the reagents necessary to convert alcohol to ketone which involves oxidation of alcohols.
<h3>What is oxidation of alcohols?</h3>
Alcohol oxidation is a significant organic chemistry process. Secondary alcohols can be oxidized to produce ketones, while primary alcohols can be oxidized to produce aldehydes and carboxylic acids.
In contrast, tertiary alcohols cannot be oxidized without the C-C bonds in the molecule being broken.
In order to cause primary alcohols to oxidize into aldehydes
(dichromate)
/pyridine (Collins reagent)
Chromium pyridinium compound (PCC)
Dichromate of pyridinium (PDC, Cornforth reagent)
Periodinane by Dess-Martin
Oxalyl chloride with dimethylsulfoxide (DMSO) for Swern
oxidation of secondary alcohols to ketones
(dichromate)
/pyridine (Collins reagent)
Chromium pyridinium compound (PCC)
Dichromate of pyridinium (PDC, Cornforth reagent)
Periodinane by Dess-Martin
Oxalyl chloride and dimethyl sulfoxide (DMSO) (Swern oxidation)
/acetone (Jones oxidation)
Acetone with aluminum isopropoxide (Oppenauer oxidation)
To learn more about oxidation of alcohols with the given link
Hydrogen chloride (HCl), a compound of the elements hydrogen and chlorine, a gas at room temperature and pressure. A solution of the gas in water is called hydrochloric acid.