In an undergraduate organic experiment, we are required to identify the functional group present via solubility tests (with H2O, HCl, NaOH and NaHCO3) and Classification Tests (Brady's, Tollen's, Iodoform, FeCl3, Aqueous Bromine, Lucas and Chromic Acid Test).
The results:
The unknown is found to be insoluble in all the solvent used in the solubility test. The results from the classification test have also shown that the unknown contains ketone. The IR spectra contains a strong peak at ~1700cm-1 which indicates the presence of a carbonyl (C=O) bond. *IR attached* The preliminary boiling point for the liquid unknown is ~ 212 degree Celsius.
Since it is most probably a ketone, I proceeded with the second part of the experiment (Crystalline derivatives for identification). Other lab mates whose unknowns have been suspected to have ketone/aldehyde managed to form semicarbazone in minutes/seconds. I am rather worried as my liquid unknown took a very long time (hours) to form semicarbazone. Could it be that the unknown has been falsely analysed?