A Secondary Alcohol When reduced with something like lithium aluminum hydride, a ketone results in a secondary alcohol.
Reduction of a ketone lead to a secondary alcohol.
A secondary alcohol.
You usually reduce a ketone such as propanone using sodium borohydride to propanol.
Wolff-Kishner reaction is used in order to reduce a ketone to an alkane. NH2NH2 (hydrozine) and KOH are used in the reaction.
Ketone
ketone
Mild oxidation of a secondary alcohol will produce a ketone; strong oxidation, such as burning, can produce carbon dioxide and water.
You usually reduce a ketone such as propanone using sodium borohydride to propanol.
Ketoacidosis
The result is the production of ketone bodies
Wolff-Kishner reaction is used in order to reduce a ketone to an alkane. NH2NH2 (hydrozine) and KOH are used in the reaction.
Ketone
methyl ethyl ketone
ketone
I) 1) Reduce with NaBH4, then 2) a weak acid workup. II) Tert-butoxide and heat III) Hydroboration IV) Na2Cr2O7, HCl
Mild oxidation of a secondary alcohol will produce a ketone; strong oxidation, such as burning, can produce carbon dioxide and water.
This is actually an organic chemistry question, but it is a Methyl Ketone.
Litmus strips estimate the pH of a solution. Ketone strips detect the presence of ketone bodies in the solution. Specifically, ketone strips are more sensitive for acetoacetate and less so for beta hydroxybutyric acid.
Hydrogen Peroxide H2O2 and Superoxide O2-