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Lead I by the Dithizone Method

Theory In solution, dithizone (diphenylthiocarbazone) exhibits tautomerism as shown below  [Pg.404]

The enol-ioxm of Dithizone (I) behaves as monoprotic acid having a dissociation constant pKa = 4.7 upto a pH range of about 12 obviously, the acid proton is inherited due to the thiol moiety in (I). In reality, two kinds of metal dithizonates are invariably formed, namely  [Pg.404]

They are of greater analytical value because of their high stability and greater solubility in organic solvents. [Pg.404]

The poor stability and miserable solubility in organic solvents render these products of insignificant analytical importance. [Pg.404]

however, pertinent to mention here that dithizone is an extremely sensitive reagent and, therefore, helps in the determination of lead either from a neutral or faintly alkaline medium to the extent of a few micrograms. [Pg.405]


See other pages where Lead I by the Dithizone Method is mentioned: [Pg.393]    [Pg.403]    [Pg.404]   


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