Weeks 48 5: Hydrogenation of methyl oleate to give methyl stearate . Understand the reaction stoichiometry...
I need help with questions 5, 6, & 7. The FTIR and NMR is provided. I also need help creating a reaction mechanism using the following: Starting material: methyl acetate. Solvent: diethyl ether Reagent: sodium methoxide Product: methyl acetoacetate THANK YOU!!!!! 11-8: Claisen Condensation - 1 For this assignment, the target compound that you should synthesize is methyl acetoacetate.This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep...
I need help with questions 5, 6, & 7. The FTIR and NMR is provided. I also need help creating a reaction mechanism using the following: Starting material: 1,7-Dimethyl-heptanedioate Solvent: Diethyl ether Reagent: sodium methoxide Product: 3-oxo-cyclohexane carboxylic acid methyl ester THANK YOU!!!!! Ö 11-11: Dieckmann Reaction For this assignment, the target compound that you should synthesize is 2-oxo-cyclohexane carboxylic acid methyl ester.This is an intramolecular carbonyl addition variation. Examine the product and determine which ester is the nucleophile and...
i need help with the postlab questions please Grignard reagent THE GRIGNARD REAGENT-PREPARATION AND REACTION In this experiment, you will prepare a Grignard reagent, phenyl magnesium bromide, from bromobenzene and magnesium metal. The Grignard reagent will then react with methyl benzoate to form triphenylmethanol. Introduction Grignard reagents, such as organomagnesium halides, were discovered in 1910 by French chemist Victor Grignard. The Grignard reaction is one of the most general methods for carbon- carbon bond formation in all of organic chemistry....