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


Sulfuric acid is very corrosive, Chromium compounds are toxic.
Experiment for a chemistry teacher. Use a tray. Do not forget goggles!
An indirect redox reaction of alcohol with dichromate/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  dichromate solution. Add 1 drop of sulfuric acid and mix.
Observation left photo: The orange colour (dichromate ions left) disappears, a blueish colour of chrome ions (right) can be seen, 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, dichromate ions being the  electron acceptors. Alcohol is oxidised leaving aldehyde, dichromate is reduced to chromium ions:

3 CH3CH2OH(l) + Cr2O72-(aq) + 8 H+(aq) ---> 3 CH3CHO(l) + 2 Cr3+(aq) + 7 H20(l)
The aldehyde is volatile as hydrogen bondings are week. It is indicated by the read colour.
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