Predict the oxidation product of treating the given alkene with a peroxyacid reagent. Omit byproducts
In organic chemistry, alkenes are unsaturated hydrocarbons with at least one carbon-carbon double bond present in their structure. Alkenes are more reactive due to the presence of -bonds. Alkenes undergo addition reactions, oxidations and polymerization, and so forth. On reacting with an oxidizing agent, an alkene forms a bond.
Peroxy acid: The peroxy acid is also known as peracid. The name “per” is used before the acid due to the presence of bond and oxyacid is due to the presence of bond. The peracid exhibits electrophilic properties.
Example:
Epoxidation of alkenes:
Epoxides are cyclic ethers with three membered rings. Alkenes on reaction with peroxy acids produce epoxides.
The structure of the reactant and reagent is depicted below:
Mechanism is given below:
Ans:The oxidation product of treating the given alkene with a peroxyacid reagent is given below:
Predict the oxidation product of treating the given alkene with a peroxyacid reagent. Omit byproducts
Predict the oxidation product of treating the given alkene with a peroxyacid reagent. Omit byproducts.
Predict the oxidation product of treating the given alkene with a peroxyacid reagent. Omit byproducts.
Predict the oxidation product of treating the given alkene with peroxyacid reagent. Omit byproducts.
Predict the oxidation product of treating the given alkene with a peroxyacid reagent. Omit byproducts.
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Predict the oxidation product of treating the given alkene with a peroxyacid reagent.
Predict the oxidation product of treating the given alkene with the reagent shown below. Include stereochemistry where applicable. Include H's on chirality centers. (mCPBA = mefa-chloroperoxybenzoic acid)
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