Sigma Percentile
LEVELJEE Advanced

Animated Solution for Chemistry - Organic Chemistry: An organic compound having molecular mass 60 is found to contain C = 20%, H = 6.67% and N = 46.67% while rest is oxygen. On heating, it gives alongwith a solid residue. The solid residue gives violet colour with alkaline copper sulphate solution. The compound is

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Visualized Solution

The Sigma Insight: Amines

Solution Diagram
The journey of identifying an unknown organic compound is much like being a detective at a crime scene. You are given a set of clues—percentages, masses, and chemical behaviors—and your job is to piece them together to reveal the true identity of the molecule.
In this problem, we are handed a classic analytical chemistry puzzle. We have the percentage composition of Carbon, Hydrogen, and Nitrogen, along with the molecular mass. But the final nail in the coffin is a beautiful, colorful chemical reaction. Let's dive into the investigation!

Analyzing the Setup

The Percentage Composition
Our first piece of evidence is the elemental composition. The problem states that the compound contains Carbon, Hydrogen, and Nitrogen.
But wait, there is a missing piece! The problem mentions that the "rest is oxygen." In elemental analysis, oxygen is often the silent partner. It is notoriously difficult to measure directly in combustion analysis, so we always find it by difference.

The Master Equation

Finding the Missing Oxygen
Since the total percentage of all elements in any compound must perfectly sum up to , we can easily find the percentage of oxygen. We simply subtract the sum of the known percentages from .
Let's substitute our known values into this logical framework:
Now we have the complete elemental profile of our mystery compound!

The Mole Concept

Decoding the Empirical Formula
Percentages are great, but atoms react in whole numbers, not percentages. To find the true ratio of atoms, we need to convert these mass percentages into relative moles.
How do we do this? We divide the percentage of each element by its respective atomic mass. This normalizes the data, allowing us to compare apples to apples.

The Simplest Ratio

Building the Skeleton
We now have the relative number of moles, but they are in messy decimals. Molecules demand elegant, whole-number ratios. To find the simplest whole-number ratio, we divide all the molar values by the smallest value among them, which is .
For Carbon:
For Hydrogen:
For Nitrogen:
For Oxygen:
This beautiful, clean ratio gives us our Empirical Formula: .

The Molecular Formula

The Final Identity
The empirical formula is just the simplest ratio. Is it the actual molecule? To find out, we must compare the empirical mass with the given molecular mass.
Let's calculate the mass of our empirical formula:
The problem explicitly states that the molecular mass of the compound is . Since the empirical mass perfectly matches the molecular mass, the multiplier is exactly .
Therefore, our Molecular Formula is also .

The Chemical Confession

The Biuret Test
Now, we must identify the specific compound. The formula corresponds to Urea, which is structurally written as .
But the problem gives us a final, undeniable confirmation. It states that on heating, the compound releases ammonia gas () and leaves behind a solid residue. When this residue is treated with an alkaline copper sulphate () solution, it produces a striking violet color.
This is the legendary Biuret Test! It is a classic qualitative test for peptide bonds. When two molecules of urea are heated, they condense, eliminating a molecule of ammonia to form a compound called Biuret.
The resulting Biuret molecule forms a complex with the ions in the alkaline solution, resulting in that signature violet hue.
This chemical behavior perfectly aligns with our mathematical derivation, confirming beyond a shadow of a doubt that our mystery compound is indeed Urea.

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