How can ethanol and ethanoic acid be differentiated on the basis of their physical and chemical properties?

How can ethanol and ethanoic acid be differentiated on the basis of their physical and chemical properties

NCERT Class 10 Science | Chapter: Carbon and Its Compounds | Texcellency Book Series

✅ Answer in Brief (For Quick Revision)

Ethanol (C₂H₅OH) and ethanoic acid (CH₃COOH) can be differentiated by both physical and chemical properties. Physically — they differ in smell (alcoholic vs sour vinegar), boiling point (78°C vs 118°C), freezing point (–114°C vs 16.6°C), and nature (neutral vs acidic). Chemically — ethanoic acid turns blue litmus red and fizzes with Na₂CO₃ (releasing CO₂), while ethanol does neither. These differences reflect the fundamental chemical difference between them — ethanol has a neutral –OH group while ethanoic acid has an acidic –COOH group.

🏭 The Wine and Vinegar Analogy

Ethanol and ethanoic acid are not strangers — they are chemically related. Ethanoic acid is literally made FROM ethanol by oxidation. When wine (which contains ethanol) is left open, bacteria in air oxidise the ethanol → ethanoic acid. The wine goes sour and becomes vinegar. So the difference between ethanol and ethanoic acid is the difference between fresh wine and old sour vinegar — and you can tell them apart by smell alone even before doing any chemistry.

🔵 Ethanol → smells like wine, whisky, spirit — the familiar alcoholic smell 🔵 Ethanoic acid → smells like vinegar — sharp, sour, pungent — the smell that makes your eyes water

But in chemistry, we need more than smell. We need precise physical measurements and confirmed chemical reactions. Here is the complete differentiation.

🔴 Physical Properties — Differentiation

Property 1 — Smell (Most Obvious Physical Difference): 🔵 Ethanol: Pleasant, characteristic alcoholic smell — the smell of wine, beer, spirit 🔵 Ethanoic acid: Sharp, pungent, sour smell — the smell of vinegar (which is 5–8% ethanoic acid in water) 🔵 Verdict: Easily distinguishable by smell alone ✅

Property 2 — Taste: 🔵 Ethanol: Burning, warming sensation — the taste characteristic of alcoholic beverages 🔵 Ethanoic acid: Intensely sour taste — the sour taste of vinegar 🔵 Note: In laboratory settings, tasting chemicals is NOT recommended. This is only for understanding — vinegar is the safe real-life example of ethanoic acid.

Property 3 — Boiling Point: 🔵 Ethanol: boiling point = 78.4°C 🔵 Ethanoic acid: boiling point = 117.9°C 🔵 Ethanoic acid boils at a significantly higher temperature — nearly 40°C higher — because its molecules form stronger intermolecular hydrogen bonds (two –COOH groups can hydrogen bond with each other, forming dimers) 🔵 Verdict: A clear measurable physical difference ✅

Property 4 — Freezing/Melting Point (The Glacial Acetic Acid Fact — Exam Gold): 🔵 Ethanol: freezing point = –114.1°C — remains liquid at all normal temperatures, even cold weather 🔵 Ethanoic acid: freezing point = 16.6°C — this is just BELOW room temperature 🔵 This means: on a cold winter day (when temperature drops below 16.6°C), pure ethanoic acid can solidify into a colourless ice-like solid in the laboratory 🔵 This solidified form of pure ethanoic acid is called “Glacial Acetic Acid” — because it resembles glacial ice 🔵 This is a remarkable and exam-favourite property — ethanol would NEVER solidify under normal conditions, but ethanoic acid can solidify on a cold day 🔵 Verdict: Dramatic, measurable, and memorable physical difference ✅

Property 5 — Nature (Acidic vs Neutral): 🔵 Ethanol: neutral — pH ≈ 7 — does not change litmus 🔵 Ethanoic acid: acidic — pH ≈ 2.9 to 3.5 (depending on concentration) — turns blue litmus red 🔵 Though this is detected by a chemical indicator (litmus), the underlying difference (acidic vs neutral nature) is a fundamental property of the substances themselves 🔵 Verdict: Most important and most exam-relevant physical/chemical property difference ✅

Property 6 — Density: 🔵 Ethanol: 0.789 g/mL at 20°C 🔵 Ethanoic acid: 1.049 g/mL at 20°C 🔵 Ethanoic acid is denser than ethanol — and denser than water (1.0 g/mL) 🔵 Verdict: Measurable laboratory difference ✅

🔶 Chemical Properties — Differentiation

Chemical Test 1 — Litmus Paper Test (Quickest Chemical Test):

Procedure: Dip a strip of blue litmus paper into each substance.

🔵 Ethanol + blue litmus → no colour change — ethanol is neutral (–OH group does not release H⁺ ions) 🔵 Ethanoic acid + blue litmus → turns RED — ethanoic acid is acidic (–COOH group releases H⁺ ions: CH₃COOH ⇌ CH₃COO⁻ + H⁺)

Verdict: Blue litmus test is a simple, instant differentiating test ✅

Chemical Test 2 — Sodium Carbonate / Sodium Bicarbonate Test (Most Important — NCERT Expected):

Procedure: Add a few drops of each substance to sodium carbonate (Na₂CO₃) or sodium bicarbonate (NaHCO₃) solution in separate test tubes. Observe.

🔵 Ethanol + Na₂CO₃ → No reaction. No fizzing. No gas evolved. 🔵 Ethanoic acid + Na₂CO₃ → Brisk effervescence. CO₂ gas evolved. Fizzing observed.

Chemical equation: 2CH₃COOH + Na₂CO₃ → 2CH₃COONa + H₂O + CO₂↑ (Ethanoic acid + Sodium carbonate → Sodium ethanoate + Water + Carbon dioxide)

To confirm CO₂: pass the gas through lime water → lime water turns milky: CO₂ + Ca(OH)₂ → CaCO₃↓ + H₂O

Why ethanol does not react: ethanol is neutral — it has no acidic H⁺ to donate to the carbonate ion. Na₂CO₃ is a base — it only reacts with acids, not with neutral substances.

Verdict: The most reliable and NCERT-recommended chemical differentiating test ✅

Chemical Test 3 — Reaction with NaOH (Sodium Hydroxide):

Procedure: Add NaOH solution to each substance.

🔵 Ethanol + NaOH → No reaction — ethanol is not acidic enough to react with NaOH under normal conditions 🔵 Ethanoic acid + NaOH → Neutralisation reaction — ethanoic acid reacts with NaOH (a base) to form sodium ethanoate (a salt) and water:

CH₃COOH + NaOH → CH₃COONa + H₂O (Ethanoic acid + Sodium hydroxide → Sodium ethanoate + Water)

This is a standard acid-base neutralisation. Ethanol being neutral does not undergo this reaction.

Verdict: Another clear chemical differentiating test ✅

Chemical Test 4 — Esterification Test (The Sweet Smell Test):

Procedure: To a sample of the unknown substance, add ethanol (if testing for acid) or ethanoic acid (if testing for alcohol) along with a few drops of concentrated H₂SO₄ (catalyst). Warm gently and pour into water. Smell carefully.

🔵 Ethanoic acid + ethanol + conc. H₂SO₄ + heat → sweet, fruity smell (ethyl ethanoate ester formed): CH₃COOH + C₂H₅OH ⇌ CH₃COOC₂H₅ + H₂O (Ethanoic acid + Ethanol → Ethyl ethanoate + Water)

🔵 Ethanol alone + conc. H₂SO₄ + heat → no sweet ester smell (without a carboxylic acid partner, no ester forms under these conditions)

Verdict: The esterification test confirms the presence of the carboxylic acid group in ethanoic acid ✅

Important note on sodium metal test: BOTH ethanol and ethanoic acid react with sodium metal to produce hydrogen gas. Therefore the sodium metal test CANNOT be used to differentiate them — it is not a valid distinguishing test for this pair. Do not use it in your answer.

🔷 The Root Cause — Why They Behave So Differently

All the physical and chemical differences between ethanol and ethanoic acid trace back to ONE fundamental structural difference:

🔵 Ethanol has –OH (hydroxyl group): This –OH does NOT release H⁺ in water. Ethanol is neutral. The –OH can form hydrogen bonds with water (explaining its high miscibility with water) but it does not donate protons to bases or indicators.

🔵 Ethanoic acid has –COOH (carboxyl group): The –COOH IS acidic — it releases H⁺ in water: CH₃COOH ⇌ CH₃COO⁻ + H⁺ This H⁺ is what turns litmus red, reacts with Na₂CO₃ to give CO₂, neutralises NaOH, and makes ethanoic acid sour to taste.

The –COOH group is acidic because the C=O part of it pulls electron density away from the –OH part, making it easier for the –OH to release its H⁺ as a proton. In plain ethanol (–OH only), there is no C=O pulling electrons away — so the H is not released as H⁺. This is why alcohols are neutral and carboxylic acids are acidic.

🔴 Real-Life Connections

🔵 Ethanol in daily life: wine, beer, whisky, brandy (alcoholic beverages) — all contain ethanol as the active ingredient. Also used as a solvent, antiseptic (sanitisers), and fuel (biofuel). 🔵 Ethanoic acid in daily life: vinegar (5–8% ethanoic acid in water) — used in cooking, pickling, preserving food. Also used industrially to make plastics (PET — polyethylene terephthalate), synthetic fibres, and pharmaceuticals (aspirin is acetylsalicylic acid — made using ethanoic acid/acetic anhydride). 🔵 Glacial acetic acid in labs: pure ethanoic acid used as a solvent and reagent in chemical synthesis. Its freezing at 16.6°C is a well-known laboratory phenomenon. 🔵 The oxidation connection: ethanol → ethanoic acid is the same reaction that sours wine into vinegar. KMnO₄ or K₂Cr₂O₇ in the lab does in minutes what bacteria do in days.

📊 Master Comparison Table — Ethanol vs Ethanoic Acid

Name: Ethanol vs Ethanoic Acid Formula: C₂H₅OH vs CH₃COOH Functional group: –OH (hydroxyl) vs –COOH (carboxyl) Nature: Neutral (pH ≈ 7) vs Acidic (pH ≈ 2.9–3.5) Smell: Alcoholic (wine/spirit) vs Sharp, sour (vinegar) Boiling point: 78.4°C vs 117.9°C Freezing point: –114.1°C vs 16.6°C (glacial acetic acid) Density: 0.789 g/mL vs 1.049 g/mL Blue litmus test: No change vs Turns RED Na₂CO₃ test: No reaction vs Brisk fizzing (CO₂ released) NaOH reaction: No reaction vs Neutralisation (forms CH₃COONa + H₂O) Esterification: Forms ester WITH acid vs Forms ester WITH alcohol Na metal test: Reacts (H₂ gas) vs Also reacts (H₂ gas) — NOT a distinguishing test Real-life example: Wine, sanitiser, biofuel vs Vinegar, food preservative Made from: Fermentation of sugars vs Oxidation of ethanol

🎵 Rhyme to Remember

“Ethanol smells like wine so fine, Neutral nature — it’s doing fine,* Blue litmus? No change — it just walks past,* Na₂CO₃? No fizz — no reaction, no blast!* But ethanoic acid — sharp like a knife,* The sour smell of vinegar — the taste of strife!* Blue litmus turns RED — it’s acidic, you see,* Na₂CO₃ fizzes — CO₂ breaks free!* Boils at 118, freezes at 16.6 degrees,* Glacial acetic acid — solid on cold days with ease!”*

🧩 Mnemonics

🔵 “ETHANOL = Easy going, Neutral, No fizz with Na₂CO₃” — the three key facts about ethanol in one phrase. 🔵 “ETHANOIC = Energetically Acidic, CO₂ with Na₂CO₃, Turns litmus Red, Neutralises NaOH, Esterifies, Glacial at 16.6°C” — every key property in the name. 🔵 “–OH = Only Hangs on, never lets go of H⁺ (neutral). –COOH = Constantly Outputs OH-stripped H⁺ (acidic).” 🔵 “Glacial acetic acid = ethanoic acid freezes at 16.6°C = looks like ICE in cold lab.” 🔵 “Na₂CO₃ test: ACID fizzes, ALCOHOL misses” — from our earlier post — applies perfectly here too.

✅ Exam-Ready Answer (Write This in Board Exam)

How can ethanol and ethanoic acid be differentiated on the basis of their physical and chemical properties?

A. Physical Properties:

1. Smell: Ethanol has a characteristic alcoholic smell (like wine or spirit). Ethanoic acid has a sharp, sour, pungent smell (like vinegar).

2. Boiling Point: Ethanol boils at 78.4°C. Ethanoic acid boils at a higher temperature — 117.9°C — due to stronger intermolecular hydrogen bonding.

3. Freezing Point: Ethanol freezes at –114.1°C (never solidifies under normal conditions). Ethanoic acid freezes at 16.6°C — pure ethanoic acid can solidify into an ice-like solid on cold days. This solid form is called Glacial Acetic Acid.

4. Nature: Ethanol is neutral (pH ≈ 7). Ethanoic acid is acidic (pH ≈ 2.9–3.5).

B. Chemical Properties:

1. Litmus Test: Ethanol does not change the colour of blue litmus paper (neutral). Ethanoic acid turns blue litmus red (acidic).

2. Sodium Carbonate Test (Na₂CO₃ Test): 🔵 Ethanol + Na₂CO₃ → No reaction. No fizzing. 🔵 Ethanoic acid + Na₂CO₃ → Brisk effervescence. CO₂ gas evolved, which turns lime water milky. 2CH₃COOH + Na₂CO₃ → 2CH₃COONa + H₂O + CO₂↑

3. Reaction with NaOH: 🔵 Ethanol + NaOH → No reaction. 🔵 Ethanoic acid + NaOH → Neutralisation: CH₃COOH + NaOH → CH₃COONa + H₂O

4. Esterification Test: 🔵 When ethanoic acid is mixed with ethanol in the presence of conc. H₂SO₄ and heated, a sweet-smelling ester (ethyl ethanoate) is formed: CH₃COOH + C₂H₅OH ⇌ CH₃COOC₂H₅ + H₂O 🔵 Ethanol alone does not produce this sweet smell.

📌 Key Points Checklist

✅ Ethanol = C₂H₅OH, –OH group, neutral, pH ≈ 7, alcoholic smell, boils at 78.4°C, freezes at –114.1°C ✅ Ethanoic acid = CH₃COOH, –COOH group, acidic, pH ≈ 2.9–3.5, vinegar smell, boils at 117.9°C, freezes at 16.6°C ✅ Glacial acetic acid = pure ethanoic acid solidified at/below 16.6°C — looks like ice ✅ Blue litmus: ethanol = no change | ethanoic acid = turns RED ✅ Na₂CO₃ test: ethanol = no reaction | ethanoic acid = CO₂ fizzing (2CH₃COOH + Na₂CO₃ → 2CH₃COONa + H₂O + CO₂↑) ✅ NaOH reaction: ethanol = no reaction | ethanoic acid = neutralisation (CH₃COOH + NaOH → CH₃COONa + H₂O) ✅ Esterification: ethanoic acid + ethanol + conc. H₂SO₄ + heat → sweet-smelling ethyl ethanoate ✅ Sodium metal test: BOTH react with Na giving H₂ — NOT a valid distinguishing test for this pair ✅ Root cause of all differences: –OH (neutral, no H⁺ release) vs –COOH (acidic, releases H⁺) ✅ Real life: ethanol = wine/sanitiser/biofuel | ethanoic acid = vinegar/food preservative/aspirin manufacturing

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