Sigma Percentile
JEE Main 2014
LEVELJEE Main

Animated Solution for Chemistry - Organic Chemistry: For the estimation of nitrogen, of an organic compound was digested by Kjeldahl's method and the evolved ammonia was absorbed in of sulphuric acid. The unreacted acid required of sodium hydroxide for the complete neutralization. The percentage of nitrogen in the compound is

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Visualized Solution

\text{Kjeldahl's Method Overview}

  • Total is split into two parts:
  • Reacts with evolved
  • Unreacted acid is titrated with

\text{Initial Moles of } H_2SO_4

\text{Moles of } NaOH \text{ Used}

\text{Unreacted } H_2SO_4

  • Reaction:

\text{Reacted } H_2SO_4

\text{Moles of } NH_3 \text{ Evolved}

  • Reaction:

\text{Mass of Nitrogen}

\text{Percentage of Nitrogen}

\text{The Way Forward}

  • What if the compound contained a nitro group () or nitrogen in a ring (e.g., Pyridine)?
  • Kjeldahl's method fails for these as they don't convert to easily.

The Sigma Insight: Nomenclature and Characterisation

Solution Diagram
Quantitative analysis in organic chemistry often feels like solving a mystery. You have an unknown compound, and you need to find out exactly how much of a specific element is hiding inside it. Kjeldahl's method is a classic, elegant technique used to estimate the amount of nitrogen in an organic compound.
Instead of measuring the nitrogen directly, we force it to reveal itself by converting it into ammonia gas (). But ammonia is a slippery, volatile gas. If we try to measure it directly, some of it will escape. So, we use a clever trick called back-titration. We trap the ammonia in a known, excess amount of a strong acid, like sulfuric acid (). Then, we measure how much acid is left over to figure out how much acid reacted with the ammonia.

The Initial Setup

How Much Acid Do We Have?
Our first step is to determine the total amount of sulfuric acid we started with. We are given of (which means ) .
To find the millimoles (mmol), we simply multiply the molarity by the volume in milliliters:
So, we have a total pool of of sulfuric acid waiting to trap the ammonia.

The Back-Titration

Finding the Leftovers
After the ammonia has bubbled through and reacted with the acid, some acid remains unreacted. To find out how much, we titrate this leftover acid with a strong base, sodium hydroxide (). We used of .
Let's calculate the millimoles of used:
Now, we must be very careful with the stoichiometry. The neutralization reaction is:
Notice that it takes two moles of to neutralize just one mole of . Therefore, the of we used must have neutralized exactly half that amount of sulfuric acid:

The Core Reaction

Unmasking the Ammonia
If we started with of acid and was left over, the amount that actually reacted with the ammonia is simply the difference:
Now, let's look at the reaction between ammonia and sulfuric acid:
Here, one mole of can trap two moles of . Since of acid reacted, it must have trapped twice as much ammonia:

The Final Percentage

Every single molecule of ammonia () contains exactly one atom of nitrogen. Therefore, of ammonia means we have of nitrogen atoms.
Let's convert these millimoles into mass. The atomic mass of nitrogen is .
Finally, to find the percentage of nitrogen in the original organic compound, we divide the mass of nitrogen by the total mass of the compound () and multiply by :
And there we have it! The compound contains exactly nitrogen. While Kjeldahl's method is incredibly powerful, always remember its limitations: it struggles with compounds where nitrogen is in a ring (like pyridine) or in nitro/azo groups, as they don't easily convert to ammonium sulfate during digestion.

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