A number of functional groups are well tolerated under the reaction conditions.
Hydrolysis of vinyl ether mechanism.
Furthermore the reaction enables a facile entry to labile diarylacetaldehydes by tfa mediated hydrolysis of the β β disubstituted vinyl ethers.
As has been pointed out by some comments your proposed mechanism is not really possible.
Synthesis and mechanism of acidic hydrolysis of cis and trans 10 2 phenylvinyl phenothiazines.
Hydrolysis of vinyl ether for jee main guruprakashacademy.
Identify allyl vinyl.
Rates of hydrolysis of cis and trans β phenylvinyl methyl ethers cis and trans β p nitrophenyl vinyl methyl ethers and cis and trans β cyanovinyl ethyl ethers were measured in concentrated 10 55 wt aqueous perchloric acids the results show that these cis and trans isomers do not interconvert under the hydrolysis reaction conditions and that formation of the alkoxy carbonium ion.
Ester hydrolysis reaction mechanism.
The general structure is r 2 c cr or where r h alkyl or aryl a common subfamily of enol ethers are vinyl ethers with the formula roch ch 2 important enol ethers include the reagent 3 4 dihydropyran and the monomers methyl vinyl ether and ethyl vinyl ether.
From what i can tell you are having more trouble with the acidic hydrolysis of an enol ether to an aldehyde.
The two methods give identical rate constants.
Chem 2013 78 9815 9821.
The kinetics of the acid catalysed hydrolysis of ethyl vinyl ether in aqueous solution have been measured by following the disappearance of the ether and by following the appearance of acetaldehyde.
In organic chemistry an enol ether is an alkene with an alkoxy substituent.
For reproduction of material from njc.
The reaction is first order in ethyl vinyl ether and first order in hy.
The journal of organic chemistry 1997 62 22.
The facile general acid catalyzed conversion of 2 ethoxy 1 cyclopentene 1 carboxylic acid to cyclopentanone.
Vinyl mathrm sp 2 cations are very unstable and an mathrm s n1 type dissociation of meoh is very unlikely.
Methyl vinyl ether is an organic compound with the chemical formula ch 3 och ch 2 a colorless gas it is the simplest enol ether it is used as a synthetic building block as is the related compound ethyl vinyl ether a liquid at room temperature.