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 org11 Aldehyde by direct oxidation of alcohol by permanganate/sulfuric acid


Sulfuric acid is very corrosive, Chromium compounds are toxic.
Experiment for a chemistry teacher. Use a tray. Do not forget goggles!

<--- The photos were done using potassium dichromate in earlier times when the
high cancinogen potential was not yet known.
Now the use of potassium dichromate for chemistry experiments is forbidden.
So potassium dichromate has to be replaced by potassium permanganate.

An indirect redox reaction of alcohol with permanganate/sulfuric acid was already done to produce electricity in a Galvanic Cell.
Now you will mix the three components in a small stoppered bottle. Now you can smell the volatile product and test it by an indicator: "Alcoholus dehydrogenatus" = alcohol which was deprived from hydrogen = aldehyde.

* Mix 1 drop of  methylated spirit and 2 drops of diluted potassium  permanganate solution. Add 1 drop of sulfuric acid and mix.
Observation
The pink colour of permanganate disappears, a smell characteristic for acetaldehyde (ethanal) appears.
Right photo: Add colourless solution of fuchsin sulfurous acid to a piece of tissue paper, fix it in the vial by the stopper: The red colour indicates gaseous aldehyde.
Explanation
Alcohol molecules are the electron donors in this direct redox reaction, permanganate ions being the  electron acceptors. Alcohol is oxidised leaving aldehyde, permanganate is reduced to manganese ions:

5 CH3CH2OH(l) + 2 MnO4-(aq) +6 H+(aq) --->5 CH3CHO(l) + 2 Mn2+(aq) +8 H20(l)
The aldehyde is volatile as hydrogen bondings are week. It is indicated by the read colour.
back....... go on......................first publication: 23.10.2001............................................last modification: 20.01.2012