1. Because NaBH4 is a mild reducing agent, it must be used with a protic solvent such as methanol to facilitate the reaction. This results in a side reaction between the borohydride and the methanol resulting in the production of hydrogen gas (the fizzing you observed during the addition of the reagent. Use curly-arrows to show the Bronsted acid-base reaction of one equivalent of BH4 - with methanol.
2. For the reason shown above, a fair excess of sodium borohydride was used. Neglecting the reaction of the borohydride with methanol, what mass of sodium borohydride would be required for complete reaction of 5.10g of vanillin according to the first balance equation above? SHOW YOUR WORK
1. Because NaBH4 is a mild reducing agent, it must be used with a protic solvent such as methanol to facilitate the reac...
Help with explanation of 2, 3 and 4 please?? I. Provide a curved-arrow mechanism for the first step of the reduction of vanillin with borohydride in methanol. Show and explain the role of the protic solvent in the reaction (10%) 2. Balance the reaction of vanillin with sodium bordride shown below (assuming alth borohydride reacts with the cyclohexanone as shown) and the subsequent hydrolysis under acidic conditions. (15%) RH. CON CHR 3. Because NaBes a mild reducing agent, it must...
For the reduction of benzophenone to benzohydrol by NaBH4 1) Draw the reaction, showing the reactants and products. • What apparatus and conditions (solvent, temp., reaction time, etc) will be used for the reaction? (we are using ethanol and Buchner funnel filtration) • How will the benzhydrol product be isolated from the reaction mixture and how will it then be further purified? How will the product be characterized? • Identify which is the reducing agent and which is the oxidizing...
5) Rationalizing the stereochemical outc ome of this reaction requires an understanding of the f borohydride borohydride lcohol. An three-dimensional structure of benzoin and the general reaction mechanism o reductions. As shown previously (10-1), the usual mode of activation tor reduction occurs via an intermolecular H-bond between the carbonyl group and an a intramolecular H-bond can stabilize the lowest-energy conformation of benzoin (pre and serve to activate the carbonyl for reduction, thus generating the lowest-energyt state. a) Draw the lowest-energy,...