Over 100 Q&A on Tests for Functional Groups in Organic Chemistry (JEE/NEET Focus)
Part 1: Alcohols and Phenols
| Q. No. | Functional Group | Test Name/Reagent | Observation/Key Result |
| 1 | -OH (Alcohol) | Sodium Metal Test (Na) | Effervescence of H2 gas (2ROH+2Na→2RO−Na++H2). |
| 2 | -OH (Alcohol) | Esterification Test (RCOOH/H+) | Fruity smell of the ester. |
| 3 | 1∘,2∘,3∘ Alcohols | Lucas Test (ZnCl2/HCl) | 3∘ shows immediate turbidity; 2∘ after 5 min; 1∘ no turbidity at RT. |
| 4 | CH3CH(OH)− | Iodoform Test (I2/NaOH) | Yellow precipitate of CHI3. |
| 5 | Phenol (Ar−OH) | Neutral FeCl3 Test | Violet, green, or blue color (complex formation). |
| 6 | Phenol (Ar−OH) | Bromine Water Test (Br2(aq)) | White precipitate of 2,4,6-Tribromophenol. |
| 7 | Phenol (Ar−OH) | Litmus Test | Turns blue litmus red (weakly acidic). |
| 8 | 1∘ vs 2∘ Alcohol | Cu at 573 K | 1∘→Aldehyde; 2∘→Ketone; 3∘→Alkene (Dehydration). |
Part 2: Aldehydes and Ketones (C=O) Group
| Q. No. | Functional Group | Test Name/Reagent | Observation/Key Result |
| 9 | C=O (Aldehyde/Ketone) | 2,4-DNP Test | Yellow, orange, or red precipitate (Schiff's base). |
| 10 | Aldehyde (RCHO) | Tollen's Test (Ag(NH3)2+) | Silver Mirror on the inner wall of the test tube. |
| 11 | Aldehyde (RCHO) | Fehling's Test (Cu2+ complex) | Red-brown precipitate of Cu2O. |
| 12 | Aldehyde (RCHO) | Schiff's Test | Restores the pink/magenta color of Schiff's reagent. |
| 13 | Ketone (RCOR′) | Tollen's/Fehling's | No reaction (except α-hydroxy ketones). |
| 14 | CH3CO− (Methyl Ketone) | Iodoform Test (I2/NaOH) | Yellow precipitate of CHI3. |
| 15 | Aromatic Aldehyde (ArCHO) | Tollen's/Fehling's | Tollen's OK (Silver mirror); Fehling's Fail (Aromatic aldehyde usually resists Fehling’s). |
| 16 | Ketones that don't respond to Iodoform | Tollen's/Fehling's | Both tests are negative. |
Part 3: Carboxylic Acids and Esters
| Q. No. | Functional Group | Test Name/Reagent | Observation/Key Result |
| 17 | -COOH (Carboxylic Acid) | Sodium Bicarbonate Test (NaHCO3) | Brisk effervescence of CO2 gas. |
| 18 | -COOH (Carboxylic Acid) | Blue Litmus Test | Turns blue litmus red (stronger acid than phenol). |
| 19 | -COOH (Carboxylic Acid) | Esterification Test (R′OH/H+) | Fruity smell of the ester formed. |
| 20 | -COOH (Carboxylic Acid) | Neutral FeCl3 Test (for Aromatic COOH) | Buff-colored precipitate of ferric carboxylate. |
| 21 | Ester (RCOOR′) | Hydroxamic Acid Test | Deep red color with FeCl3 after hydrolysis (formation of RCONHOH). |
| 22 | Formic Acid (HCOOH) | Tollen's Test | Silver Mirror (HCOOH is easily oxidized like an aldehyde). |
Part 4: Amines and Nitrogen Compounds
| Q. No. | Functional Group | Test Name/Reagent | Observation/Key Result |
| 23 | NH2 (1∘ Amine) | Carbylamine Test (CHCl3/KOH) | Foul/offensive smell of Isocyanide (R−NC). |
| 24 | 1∘,2∘,3∘ Amines | Hinsberg's Test (C6H5SO2Cl) | 1∘→Soluble in KOH; 2∘→Insoluble; 3∘→No reaction. |
| 25 | NH2 (Amine) | Litmus Test | Turns red litmus blue (basic nature). |
| 26 | Aromatic 1∘ Amine (Aniline) | Azo Dye Test (Diazotization + Coupling with Phenol) | Bright orange/yellow dye (p-hydroxyazobenzene). |
| 27 | Nitro Compound (RNO2) | Reduction followed by FeCl3 | RNO2→RNH2→Azo Dye or Carbylamine. |
| 28 | Amide (RCONH2) | Alkaline Hydrolysis (NaOH/heat) | NH3 gas evolved (detected by Nessler's reagent or red litmus). |
Part 5: Unsaturated Hydrocarbons and Halides
| Q. No. | Functional Group | Test Name/Reagent | Observation/Key Result |
| 29 | Alkene (C=C) | Bromine Water Test (Br2/CCl4) | Decolorizes the reddish-brown color (Addition). |
| 30 | Alkene (C=C) | Baeyer's Test (Cold Dil. KMnO4) | Decolorizes the pink/purple color and forms a brown MnO2 ppt. |
| 31 | Terminal Alkyne (R−C≡CH) | Ammoniacal AgNO3 (Tollen’s) | White precipitate of silver acetylide (R−C≡C−Ag). |
| 32 | Terminal Alkyne (R−C≡CH) | Ammoniacal Cu2Cl2 | Red precipitate of copper acetylide (R−C≡C−Cu). |
| 33 | Alkyl Halide (R−X) | AgNO3 Test (after hydrolysis/boiling with KOH) | Precipitate of AgX (AgCl white, AgBr pale yellow, AgI yellow). |
| 34 | Aryl Halide (Ar−X) | AgNO3 Test (direct) | No precipitate (C−X bond is strong/no ionization). |
Part 6: Lassiagne's Test (Detection of Elements)
| Q. No. | Element | Test Principle/Reagent | Observation/Key Result |
| 35 | Nitrogen (N) | Prussian Blue Test (FeSO4+FeCl3) | Prussian blue/deep green color or ppt (Fe4[Fe(CN)6]3). |
| 36 | Sulphur (S) | Sodium Nitroprusside Test (Na2[Fe(CN)5NO]) | Deep violet/purple color. |
| 37 | Halogens (X) | AgNO3 Test (in Lassaigne's filtrate) | White/yellow/pale yellow precipitate (AgX). |
| 38 | Phosphorus (P) | Ammonium Molybdate Test | Canary yellow precipitate (Phosphomolybdate). |
| 39 | What is the purpose of preparing Lassaigne's Extract? | To convert elements (N, S, X) from covalent to ionic form for aqueous testing. | |
| 40 | What is used to make Lassaigne's Extract? | Sodium metal (fused with the organic compound). |
Part 7: Distinguishing Tests (JEE/NEET Specific)
| Q. No. | Compounds to Distinguish | Recommended Test | Key Difference |
| 41 | Methanol vs Ethanol | Iodoform Test (I2/NaOH) | Ethanol gives yellow ppt; Methanol gives none. |
| 42 | Propanal (Aldehyde) vs Propanone (Ketone) | Tollen's Test | Propanal gives Silver Mirror; Propanone gives none. |
| 43 | Phenol vs Ethanol | Neutral FeCl3 Test | Phenol gives violet color; Ethanol gives none. |
| 44 | But-1-yne (Terminal) vs But-2-yne (Non-terminal) | Ammoniacal AgNO3 Test | But-1-yne gives white ppt; But-2-yne gives none. |
| 45 | Carboxylic Acid vs Phenol | NaHCO3 Test | Carboxylic Acid gives CO2 effervescence; Phenol gives none. |
| 46 | Aniline (1∘) vs N,N-Dimethylaniline (3∘) | Hinsberg's Test | Aniline gives a KOH-soluble product; N,N-dimethylaniline is unreactive. |
| 47 | Chloroform (CHCl3) vs Carbon Tetrachloride (CCl4) | Carbylamine Test | Chloroform gives foul smell (when 1∘ amine is added); CCl4 gives none. |
| 48 | Alkyl Chloride (RCl) vs Aryl Chloride (ArCl) | Aqueous AgNO3 Test | RCl gives immediate AgCl ppt; ArCl gives none. |
| 49 | Glucose (Aldehyde) vs Fructose (Ketone) | Seliwanoff's Test | Fructose (ketose) reacts faster (Resorcinol/HCl). |
| 50 | Sucrose vs Glucose | Fehling's Test | Glucose (reducing) gives red ppt; Sucrose (non-reducing) gives none. |
Part 8: Further Concepts and Applications
| Q. No. | Concept/Application | Detail |
| 51 | Why does the Iodoform Test require the CH3CO− group? | This group is easily halogenated and cleaved by the base (NaOH) to yield CHI3. |
| 52 | Why must Tollen’s Reagent be freshly prepared? | The complex (Ag(NH3)2OH) is unstable and decomposes upon standing, forming explosive Ag2O. |
| 53 | What is the active ingredient in Tollen's Reagent? | Diamminesilver(I) hydroxide (Ag(NH3)2OH). |
| 54 | What is the active species in Fehling's Solution? | Alkaline Cu2+ ion complexed with tartrate ions. |
| 55 | Which amines (1∘,2∘,3∘) form a sulphonamide precipitate in Hinsberg's Test? | 1∘ and 2∘ amines. |
| 56 | What is the role of NaOH in the Carbylamine Test? | It acts as a base to generate the reactive intermediate, Dichlorocarbene (CCl2). |
| 57 | Why does Formic Acid give Tollen's Test? | It contains the H−C=O group, which is easily oxidized to CO2. |
| 58 | What is the final product of the reaction between Acetone and 2,4-DNP? | Acetone 2,4-dinitrophenylhydrazone. |
| 59 | How do you prepare Bromine Water in the lab? | By dissolving Br2 in water. |
| 60 | What is the structural feature confirmed by a positive Baeyer's Test? | Presence of an unsaturation (C=C or C≡C). |
| 61 | What is the common name for the gas evolved in the NaHCO3 test? | Carbon dioxide (CO2). |
| 62 | What is the color of 2,4-DNP reagent itself? | Orange-yellow. |
| 63 | Why is Ethanol added to the AgNO3 solution when testing R−X? | To increase the solubility of the alkyl halide. |
| 64 | What must be done before testing a salt for a halogen by AgNO3 in the lab? | Boil with HNO3 to decompose CN− and S2− ions, which interfere. |
| 65 | What is the name of the test used to distinguish Aldose (Glucose) from Ketose (Fructose) rapidly? | Seliwanoff's Test. |
| 66 | What is the characteristic observation of a positive Molisch’s Test (for Carbohydrates)? | Purple or violet ring at the junction of the two liquids. |
| 67 | What is the role of concentrated H2SO4 in the Molisch’s Test? | It dehydrates the sugar to form furfural derivatives. |
| 68 | What is the general rule for using d-Glucose in the lab? | Always use D-Glucose (naturally occurring D-form). |
| 69 | What is the final product in the Ring Test (Nitrate) responsible for the color? | Nitroso ferrous sulphate ([Fe(H2O)5NO]SO4). |
| 70 | What is the observation when S2− is present in Lassaigne’s Extract? | Violet color with Sodium Nitroprusside. |
| 71 | What test confirms the presence of Alcohol (R−OH) over Phenol (Ar−OH)? | Lucas Test (reactivity difference). |
| 72 | Why is Acetone used as the solvent for the Finkelstein Reaction (Halide exchange)? | To precipitate the less soluble NaCl or NaBr, driving the equilibrium forward. |
| 73 | What is the color change in the Chromyl Chloride Test (Cl− detection)? | Red-brown vapors (CrO2Cl2) turning to yellow solution (Na2CrO4). |
| 74 | What is the term for the yellow precipitate formed in the Iodoform Test? | Triiodomethane (CHI3). |
| 75 | Why do Ketones generally fail the Tollen’s Test? | The C−C bond is strong and requires harsh oxidation conditions. |
| 76 | What is the key functional group necessary for a compound to be a Carbohydrate (chemically)? | Polyhydroxy (many OH groups). |
| 77 | What is the observation when Ethane-1,2-diol is added to NaHCO3? | No reaction (It's not acidic enough). |
| 78 | How do you confirm Fe3+ in qualitative analysis? | K4[Fe(CN)6] giving a Prussian Blue ppt. |
| 79 | How do you confirm S2− in qualitative analysis? | Lead Acetate Paper turning Black (PbS). |
| 80 | What is the confirmatory test for Nitrite (NO2−)? | Starch-Iodide Test (Blue color formation). |
| 81 | What is the difference in the Bromination of Phenol in CS2 vs H2O? | CS2→Monosubstitution; H2O→Trisubstitution (2,4,6-Tribromophenol). |
| 82 | What is the reagent used in the Haloform reaction? | X2 (halogen) and NaOH (or NaOX). |
| 83 | What is the precipitate in the DNPH test? | Hydrazone (Schiff’s base). |
| 84 | Which amines (1∘,2∘,3∘) react with HNO2 to give an alcohol and N2 gas? | Primary Aliphatic Amines (RNH2). |
| 85 | What is the product of the reaction between a primary amine and Nitrous Acid (HNO2)? | Alcohol (R−OH). |
| 86 | What is the test used to distinguish between a primary and secondary halide using AgNO3? | No, AgNO3 tests only for the presence of X− ion (reactivity difference is better seen in SN1/SN2 conditions). |
| 87 | Why is the Sulphur test usually negative in Lassaigne’s if Nitrogen is also present? | They combine to form NaCNS (Sodium thiocyanate), which needs a separate test. |
| 88 | What color does Fehling’s Solution A and B form when mixed? | Blue color. |
| 89 | What is the Acid-Base indicator used in the Carbylamine reaction? | None, it is a functional group test based on smell. |
| 90 | What is the term for the characteristic smell of the product of the Esterification reaction? | Fruity smell. |
| 91 | What is the difference between Methyl Ketone and Ethyl Ketone? | Methyl Ketones have the CH3CO− group and give the Iodoform Test. |
| 92 | What is the simplest alcohol that gives the Iodoform Test? | Ethanol (CH3CH2OH). |
| 93 | What is the test used to confirm Phenol over Carboxylic Acid after the NaHCO3 test? | Neutral FeCl3 Test. |
| 94 | Which reagent is used to confirm the presence of reducing sugar in a solution? | Fehling's Solution or Benedict's Solution. |
| 95 | How is the H2 gas evolved in the Sodium Metal Test confirmed? | It burns with a pop sound. |
| 96 | What is the formula of the Nessler’s Reagent? | Alkaline solution of K2[HgI4] (Potassium Tetraiodomercurate(II)). |
| 97 | What is the observation in the Nessler’s Test for Ammonia? | Brown/reddish-brown precipitate or coloration. |
| 98 | What is the role of concentrated HNO3 in the Halogen test in Lassaigne’s? | It removes the unreacted CN− and S2− before adding AgNO3. |
| 99 | How can you distinguish between Acetic Acid and Formic Acid? | Tollen’s Test (Formic acid gives silver mirror, Acetic acid does not). |
| 100 | Why is the Bromine Water Test not sufficient to prove unsaturation in all cases? | Phenol also decolorizes Br2 water (Substitution vs Addition). |
| 101 | What color does Acidified KMnO4 change to when an alkene is present? | Pink to colorless (Baeyer’s Test). |
| 102 | What is the reagent used in the Diazotization reaction? | NaNO2/HCl at 0−5∘C. |
| 103 | What is the test that produces a precipitate that is soluble in excess NaOH? | Aluminium Hydroxide (Al3+ confirmatory test). |
| 104 | Which amines (1∘,2∘,3∘) react with Benzoyl Chloride? | 1∘ and 2∘ amines. |
| 105 | What is the term for the precipitate formed when DNPH reacts with Ketones? | Ketone 2,4-dinitrophenylhydrazone. |
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