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- 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.Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated , -unsaturated isomers. Propose a mechanism for this isomerization.Which is an alkylation product of benzene? NO2 CH3 NH2 В А A В
- How would you carry out the following syntheses? Cyclohexene Cyclohexanol Cyclohexane ~~시시O -P-O + H₂OName the following organic compound: CH3 S CH CH3 CH 0 CH, CH, 3-methylsulfide-2-ethoxy butane 2-ethoxy-3-methylthio butane O 3-ethoxy-2-methylthio butane O 2-methylsulfide-3-ethoxy butane O 2-ethoxy-3-methylsulfide butane
- What is the product of the following reaction sequence? II CH;CH2CCH; Но* Mg CH;CH2CH2B O 3-methyl-3-hexanol O 2-methyl-3-hexanol 3-ethyl-2-pentanol 2-heptanolChoose reagents to convert 2-cyclohexenone to the following compounds.Which of the following is an acetal? A b с с D d E e c=0 H3C- C CH2 -C-0CH3 Нзс—О— С — ОН A B H3C-OCH2CH2O-CH3 CH-CH3 E