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Ethanol and Ethanoic Acid: Properties and Reactions for CBSE Class 10

Master the properties and reactions of Ethanol and Ethanoic Acid for CBSE Class 10 Science. Learn esterification, saponification, reactions with sodium, dehydration, glacial acetic acid, and the chemical test to distinguish alcohol from acid.

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Updated 14 September 2026

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Among the vast array of commercially manufactured carbon compounds, two compounds hold immense industrial, domestic, and laboratory significance: Ethanol (the primary alcohol) and Ethanoic Acid (commonly known as acetic acid). Ethanol is a versatile industrial solvent and medicine vehicle, while ethanoic acid is the active ingredient in kitchen vinegar and synthetic fabrics.

In CBSE Class 10 Science, Chapter 4 (Carbon and its Compounds) dedicates an entire section to their physical properties, physiological impacts, and four classic chemical reactions: Esterification, Saponification, Dehydration, and Carbonate Effervescence.


What You Will Learn

  • Chemical formula, physical properties, and commercial uses of Ethanol
  • Reactions of ethanol: reaction with sodium metal and dehydration with concentrated H2SO4\text{H}_2\text{SO}_4
  • Harmful biological effects of alcohol and denatured alcohol
  • Chemical formula, physical properties, and Glacial Acetic Acid
  • Reactions of ethanoic acid: Esterification and Saponification
  • Reaction with carbonates and bicarbonates (the definitive diagnostic test)
  • Step-by-step chemical test to distinguish between ethanol and ethanoic acid

1. Ethanol (extCH3extCH2extOH ext{CH}_3 ext{CH}_2 ext{OH})

Physical Properties:

  • Formula: C2H5OH\text{C}_2\text{H}_5\text{OH} or CH3−CH2−OH\text{CH}_3-\text{CH}_2-\text{OH}
  • Appearance: Colourless liquid with a pleasant alcoholic odour and a burning taste.
  • Boiling Point: 78∘C78^\circ\text{C} (351 K351\text{ K}).
  • Solubility: Highly soluble in water in all proportions due to hydrogen bonding.
  • Nature: Neutral to litmus (does not change the colour of blue or red litmus paper).

Chemical Reactions of Ethanol:

1. Reaction with Sodium Metal (Hydrogen Evolution)

When a tiny piece of sodium metal is dropped into absolute ethanol, effervescence occurs as hydrogen gas is released: 2CH3CH2OH+2Na⟶2CH3CH2ONa [Sodium Ethoxide]+H2(g)↑2\text{CH}_3\text{CH}_2\text{OH} + 2\text{Na} \longrightarrow 2\text{CH}_3\text{CH}_2\text{ONa} \text{ [Sodium Ethoxide]} + \text{H}_2(g) \uparrow The evolved hydrogen gas burns with a pop sound. This reaction serves as a standard laboratory test for the alcohol group.

2. Dehydration Reaction (Formation of Ethene)

When ethanol is heated with excess concentrated sulphuric acid at strictly 443 K443\text{ K} (170∘C170^\circ\text{C}), water is eliminated to produce unsaturated ethene gas:

CH3CH2OH→443 KConc. H2SO4CH2=CH2 [Ethene]+H2O\text{CH}_3\text{CH}_2\text{OH} \xrightarrow[443\text{ K}]{\text{Conc. } \text{H}_2\text{SO}_4} \text{CH}_2=\text{CH}_2 \text{ [Ethene]} + \text{H}_2\text{O}

Important: <u>In this reaction, concentrated sulphuric acid acts as a powerful DEHYDRATING AGENT—a substance that removes water molecules from a compound.</u>


Biological Effects and Denatured Alcohol:

  • Ingestion of ethanol depresses the central nervous system, impairs judgment, slows reflexes, and causes metabolic damage to the liver.
  • Methanol Poisoning: Ingestion of even small quantities of methanol (CH3OH\text{CH}_3\text{OH}) is fatal. Methanol is oxidized to methanal (formaldehyde) in the liver, which coagulates cellular protoplasm and attacks the optic nerve, causing permanent blindness and death.
  • What is Denatured Alcohol? To prevent the misuse of cheap industrial alcohol for drinking, it is made poisonous by adding small amounts of methanol, pyridine, and blue copper sulphate dye. This foul-tasting, poisonous mixture is called denatured alcohol.

2. Ethanoic Acid (extCH3extCOOH ext{CH}_3 ext{COOH})

Physical Properties:

  • Formula: CH3COOH\text{CH}_3\text{COOH} (commonly called acetic acid).
  • Appearance: Colourless liquid with a sharp, pungent vinegar smell and sour taste.
  • Vinegar: A 5%−8%5\% - 8\% solution of acetic acid in water is called vinegar, used widely as a food preservative in pickles.
  • Glacial Acetic Acid: The melting point of pure ethanoic acid is 290 K290\text{ K} (17∘C17^\circ\text{C}). In cold climates or during winter, pure ethanoic acid freezes into an ice-like crystalline solid, earning it the name glacial acetic acid.

Chemical Reactions of Ethanoic Acid:

1. Esterification Reaction (Formation of Sweet-Smelling Esters)

When ethanoic acid is heated with absolute ethanol in the presence of a few drops of concentrated sulphuric acid (catalyst), a fruity, sweet-smelling compound called an ester (ethyl ethanoate) is formed:

CH3COOH [Ethanoic acid]+CH3CH2OH [Ethanol]→Acid CatalystCH3COOCH2CH3 [Ethyl Ethanoate / Ester]+H2O\text{CH}_3\text{COOH} \text{ [Ethanoic acid]} + \text{CH}_3\text{CH}_2\text{OH} \text{ [Ethanol]} \xrightarrow{\quad \text{Acid Catalyst} \quad} \text{CH}_3\text{COOCH}_2\text{CH}_3 \text{ [Ethyl Ethanoate / Ester]} + \text{H}_2\text{O}

  • Esters are sweet-smelling substances used in making perfumes and artificial flavouring agents (e.g., in candies and ice creams).

2. Saponification Reaction (Alkaline Hydrolysis of Esters)

When an ester is treated with an alkali like sodium hydroxide, it hydrolyzes back into alcohol and the sodium salt of the carboxylic acid: CH3COOCH2CH3+NaOH⟶CH3COONa [Sodium Ethanoate]+CH3CH2OH [Ethanol]\text{CH}_3\text{COOCH}_2\text{CH}_3 + \text{NaOH} \longrightarrow \text{CH}_3\text{COONa} \text{ [Sodium Ethanoate]} + \text{CH}_3\text{CH}_2\text{OH} \text{ [Ethanol]} This reaction is called saponification because it is the exact chemical reaction used in the industrial manufacture of soaps from natural fats!

3. Reaction with Carbonates and Bicarbonates (The Diagnostic Test)

Ethanoic acid reacts with sodium carbonate and sodium hydrogen carbonate to produce brisk effervescence of carbon dioxide gas: CH3COOH+NaHCO3⟶CH3COONa+H2O+CO2(g)↑\text{CH}_3\text{COOH} + \text{NaHCO}_3 \longrightarrow \text{CH}_3\text{COONa} + \text{H}_2\text{O} + \text{CO}_2(g) \uparrow 2CH3COOH+Na2CO3⟶2CH3COONa+H2O+CO2(g)↑2\text{CH}_3\text{COOH} + \text{Na}_2\text{CO}_3 \longrightarrow 2\text{CH}_3\text{COONa} + \text{H}_2\text{O} + \text{CO}_2(g) \uparrow The liberated CO2\text{CO}_2 gas turns lime water milky.


3. How to Distinguish Chemically Between Ethanol and Ethanoic Acid

In board exams, you will frequently encounter the question: "Give a chemical test to distinguish between ethanol and ethanoic acid."

Diagnostic TestEthanol (CH3CH2OH\text{CH}_3\text{CH}_2\text{OH})Ethanoic Acid (CH3COOH\text{CH}_3\text{COOH})
1. Sodium Hydrogen Carbonate Test (Recommended!)No reaction; no gas or effervescence observed.Brisk effervescence; colourless CO2\text{CO}_2 gas evolves that turns lime water milky.
2. Litmus Paper TestNeutral; no colour change on blue or red litmus.Acidic; turns blue litmus paper red.

4. Summary and Examination Tips

CompoundKey ReactionEquation / Observation
EthanolDehydration at 443 K443\text{ K}CH3CH2OH→Conc. H2SO4CH2=CH2+H2O\text{CH}_3\text{CH}_2\text{OH} \xrightarrow{\text{Conc. }\text{H}_2\text{SO}_4} \text{CH}_2=\text{CH}_2 + \text{H}_2\text{O}
EthanolReaction with SodiumLiberates H2\text{H}_2 gas (burns with pop sound)
Ethanoic AcidEsterificationForms fruity, sweet-smelling ethyl ethanoate ester
Ethanoic AcidCarbonate ReactionBrisk effervescence of CO2\text{CO}_2 gas (turns lime water milky)

Exam Tip: Always state the Sodium Bicarbonate test when asked to distinguish between an alcohol and a carboxylic acid. It gives a clear, unmistakable visual indicator (brisk bubbling) that earns full marks immediately!

Common Mistake: Confusing esterification with saponification. Esterification is Acid + Alcohol →\to Ester + Water. Saponification is Ester + Base →\to Soap (Salt) + Alcohol!

Concept Check

HARD

If α\alpha and β\beta are the zeros of the quadratic polynomial f(x)=x2−5x+kf(x) = x^2 - 5x + k such that α−β=1\alpha - \beta = 1, find the value of kk.

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