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What is the major product? Please explain
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- Define the following terms: a. reaction mechanism b. carbocation c. enediol d. general acid e. general baseProvide the product(s) for the following reaction. If no reaction, draw the starting materials.I recovered 3 mL of water, how many grams of water was produced in the reaction please show how? Cyclohexanol can attack the carbocation intermediate formed during the synthesis of cyclohexene. Draw this side product with the molecular formula C12H22O.
- A hydrocarbon of unknown structure has the formula C8H10. On catalytic hydrogenation over the Lindlar catalyst, 1 equivalent of Η2 is absorbed. On hydrogenation overa palladium catalyst, 3 equivalents of Η2 are absorbed. (a) How many degrees of unsaturation are present in the unknown structure? (b) How many triple bonds are Present? (c) How many double bonds are present? (d) How many rings are present? (e) Draw a structure that fits the data.The conversion of 3 alcohols into alkenes under acidic conditions involves two cationic intermediates. For each reaction, draw the complete mechanism using curved arrows.Draw the major product of this reaction. Ignore inorganic byproducts. 1. LiAIH4 2. Neutralizing work-up
- For the following five reactions, draw the product(s) obtained from the cycloalkene and the reactant cocktails.Please draw the structures for E and F and indicate synthesis steps by arrows that show the reaction direction.the product is given predict from what alkene reactant be made from, write the complete reaction on a sheet of paper A.oxidation of 2-methyl-3-pentanol B.aldol condensation of CH3CH(Br)CHO A.
- dedcue the major organic product from the following reations. be ablw to draw hydration halogenation hydrohalogenation, halohydrin formation, oxymercuratiom demercuration qnd hydroboration oxidation.cpredict the product of the following reactions of aldehyde and ketonePlease draw the structures for C and D and indicate synthesis steps by arrows that show the reaction direction.