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- Predict the products obtained from the reaction of triolein with the following reagents.(a) NaOH in water (b) H2 and a nickel catalyst (c) Br2 in CCl4Predict the products obtained from the reaction of triolein with the following reagents.(a) NaOH in waterPredict the products of self-condensation of the following esters.(a) methyl propanoate + NaOCH3 (b) ethyl phenylacetate + NaOCH2CH3
- Predict the products obtained from the reaction of triolein with the following reagents.(a) NaOH in water (b) H2 and a nickel catalyst (c) Br2 in CCl4(d) ozone, then dimethyl sulfide (e) warm KMnO4 in water (f) CH2I2>Zn(Cu)whats the product of acid hydrolysis of the following ester with HClPredict the products obtained from the reaction of triolein with the following reagents. ) CH2I2>Zn(Cu)
- When a molecule has two esters, it can react via an intramolecular Claisen condensation. This is called a Dieckmann condensation. what would be the products of the following reaction (hint: what is going to happen to the protecting group in dilute aqueous acid?).The Principle of Microscopic Reversibility states that a forward reaction and a reversereaction taking place under the same conditions (as in an equilibrium) must follow thesame reaction pathway in microscopic detail. The reverse of the Fischer esterificationis the acid-catalyzed hydrolysis of an ester. Propose a mechanism for the acid-catalyzedhydrolysis of ethyl benzoate, PhCOOCH2CH3Predict the products obtained from the reaction of triolein with the following reagents.(a) NaOH in water (b) H2 and a nickel catalyst
- Predict the products formed when cyclohexanone reacts with the following reagents.excess CH3OH, H+Predict the products of the reaction of phenylaceetaldehyde , C6H5CH2CHO, with a. NaBH4 the H3O+ b. Aqueous acidic CrO3 c. NH2OH d.CH3MgBr then H3O+ e, CH3OH,H+ catalystWhat is the structure and molecular shape of the carboxylic acid obtained from the basic hydrolysis of the following nitrile CH3CH2CN?