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Test for Alcoholic (R-OH) Group Procedure, Observations and Results

Last Updated on Jun 10, 2025
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In organic chemistry, the alcoholic group refers to the OH (hydroxyl) group attached to a carbon atom. Compounds that have this group are called alcohols. Alcohols are common in everyday life; they are found in sanitizers, medicines, fuels, and even in perfumes. Chemically, they are important because the OH group can take part in many reactions. 

There are three main types of alcohols, depending on how the OH group is attached

  • Primary alcohol- The OH group is attached to a carbon that is connected to only one other carbon.
  • Secondary alcohol- The carbon with the OH is attached to two other carbon atoms.
  • Tertiary alcohol- The OH group is on a carbon connected to three other carbon atoms.

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Before we use the alcohols in reactions or identify unknown compounds, it’s important to confirm if the OH group is really present. That’s where the tests for alcoholic groups come in. In this article, we’ll learn about simple lab tests that help you detect alcohols easily.

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Why Test for Alcoholic Groups?

Testing for the alcoholic OH group helps us know if a compound is an alcohol. This is an important step in organic chemistry, especially during lab work or when studying unknown substances.

These tests are useful because:

  • They help confirm the presence of alcohols in a sample.
  • They can tell us the type of alcohol Whether it’s primary, secondary, or tertiary
  • They are often used in practical exams, chemical analysis, and research

Knowing how to perform these tests and understand the results is a key skill for students preparing for competitive exams or lab experiments.

Common Test for Alcoholic Group

There are a few easy and reliable tests to check if a substance contains an alcoholic group. These tests are often used in school labs and exams.

Here are some of the most commonly used tests:

  • Lucas Test- Helps identify whether an alcohol is primary, secondary or tertiary based on how fast it reacts.
  • Sodium Metal Test- Detects the OH group by checking if hydrogen gas is released when sodium is added.
  • Esterification Test- Confirms the presence of alcohol by forming a sweet- smelling ester when reacted with an acid.
  • Ceric Ammonium Nitrate (CAN) Test- Shows a colour change if an alcohol is present.

Each test works in a slightly different way, but all help in identifying alcohols quickly and clearly.

Lucas Test:

The mixture of zinc chloride and concentrated hydrochloric acid is known as the Lucas reagent. It reacts with primary, secondary, and tertiary alcohols at different rates. This reagent forms a cloudiness when it reacts with alcohol. Tertiary alcohols react immediately and create cloudiness, secondary alcohols react slowly and create cloudiness after 5 to 10 minutes, and there is no reaction with primary alcohols.

The chemical reactions are shown below.

Note:

  • Immediate cloudiness indicates tertiary alcohols.
  • Cloudiness appearing within five to ten minutes indicates secondary alcohols.
  • Cloudiness appearing only upon heating indicates primary alcohols.

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Materials Required:
  • Sodium metal
  • Acetic acid
  • Ceric ammonium nitrate
  • Acetyl chloride
  • Ammonium hydroxide
  • Iodine
  • Sodium hydroxide
  • Calcium sulfate
  • Lucas reagent (zinc chloride and Con.HCl)
  • Test tubes
  • Test tube holder
  • Filler

Preparation of Reagents:

  • Ceric Ammonium Nitrate: Dissolve 20gm of orange crystals of ceric ammonium nitrate in 200ml of warm dilute nitric acid.
  • Lucas Reagent: Dissolve 135gm of anhydrous zinc chloride in 100ml of concentrated hydrochloric acid.
  • Iodine Solution: Dissolve 5gm of potassium iodide in 40ml of water. To this solution, add 1gm of solid iodine and dissolve it completely.

Sodium Metal Test:

  • Pour the organic compound to be tested into a dry test tube.
  • Add 1gm of anhydrous calcium sulfate and shake well to get rid of excess water.
  • Pour the solution into another clean test tube.
  • Add a small piece of sodium metal.
  • If brisk effervescence appears due to the evolution of hydrogen gas, it indicates the presence of an alcoholic group.

Ester Test:

  • Add 1ml of the organic liquid to be tested to a clean dry test tube.
  • Add 1ml of glacial acetic acid and 2-3 drops of conc. sulfuric acid.
  • Heat the mixture in a water bath for 10 minutes.
  • Pour the hot mixture into a beaker containing cold water.
  • Smell the water in the beaker.
  • A fruity smell confirms the presence of an alcoholic group.

Ceric Ammonium Nitrate Test:

  • Add 1ml of the given compound to a dry test tube.
  • Add a few drops of ceric ammonium nitrate reagent and shake the solution well.
  • Observe the solution.
  • If a red precipitate appears, then the presence of an alcoholic group is confirmed.

Acetyl Chloride Test:

  • Pour 2ml of the given organic compound into a clean test tube.
  • Add 1gm of anhydrous calcium sulfate and shake well.
  • Filter the solution. To the filtrate, add 3 to 4 drops of acetyl chloride and shake well.
  • Dip a glass rod in ammonium hydroxide solution.
  • Bring the glass rod near the mouth of the test tube.
  • If white fumes appear, then the presence of an alcoholic group is confirmed.

Iodoform Test:

  • Add 1ml of the given organic compound to a clean dry test tube.
  • Add 1ml of 1% iodine solution to it.
  • Add dilute sodium hydroxide solution dropwise until the brown colour of iodine is discharged.
  • Gently heat the mixture in a water bath.
  • The formation of a yellow precipitate indicates the presence of either ethanol or acetaldehyde or methyl ketone.

Observations:

Test

Observation

Sodium Metal Test

Brisk effervescence indicates the presence of an alcoholic group.

Ester Test

A sweet smell indicates the presence of an alcoholic group.

Ceric Ammonium Nitrate Test

The appearance of a wine red colour precipitate indicates the presence of an alcoholic group.

Acetyl Chloride Test

The formation of white fumes indicates the presence of alcohol.

Iodoform Test

The formation of a yellow precipitate indicates the presence of alcohol.

Safety Precautions While Testing

When performing alcohol in the lab, it’s important to follow proper safety steps. Even though these tests are simple, they involve strong acids, reactive metals, and flammable substances, so you must be careful.

Here are some important precautions to keep in mind:

  • Wear safety gear: Always wear a lab coat, gloves, and safety goggles to protect your skin and eyes
  • Handle acids carefully: Lucas reagent contains concentrated hydrochloric acid, which can cause burns. Use it with care
  • Be cautious with Sodium: In the sodium test, metal sodium reacts quickly and releases hydrogen gas. Cut it with dry forceps and never touch it with bare hands
  • Work in a well ventilated area: Some tests produce gases or strong smells (like esters), so it’s better to perform them in a fume hood or open space
  • Keep flammable materials away: Alcohols and esters can catch fire easily. Don’t use open flames nearby
  • Dispose of chemical properly: Follow your teacher’s or lab instructions for disposing used chemicals safely

Summary table 

Test Name

What You Do

What You See

What It Means

Lucas Test

Add Lucas reagent to alcohol and shake

Cloudiness appears (time depends on type)

Tells whether alcohol is primary, secondary, or tertiary

Sodium Metal Test

Add small piece of sodium to alcohol

Effervescence (bubbles of hydrogen gas)

Confirms presence of –OH group

Esterification Test

Mix alcohol with carboxylic acid and a few drops of acid

Fruity smell (ester formed)

Confirms alcohol is present

CAN Test

Add ceric ammonium nitrate to alcohol solution

Color changes from yellow to red/orange

Alcohol is present in the sample


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FAQs

The mixture of anhydrous zinc chloride in 100ml of concentrated hydrochloric acid is called Lucas reagent.

Lucas ‘ reagent is a concentrated hydrochloric acid solution of anhydrous zinc chloride. Used to classify low molecular weight alcohols. The reaction is a substitution reaction where a hydroxyl group is replaced by the chloride.

Some functional groups are, Hydroxyl group (-OH), Amino group (-NH3), Acid group (-COOH), Aldehyde group (-CHO)

Alcohol is dried completely before carrying out sodium metal test because sodium itself reacts with water vigorously.

Alcohols are less acidic than phenols because the removal of H ion from alcohol is very difficult. Phenol can easily lose ion because the formed phenoxide ion is somewhat stabilized by resonance.

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