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- 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.Which products in Problem 20.28 will produce methyl cyclohexylmethanoate when treated with NaOCH3?Draw the products 1. (S)-2-chlorobutane and sodium acetate in DMSO 2. 1-bromopropane and methylamine in acetonitrile.
- Fill in the blank: The acid catalyzed hydration of alkenes (addition of H2O/H2SO4) is: A) a polar mechanism with carbocation intermediate B) a radical mechanism with carbon radical intermediate C) a concerted reactionFill in the blank: The reaction of alkene with peroxyacid (RCO3H) is: A) a radical mechanism with carbon radical intermediate B) a concerted reaction C) a polar mechanism with carbocation intermediateWhich is ethanal? Question 20 options: HCHO CH3CHO CH3CH2CH2CHO CH3OH
- draw the carbon containing products of the following reaction: Reactant = 2-bromo-4-methyloctane Reagent = O H minus, heatQUESTION 4Predict the products(s) from the reaction of 1-hexyne with each of the following reagents:a) 1 mole of HBrb) H2O, H2SO4, HgSO4c) 2 moles of Br2d) Excess Cl2e) 2 moles of HCl with H2O2f) 1 mole of HClI 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.
- Draw the organic product(s) formed upon the addition of HBr to (a) 2-methyl-2-pentene, (b) trans-2-hexene, and (c) 4-methylcyclohexene. How many regioisomers can be formed in each case?7. Step 1: In this reaction of an alkene with H2SO4 as a reagent, the reactive species is a)H30+ B)HSO4- C)H2O. This is a(n) a)hydrogenation b)acidification c)hydration reaction, and its mechanism is a)nucleophilic substitution b)electrophilic addition c)nucleophilic addition. This reaction produces a)carboxylic acids b)alcohols c)ethers Step 2: Determine which of the two products is the major product. Select the single best answer. A OR Bwhat starting materials and reagents could form the indicated product ? Fill in the reaction, acco unt for H indicated as being from the reaction 1.2.3.4.5