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Exercises · 8.25

Q.Why is nitric acid added to sodium extract before adding silver nitrate for testing halogens?

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Nitric acid neutralises excess sodium cyanide and sodium sulphide in the Lassaigne extract, preventing false precipitation with silver nitrate; only then can AgNOX3\ce{AgNO3} selectively detect halide ions as their characteristic silver halts.

Why the Lassaigne Test Needs Nitric Acid First

When we fuse an organic compound with sodium metal, we break it down and convert heteroatoms into water-soluble ionic forms. Nitrogen becomes cyanide (CNX−\ce{CN^-}), sulphur becomes sulphide (SX2−\ce{S^{2-}}), and halogens become halide ions (XX−\ce{X^-}). The resulting alkaline solution—the sodium extract—contains all these anions together.

Silver nitrate is our reagent of choice for detecting halogens because it forms distinct, coloured precipitates with halide ions:

AgX++XX−→AgX↓\ce{Ag^+ + X^- -> AgX v}

where AgCl\ce{AgCl} is white, AgBr\ce{AgBr} is pale yellow, and AgI\ce{AgI} is bright yellow. But here's the problem: silver ion is promiscuous. It doesn't just precipitate with halides.

The Interference Problem

If you add silver nitrate directly to the alkaline sodium extract, you'll see precipitates even when no halogens are present. Two culprits are responsible:

  1. Silver cyanide from nitrogen

AgX++CNX−→AgCN↓\ce{Ag^+ + CN^- -> AgCN v}

White precipitate, easily mistaken for AgCl\ce{AgCl}.

  1. Silver sulphide from sulphur

2 AgX++SX2−→AgX2S↓\ce{2Ag^+ + S^{2-} -> Ag2S v}

Black precipitate that masks everything else.

Both give false positives. You'd conclude halogens are present when they're not, or you'd miss them entirely under a black curtain of AgX2S\ce{Ag2S}.

Watch out

Adding AgNOX3\ce{AgNO3} directly to the sodium extract will precipitate AgCN\ce{AgCN} and AgX2S\ce{Ag2S}, leading to incorrect conclusions about halogen presence.

How Nitric Acid Solves This

Nitric acid does two things before we test for halogens:

1. Neutralises the alkaline extract

The sodium extract is strongly basic (from excess NaOH\ce{NaOH} and NaX2COX3\ce{Na2CO3} formed during fusion). Acidifying it prevents side reactions and prepares the medium for selective precipitation.

2. Destroys interfering anions

NaCN+HNOX3→NaNOX3+HCN↑\ce{NaCN + HNO3 -> NaNO3 + HCN ^}

Hydrogen cyanide is volatile and escapes. No more cyanide means no AgCN\ce{AgCN} precipitate.

NaX2S+2 HNOX3→2 NaNOX3+HX2S↑\ce{Na2S + 2HNO3 -> 2NaNO3 + H2S ^}

Hydrogen sulphide gas is released (you'll smell rotten eggs). No sulphide remains to form black AgX2S\ce{Ag2S}. …

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