The reaction of sodium borohydride with ketones proceeds rapidly at room temperature, forming an intermediate borate ester which is hydrolyzed to give the product alcohol: 4 R2C=O + Na+BH4- ---> (R2CHO)4B-Na+ 2. (R2CHO)4B-Na+ + 2H2O ---> 4R2CHOH + Na+BO2- Rewrite these two steps using benzil as the ketone, and using structural formulas throughout, rather than the condensed forms above. For example, the structural formula for water is H-O-H. Please write them by hand and paste them in.
The reaction of sodium borohydride with ketones proceeds rapidly at room temperature, forming an intermediate borate ester which is hydrolyzed to give the product alcohol: 4 R2C=O + Na+BH4- ---> (R2CHO)4B-Na+ 2. (R2CHO)4B-Na+ + 2H2O ---> 4R2CHOH + Na+BO2- Rewrite these two steps using benzil as the ketone, and using structural formulas throughout, rather than the condensed forms above. For example, the structural formula for water is H-O-H. Please write them by hand and paste them in.
Chapter27: Biomolecules: Lipids
Section27.SE: Something Extra
Problem 47AP: Cembrene, C20H32, is a diterpenoid hydrocarbon isolated from pine resin. Cembrene has a UV...
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- The reaction of sodium borohydride with
ketones proceeds rapidly at room temperature, forming an intermediate borate ester which is hydrolyzed to give the product alcohol: - 4 R2C=O + Na+BH4- ---> (R2CHO)4B-Na+
2. (R2CHO)4B-Na+ + 2H2O ---> 4R2CHOH + Na+BO2-
Rewrite these two steps using benzil as the ketone, and using structural formulas throughout, rather than the condensed forms above. For example, the structural formula for water is H-O-H. Please write them by hand and paste them in.
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