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- Identify the most and the least basic compound in each of the following sets. Leave the remaining answer in each set blank. a) Lithium ethoxide: b) Sodium chloride: c) Sodium acetate: Lithium diisopropylamide: Sodium formate: Sodium methoxide: Lithium acetate: Sodium acetate: Sodium phenoxide:Identify the most and the least basic compound in each of the following sets. Leave the remaining answer in each set blank. a) Lithium ethoxide: v Lithium diisopropylamide: v Lithium acetate: b) Sodium chloride: v Sodium formate: Sodium acetate: c) Sodium acetylide: v Sodium p-nitrobenzoate: Sodium benzoate:( -NH NH Identify the Bronsted base in the following reaction of I and II shown below. НО 11 CF₂ CF₁ A) compound I B) compound II
- Amidation Reactions Part A Learning Goal: To identify characteristics common to all amidation reactions, and to apply these generalities in drawing specific amidation reactants or products. Part B Amidation reactions are condensation reactions. In a condensation reaction, two molecules join with a new covalent bond, and this results from the removal of a small molecule such as a water molecule. The reactants in amidation are a carboxylic acid and an amine, and the products are an amide and a water molecule. The carboxylic acid reactant can be of any type. The amine can be simple ammonia (NH₂). a primary amine. or a secondary amine. It cannot be a tertiary amine because tertiary amines lack the N-H Aspartame, an amide, is the sweetener commonly used in diet cola. COOH CH2 < 33 of 38 Review | Constants | Periodic Table CH2 O H₂N CH C NH-CH-COOCH3 7 H 2D EXP. CONT. aspartame Draw the carboxylic acid that is a reactant in the production of aspartame. Draw the molecule on the canvas by…Please help me with both of these questions, they are related and I am very confusedWhy is the N-H bond of an imide especially acidic? A) The conjugate acid is stabilized by resonance. B) The conjugate base is stabilized by resonance. The conjugate base is stabilized by (c) intramolecular hydrogen bonding. The conjugate base is stabilized by electron- (D donating inductive effect.
- The structure of an ester could either be A or B: CH3 O O CH3 T || -C-OCH3 CH3-C CH3-C-O-C-CH3 CH3 CH3 A B Its ¹H NMR spectrum consists of two peaks at 80.9 and 83.6 (relative areas 3:1). Which compound is it? Describe the spectrum that would be expected if it had been the other ester.4. Propose a synthesis scheme for the amine shown below using the starting material indicated. No mechanisms (electron flow arrows, etc.) are needed! (More than one reaction will be needed to make this amine.) Make: From: NH, and other reagents/reactantsPropose a structural formula for each compound consistent with its 1H-NMR and 13C-NMR spectra.
