Concept explainers
Interpretation:
The mechanism for the given reaction has to be proposed.
Concept Introduction:
Ring-opening of
Acid-catalyzed ring-opening of epoxide: The epoxide ring is protonated and the nucleophile attack depends on the electronic or steric effect (nature of epoxide).
Regiochemistry: When the epoxide is unsymmetrical, the nucleophile attack at the more substituted position of the protonated epoxide ring.
Stereochemistry: when the nucleophile attack takes place at chiral center, an inversion of configuration is obtained.
Base catalyzed ring opening of epoxide:
The nucleophile will attack at the less substituted position under basic conditions.
Want to see the full answer?
Check out a sample textbook solutionChapter 9 Solutions
Essential Organic Chemistry, Global Edition
- Aldehydes and ketones react with thiols to yield thioacetals just as they react with alcohols to yield acetals. Predict the product of the following reaction, and propose a mechanism:arrow_forwardClaisen rearrangement of an allyl phenyl ether with substituent groups in both ortho positions leads to the formation of a para-substituted product. Propose a mechanism for the following rearrangement.arrow_forwardPropose a detailed mechanism for the following reaction: HO ye OH H₂SO4arrow_forward
- Which compound below could not be made starting from a carbonyl compound under basic conditions (a) HO OH HO OH OH HO OH OHarrow_forwardReaction of phenol with acetone in the presence of an acid catalyst gives a compound known as bisphenol A, which is used in the production of epoxy and polycarbonate resins (Section 29.5). Propose a mechanism for the formation of bisphenol Aarrow_forwardWhat carbonyl compound was used to synthesize the product shown below? س ملام ز ز O O HO OH O methanol and ethanolarrow_forward
- Propose a plausible mechanism for the following transformation: 1) Excess MeMgBr 2) H₂O HO OHarrow_forwardPredict the product(s) and propose a mechanism for the following reaction. LOH H₂SO4 Heatarrow_forwardThe following compound undergoes Benzilic Acid Rearrangementto yield a hydroxyacid salt. Propose a mechanism for the reaction, write the major product, and provide an explanation as to the preference of migration of one R group over the other.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning