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In Lassaigne's test, organic elements are converted to ionic forms by fusion with sodium metal: N → NaCN, S → Na2S, halogen → NaX.
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When both nitrogen AND sulfur are present together, NaSCN (sodium thiocyanate) is formed instead of separate NaCN and Na2S.
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FeCl3 gives Prussian blue only when nitrogen alone is present (as NaCN); with both N and S (as NaSCN), it gives blood-red Fe(SCN)3.
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Before the AgNO3 halogen test, the Lassaigne extract must be boiled with dilute HNO3 to destroy NaCN and Na2S which would otherwise cause interference.
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AgCl is white and soluble in dilute NH3; AgBr is pale yellow and partially soluble in concentrated NH3; AgI is yellow and insoluble in NH3 at any concentration.
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The 2,4-DNP test detects any carbonyl (C=O) group but cannot distinguish aldehydes from ketones; Tollens' test is needed for that distinction.
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The iodoform test (I2/NaOH → yellow CHI3) is specific for methyl ketones (CH3CO-R) and does not work with non-methyl ketones like 3-pentanone.
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The KMnO4/oxalic acid titration is self-indicating (no external indicator needed), requires 60–70 °C, and the balanced equation is 5C2O42- + 2MnO4- + 16H+ → 10CO2 + 2Mn2+ + 8H2O.
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Acetanilide is prepared by acetylation of aniline with acetic anhydride and is used as a protected amino compound for selective para-nitration in synthesis.
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The carbylamine test (CHCl3 + KOH → foul isocyanide) is specific for primary amines (-NH2) only; secondary and tertiary amines give negative results.
Part of OC-10 — Practical Organic Chemistry
Practical Organic Chemistry: Ten Core Statements
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