The reaction behind the Tollens' test is generally an
alkali-catalysed redox reaction. To create Tollens' reagent, one first adds
concentrated ammonia to aqueous silver nitrate (AgNO3) in slight
excess to create the diamminesilver complex ion, [Ag(NH3)2]+
(aq).
During this procedure, insoluble silver oxide is first
precipitated, and with the addition of excess concentrated ammonia, the silver
oxide is 'ammoniated' to form the soluble silver complex ion, which is
indicated by the re-dissolving of the precipitate. After this, a little aqueous
sodium/potassium hydroxide is added to the reagent as a catalyst, and ammonia
added again to dissolve any precipitate.
Thus, in the reagent we now have an oxidizing agent, which
is the diamminesilver complex ion, and a catalyst, i.e. the hydroxide ion. However,
after a short period of time (roughly a day) the reagent will decompose to form
a very hazardous and extremely shock-sensitive explosive, silver nitride (Ag3N).
Thus, Tollens' reagent should be used immediately after preparation and
disposed of properly after use.
To run the test, one just has to add the organic compound that
is to be tested into the reagent and observe any changes.
For aldehydes, the –CHO group acts as a reducing agent,
reducing the diamminesilver ion to aqueous ammonia, and also elemental silver, which deposits on
the walls of the reaction vessel to form a silver mirror. In the process, the
aldehyde is oxidized to the corresponding carboxylic acid.
Overall redox reaction
For ketones, however, the C=O group cannot reduce the diamminesilver ion, and no reaction occurs.
Besides analytical purposes, Tollens' reagent was also used
before the advent of electroplating as a means of manufacturing mirrors.
However, due to its hazardous properties this method of production has fallen
out of use.
No comments:
Post a Comment