reations. be ablw to draw hydration halogenation hydrohalogenation, halohydrin formation, oxymercuratiom demercuration qnd hydroboration oxidation.
- Oximene and myrcene, two hydrocarbons isolated from alfalfa that have the molecular formula C10H16, both yield 2,6- dimethyloctane when treated with H2 and a Pd catalyst. Ozonolysis of oximene forms (CH3)2C = O, CH2 = O, CH2(CHO)2, and CH3COCHO. Ozonolysis of myrcene yields (CH3)2C = O, CH2 = O, (two equiv), and HCOCH2CH2COCHO. Identify the structures of oximene and myrcene.The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?As a rule, axial alcohols oxidize somewhat faster than equatorial alcohols. Which would you expect to oxidize faster, cis-4-tert-butylcyclo-hexanol or trans-4-tert-butylcyclohexanol? Draw the more stable chair conformation of each molecule.