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Reduction of benzophenone to diphenylmethanol mechanism


reduction of benzophenone to diphenylmethanol mechanism

Slowly add, through the condenser, enough 6M HCl to acidify the solution.
Add about 50 mL of water to dissolve the H3BO3 and allow the layers to form.
What do you think the precipitate is?
The opposite of oxidation (discussed earlier reduction reactions can be determined by looking for: a) a loss of oxygen from a bond b) the addition of hydrogen to a bond c) the replacement of a more electronegative atom with a less electronegative atom.Filter off the drying agent and evaporate the ether on a steam bath.What absorptions should/should not appear in the product's IR spectrum?It has a melting point of 69 C and a boiling point of 298.Modafinil 2 and the, benzhydryl group is present in the structure of many histamine.Sodium borohydride is highly caustic and must not come in contact with your skin, eyes, or nasal passages.Here only carbonyl groups are reduced.In pharmaceutical manufacture it preparation concours avenir et puissance 11 is used in the synthesis of antihistamines / antiallergenic agents and antihypertensive agents.3 References edit Retrieved from " ").Set up a dry reflux apparatus as seen on pages 202-203 of the, oclsm. .If you cannot hear rattling, replace the drying agent (calcium chloride) using the method your instructor will demonstrate.You will then characterize it using the techniques you have mastered over the term.
Check the pH with litmus paper (redacidic).
Note: Some boric acid will precipitate upon addition of ether. .




Section.6 of Vollhardt and Schore also covers this topic.RE: What is the mechanism for the reduction of Benzophenone with Sodium Borohydride to produce Diphenylmethanol?Hint: Find the literature value of the melting point of diphenylmethanol and then review the critieria for a suitable recrystallization solvent.Note: Hexanes have a boiling point of just a few degrees higher than the product's melting point. .A more specific reduction method involves hydride (H-) transfer reagents. .Benzhydrol is also used in the production of agrochemicals as well as other organic compounds and as a terminating idee cadeau pour la voiture group in polymerizations.Take a melting point and an IR of your final product to aid in its characterization. .
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Combine the ether layers.




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