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JEE Main 2026 Preparation: Question Papers, Solutions, Mock Tests & Strategy Unacademy » JEE Study Material » Chemistry » Idoform Reaction

Idoform Reaction

Iodoform that is also known as Triiodomethane is a crystalline yellow chemical that belongs to the organic halogen group. Halogens are any of the 6 nonmetallic elements in Group 17 of the periodic table. Fluorine, chlorine, bromine, iodine, astatine, and Tennessee are the halogen elements.

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In the year 1822, George Simon Serullas published the first description of iodoform production. Iodine vapour reactions with steam over red hot coals and potassium response with ethanolic iodine in water were responsible for the synthesis’s appearance. Solutions containing acetone, inorganic iodides, and sodium carbonate produces iodoform in electrolysis aqueous. Several chemicals convert iodoform to methylene iodide, a thick liquid that is blue when pure but discoloured by residues of iodine, and is utilised as a heavy medium in gravity separation procedures. In 1880, the antibacterial qualities of iodoform were discovered, and it quickly became a valuable medical tool. However, more effective drugs have now taken its place.

What exactly is iodoform? 

Iodoform is a crystalline yellow chemical that belongs to the organic halogen group. Triiodomethane is another name for it. You might be wondering what a halogen is. Halogens are any of the 6 nonmetallic elements in Group 17 of the periodic table. Fluorine, chlorine, bromine, iodine, astatine, and Tennessee are the halogen elements. The organoiodine substance iodoform has the formula CHl3. It has a deep and unmistakable fragrance and is a light yellow, crystalline, volatile material.

Test for Iodoform

The iodoform test is used to determine if a certain unknown chemical contains carbonyl compounds with the structure R-CO-CH3 or alcohols with the structure R-CH(OH)-CH3.

 A methyl ketone reacts to produce a yellow precipitate with an “antiseptic” odour and iodine is a base. select a few secondary alcohols with at least one methyl group in the alpha position also test positive.

Using a solution of iodine and sodium hydroxide

Chemically, this is a much more evident technique. A little quantity of aldehyde or ketone is added to an iodine solution, which is then removed with just enough sodium hydroxide solution to eliminate the iodine’s colour. If nothing happened in the cold, the combination may need to be slowly warmed. The development of a very pale yellow precipitate of triiodomethane (formerly known as iodoform) – CHI3 – indicates a favorable result. In Spite of this theory  this is differentiated by a vaguely “medical” Fragrance. It’s utilised as an antibacterial in things like the sticky plasters you apply on small wounds.

Solution of potassium iodide and sodium chlorate(I)

Sodium hypochlorite is another name for sodium chlorate(I). The Potassium iodide solution is added to a tiny quantity of aldehyde or ketone, followed by sodium chlorate(I) solution. If no precipitate forms when the combination is cold, it may be required to carefully warm the mixture. The favourable outcome is just the same pale yellow precipitate that was previously seen.

Description of the Iodoform Test

A pale yellow precipitate of iodoform or triiodomethane is generated if iodine and sodium hydroxide are added to a molecule that includes whether It’s a methyl ketone or a secondary alcohol  in the alpha position with the methyl group. It could be used to distinguish between aldehydes and ketones. Because acetaldehyde is the only aldehyde containing a CH3C=O group, if an aldehyde produces a positive iodoform test, it must be acetaldehyde. 

Mechanism of Iodoform Testing

Firstly, an acidic alpha hydrogen is avoided by the Hydroxide ion. As a result enolate ions are formed by this reaction. And it, an iodide ion displaced the enolate anion from the iodine molecule. R-CO-CI3 is obtained by repeating this method again. A hydroxide ion is now bonded to the carbonyl carbon. The carbonyl group is formatted, and the CI3-  anion is eliminated as a result. Their R-COOH group is also formed. The basic CI3- ion and the carboxylic acid group cancel one another out. Iodoform is produced as a result. As a result, the pale yellow iodoform precipitate is generated, which is distinguished by its unique “antiseptic” odour. 

Iodoform Characteristics 

Let’s look at a few of the properties of iodoform presently. 

1. LIodoform is made via electrolysis of an aqueous solution comprising acetone, inorganic iodides, and sodium carbonate. 

2. Tri-iodomethane is another name for iodoform. The other importance lies in the fact that the chemical contains three iodine molecules.

3. The other importance lies in the fact that the chemical contains three iodine molecules. 

4. It’s a participant of the organic halogen family and an organic iodine chemical.

5. CHI3 is its chemical formula. 

6. It is highly combustible

7. It’s a crystalline pale yellow material.

Conclusion 

Iodoform is a crystalline yellow chemical that belongs to the organic halogen group. Several chemicals convert iodoform to methylene iodide, a thick liquid that is blue when pure but discoloured by residues of iodine, and is utilised as a heavy medium in gravity separation procedures. The iodoform test is used to determine if a certain unknown chemical contains carbonyl compounds with the structure R-CO-CH3 or alcohols with the structure R-CH –CH3. A little quantity of aldehyde or ketone is added to an iodine solution, which is then removed with just enough sodium hydroxide solution to eliminate the iodine’s colour.

faq

Frequently asked questions

Get answers to the most common queries related to the JEE Examination Preparation.

What exactly is a keto methyl group?

Ans: A methyl ketone is a ketone in which one of the carbonyl carbon ligands is a methyl group.  ...Read full

What is the purpose of iodoform as an antiseptic?

Ans: Iodoform can be used as an antiseptic to treat skin infections, ulcers, bruises, boils, and burns, among other ...Read full

How is iodoform made?

Ans: A pale yellow precipitate of iodoform or triiodomethane is generated when iodine and sodium hydroxide are added...Read full

What is the haloform reaction, and what is an example of it?

Ans: The haloform reaction is the reaction of a methyl ketone with chlorine, bromine, or iodine in the presence of h...Read full

Which of the following will not pass the haloform test?

Ans: The haloform reaction will not occur with diethyl ketone. Acetaldehyde and all ketones possessing a CH3CO- grou...Read full

Ans: A methyl ketone is a ketone in which one of the carbonyl carbon ligands is a methyl group.

 

Ans: Iodoform can be used as an antiseptic to treat skin infections, ulcers, bruises, boils, and burns, among other things. When iodoform is applied to the skin, it decomposes and releases iodine. The true antiseptic, iodine, is responsible for eliminating germs and fungus.

Ans: A pale yellow precipitate of iodoform or triiodomethane is generated when iodine and sodium hydroxide are added to a molecule containing either a methyl ketone or a secondary alcohol with a methyl group in the alpha position.

Ans: The haloform reaction is the reaction of a methyl ketone with chlorine, bromine, or iodine in the presence of hydroxide ions to produce a carboxylate ion and a haloform.

Ans: The haloform reaction will not occur with diethyl ketone. Acetaldehyde and all ketones possessing a CH3CO- group exhibit the haloform reaction.

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