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- What reaction took place in the reaction below? CHẠCH, CH; CH,(CH),CH; CH{CH,),C-OCH; CHẠCH)A CH; CHỊCHCo H0 НОСН CH/CH),CH, CH, (CH),C-C HOCH, HH O reduction (hydrogenation) O amide synthesis O acetal hydrolysis O ester synthesis O acid base O dehydration O thioester synthesis O phosphate ester synthesis O hydration O ester hydrolysis O amide hydrolysis O oxidation O acetal synthesisComplete the following reactions (draw the correct final products)?Predict the major product for the reaction. H Cl₂, CH3CH₂OH
- 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?Complete the reactions by drawing the structure of the reactants or product(s) & O a) HO. OCH3 + O c) b) H3CO. CH3OH d) HO- OCH3 OH H+Give the major product AND name for the reaction.
- What products result from each step in the following reactions? Use mild acid if needed. q H₂O, H+ TfCl MeOH + + + TfCl MeOHo Predict the two major organic products of the reaction. (HI behaves as an HX reagent.) H₂C ΤΟ + CH3 H—I CH3 Draw the two major organic products. H₂C H H CH₂ CH₂Draw the major product of this reaction. Ignore inorganic byproducts. HCI, H₂O Drawing <