Help me draw this *mechanism*please! My acid catalyst is H2SO4 (sulfuric acid) please show me the...
Draw a proposed mechanism for the reaction of cyclohexanol with aqueous sulfuric acid to yield cyclohexene. Label each step as either: nucleophilic attack, loss of a leaving group, or proton transfer. What type of elimination reaction is this: E1 or E2? Explain. Explain how the leveling effect has occurred in this reaction? What is the likely base in the last step: water or HSO4-? Explain.
Draw the mechanism of cyclopentanol reacting with water and sulfuric acid (H2SO4). Is the mechanism E1 or E2?
what is the purpose of the acid catalyst: sulfuric acid? why
cant acetic acid, which is already being used, serve in the same
capacity? show mechanism of the reaction
H+ R-C-OH + carboxylic acid (excess) R2-OH alcohol + HO Ric-o-R₂ an ester The general reaction scheme for a Fischer esterification is shown above. Using the combination of acetic acid and either isopentanol AND n-propanol you will synthesize two fruity-smelling esters. The hydronium source that will catalyze this reaction is sulfuric...
8.(12 pts) Draw the mechanism for the addition of water to the alkene (with acid catalyst) Clearly show the 3-D geometry of the intermediate and be sure to clearly depict (in 3-D) all possible stereoismers that are produced. CH3CH2 H H2SO4 + H2O -CH₃ CHE
a) Draw the mechanism (including electron-movement arrows) of the acid-catalyzed esterification + H2O Sulfuric Acetic acid Isoamyl alcohol acid isoamyl acetatewater (concn.) (glacial)
question 1 and 2 from my lab please
Data: Propyl Acetate: 32 Sulfuric acid-3 drops Weight of Ester 936 Results We were successful in the creation of an ester. We were able to produce propyl acetate after a series of experimentation Our final product weighed 0,96 grams It also gave off the smell of the product "vicks Vapor Rub Post Lab questions I) Draw out the mechanism for you synthess including a transition state. The reaction i nucleophilic acyl substitution...
Acid Catalyzed Hydration-treatment of alkenes with water in the presence of acid catalyst leads to the formation of alcohols. H2SO4/H2O > 150°C Mechanism Major Product Acid catalyzed dehydration goes through a carbocation intermediate. This means that the Markovnikov product is obtained when carbocation rearrangements do not occur. The need for excessively high temperatures makes this reaction of limited use in laboratory synthesis. Oxymercuration - Oxymercuration involves the addition of Hg to the alkene using mercury (II) acetate Hg(OAc) followed by...
please draw the mechanism for this reaction!
Dowex thom Lom Domeniul: no + OH OH ~ + H2O 3-methyl-1-butanol acetic acid isopentyl acetate
3. Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use curved arrows to indicate the flow of electrons. (Note: use hydronium ion, H307, in your mechanism to indicate "acidic water"). (6 pts) 4. Draw a stepwise, detailed mechanism for the reaction below. Use curved arrows to indicate the flow of electrons. (Hint: think of this reaction as a combination of addition of HX (step 1) and hydration (step 2)]. In the second step, an...
Please include labeling of what occurred during each step
Physical Data Draw the reaction mechanism of acetic acid (ethanoic acid) reacting with isopentyl alcohol (3-methyl-1- butanol) to produce isopentyl acetate (3-methyl-1-butyl acetate, product).