Identification of an organic unknown

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Identification of an organic unknown

Here is the flow chart to determine the unknown organic. Start with the 2,4-DNP test and then follow the chart.

DNP - 2,4-dinitrophenylhydrazine test

The Safety:

• DNP is harmful – avoid contact with skin, eyes etc. Wear safety glasses.

• At this stage we have no idea what the organic chemical to be tested is, so wear gloves.

The Instructions:

To 1cm3 of 2,4-dinitrophenylhydrazine (DNP) solution, add a few drops of the unknown organic

substance.

If a yellow/orange precipitate is formed, it indicates the presence of a carbonyl group (aldehyde or

ketone) (positive result). Move on to the Tollen's reagent test.

If no precipitate is formed (negative result), move on to the Bromine water test.

The Chemistry:

2,4-dinitrophenylhydrazine bonds to carbonyl compounds and makes an orange precipitate. The

reaction also releases water.

Tollen's reagent test

The Safety:

• Silver nitrate is poisonous and harmful, particularly to the eyes and nose. It will stain skin.

• Sodium hydroxide is an irritant when dilute.

• Aldehydes and ketones may be toxic.

• Silver metal poses little threat.

• Ammonia in solution is particularly damaging to the eyes, besides being toxic if swallowed and

harmful to the skin.

• Wear goggles and gloves, avoid contact with chemicals.

The Instructions:

Tollen's reagent must be prepared within a couple of hours of use. Preparation instructions for testing

one chemical:

- Add a drop of dilute NaOH to 1cm3 of AgNO3. A brown precipitate (silver oxide) will form.

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- Add concentrated NH3 until the precipitate just dissolves.

Add a few drops of the carbonyl compound to the prepared Tollen's reagent in a test tube. Leave it in a

hot water bath for a few minutes.

If a "silver mirror" (or merely a silver precipitate) forms on the test tube, it is an indication that an

aldehyde is present (positive).

Otherwise (negative), the unknown chemical is a ketone.

The Chemistry:

Tollen's reagent is an oxidising agent, and will oxidise an aldehyde to a carboxylic acid. Ketones won't

be oxidised.

2Ag(NH3)2+ + R-CHO + 3OH- → 2Ag + R-COO- + 4NH3 + 2H2O

The ...

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