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- Draw the constitutional isomer formed when the attached alkenes are treated with each set of reagents: [1] H2O, H2SO4; or [2] BH3 followed by H2O2, −OH.A 2-bromobutane react with methanol and form a enantiomeric pair of 2-methoxybutane. Draw the structures of the enntiomeric pairs of ethers.Which of the isomeric alcohols having the molecular formula C6H14O are chiral? Which are achiral?
- When alkyne A is treated with NaNH2 followed by CH3I, a product havingmolecular formula C6H10O is formed, but it is not compound B. What isthe structure of the product, and why is it formed?Account for the regioselectivity and stereoselectivity observed when 1-methylcyclopentene is treated with reagent. Q) Br2 in H2ODraw the structure of the major product of benzene + CH3CH2CH2Cl in AlCl3
- Draw the structures of the following molecules: (a) trans-l-Bromo-3-methylcyclohexane (b) cis-1, 2-Dimethylcyclobutane (c) trans-1 -tert-Butyl-2-ethylcyclohexaneDraw cyclohex-1-enecarbaldehydea. What alkane, with molecular formula C5H12, forms only one monochlorinated product when it is heated with Cl2? b. What alkane, with molecular formula C7H16, forms seven monochlorinated products (disregarding stereoisomers) when heated with Cl2?
- Draw the organic products formed when cyclopentene is treated withfollowing reagent. (CH3)3COOH, Ti[OCH(CH3)2]4, (−)-DETDraw the products formed when both cis- and trans-but-2-ene are treated with OsO4, followed by hydrolysis with NaHSO3 + H2O. Explain how these reactions illustrate that syn dihydroxylation is stereospecic.Draw the constitutional isomer formed when the following alkenes are treated with each set of reagents: [1] H2O, H2SO4; or [2] BH3 followed by H2O2, −OH.