Propose a mechanism for acid-catalyzed acetal formation between propiophenone and ethylene glycol. 5. Propose a mechanism...
Provide a detailed, stepwise mechanism for the acid-catalyzed reaction of 2-butanone with ethylene glycol (HOCH2CH2OH) to produce an acetal. HC. CH HCL HOSH HCC oc 다
Provide a detailed, stepwise mechanism for the acid-catalyzed reaction of 2-butanone with ethylene glycol (HOCH_2CH_2OH) to produce an acetyl.
Draw the reaction mechanism for the formation of hemiacetal and the acetal in the acid-catalyzed reaction of propanone with ethanol
Draw the full mechanism (using arrows) of the formation of the cyclic acetal when 5-hydroxy-3-methylheptanal reacts with one molecule of ethylene glycol in acidic conditions. First, a hemi-acetal will form, and then the cyclic acetal will form.
1. show the complete mechanism for the protection of cyclopent-2-enone as an acetal using ethylene glycol as the alcohol component 2. starting with 2-cyclopentenone and any alcohols of 4 carbons or less, show how you would synthesize isopropyl 3- ethylcyclopentanecarboxylate.
1. Show the complete mechanism for the protection of cyclopent-2-enone as an acetal using ethylene glycol as the alcohol component. 2. Starting with 2-cyclopentenone and any alcohols of 4 carbons or less, show how you would synthesize isopropyl 3-ethylcyclopentanecarboxylate.
Bonus: Draw a mechanism for the formation of the product in the acid-catalyzed reaction below. (0-5 pts) H-CI OH
Write the mechanism for the reaction of propanal reacting with ethylene glycol, p-toluenesulfonic acid, benzene. h) 0 p-toluenesulfonic acid, Eenzene Fropanal Ethyłe re glycol 0 2-Ethyil-[1,3]dioxolane
Propose a mechanism for the acid catalyzed hydrolysis of the following imine.
7. The reaction sh own below illustrates the acid-catalyzed hydrolysis of an acetal into a hemiacetal. H3o* NH Draw the complete arrow pushing mechanism that accounts for products shown above. (8 pts)