Aldehydes, Ketones, and Carboxylic Acids (Class 12 NCERT) Revision Notes
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short question-and-answer pairs covering the essential concepts, preparation, properties, and reactions from the NCERT Class 12 Chemistry Chapter:
Short Q&A for Aldehydes, Ketones, and Carboxylic Acids (Class 12 NCERT)
Part 1: Structure and Nomenclature
| Q. No. | Question | Answer |
| 1 | What is the common functional group present in aldehydes and ketones? | The Carbonyl Group (C=O). |
| 2 | What is the hybridization of the carbonyl carbon? | sp2 hybridization. |
| 3 | What is the geometry around the carbonyl carbon? | Trigonal Planar (bond angle ≈120∘). |
| 4 | Why is the carbonyl group polar? | Oxygen is more electronegative than carbon, resulting in a partial positive charge on C. |
| 5 | Define an Aldehyde. | A carbonyl group bonded to at least one hydrogen atom (RCHO). |
| 6 | Define a Ketone. | A carbonyl group bonded to two alkyl or aryl groups (RCOR′). |
| 7 | What is the functional group in Carboxylic Acids? | The Carboxyl Group (-COOH). |
| 8 | Write the IUPAC name for CH3CHO. | Ethanal (Acetaldehyde). |
| 9 | Write the IUPAC name for CH3COCH3. | Propanone (Acetone). |
| 10 | Write the IUPAC name for C6H5CHO. | Benzaldehyde. |
| 11 | What is the common name for Methanoic Acid? | Formic Acid. |
| 12 | What is the common name for Ethanoic Acid? | Acetic Acid. |
Part 2: Preparation of Aldehydes and Ketones
| Q. No. | Question | Answer |
| 13 | What is the product of the oxidation of a Primary (1∘) alcohol using PCC? | Aldehyde (RCHO). |
| 14 | What is the product of the oxidation of a Secondary (2∘) alcohol? | Ketone (RCOR′). |
| 15 | What is the use of the reagent PCC (Pyridinium Chlorochromate)? | Selective oxidation of 1∘ alcohols to aldehydes (prevents over-oxidation). |
| 16 | What is the main product of the ozonolysis of But-2-ene followed by workup with Zn/H2O? | Ethanal (CH3CHO). |
| 17 | What is the process of converting an alkyne to a carbonyl compound using H2SO4 and HgSO4? | Hydration of Alkynes. |
| 18 | What is the specific reagent used in Stephen Reaction? | SnCl2 and HCl followed by hydrolysis, used to convert nitriles to aldehydes. |
| 19 | What is the major product when Toluene is oxidized with CrO2Cl2 (Chromyl Chloride)? | Benzaldehyde (Etard Reaction). |
| 20 | What is the process of converting an alkyl benzene to an aldehyde using CrO3 in Acetic Anhydride? | Etard Reaction (alternative method). |
| 21 | Name the reaction used to prepare aromatic aldehydes by treating benzene with CO/HCl in the presence of AlCl3. | Gattermann-Koch Reaction. |
| 22 | How are ketones prepared from Acyl Chlorides? | Reaction with Dialkylcadmium (R2Cd). |
| 23 | How is Benzaldehyde prepared by the reduction of Benzoyl Chloride over a poisoned catalyst? | Rosenmund Reduction (H2/Pd−BaSO4). |
| 24 | What is the function of the BaSO4 in Rosenmund Reduction? | It acts as a catalytic poison to prevent the over-reduction of the aldehyde to an alcohol. |
Part 3: Chemical Reactions of Aldehydes and Ketones
| Q. No. | Question | Answer |
| 25 | What is the characteristic reaction type of the carbonyl group? | Nucleophilic Addition Reactions. |
| 26 | Rank the reactivity of aldehydes and ketones toward nucleophilic addition. | Aldehydes > Ketones (Aldehydes are less sterically hindered and more electrophilic). |
| 27 | What is the product when Acetone reacts with HCN? | Acetone Cyanohydrin (a hydroxynitrile). |
| 28 | What is the product when an aldehyde reacts with a Grignard Reagent followed by hydrolysis? | Alcohol (1∘,2∘, or 3∘ depending on the starting material). |
| 29 | What is the product when an aldehyde reacts with R-OH in the presence of H+? | Acetal (followed by hemiacetal). |
| 30 | What is the product when a ketone reacts with Ethylene Glycol? | Ethylene Glycol Ketal (used as a protecting group). |
| 31 | Name the reaction where the carbonyl group is reduced to a CH2 group using Zn-Hg/conc. HCl. | Clemmensen Reduction. |
| 32 | Name the reaction where the carbonyl group is reduced to a CH2 group using Hydrazine(NH2NH2) and KOH/Ethylene Glycol. | Wolff-Kishner Reduction. |
| 33 | What is the functional group formed when a carbonyl compound reacts with Ammonia derivatives (Z-NH2)? | Imine (C=N−Z). |
| 34 | Name the reagent used to test for the presence of an aldehyde functional group. | Tollen's Reagent or Fehling's Solution. |
| 35 | What is the observation when an aldehyde reacts with Tollen's Reagent? | Formation of a Silver Mirror (Ag). |
| 36 | What is the observation when an aldehyde reacts with Fehling's Solution? | Formation of a Red-brown precipitate (Cu2O). |
| 37 | Why do ketones generally not give Tollen's and Fehling's tests? | Ketones are not easily oxidized; the tests require oxidation to a carboxylic acid. |
| 38 | What is the product when an aldehyde/ketone containing the CH3CO− group is treated with I2/NaOH? | Iodoform (CHI3, yellow precipitate) (Iodoform Test). |
Part 4: Acidity and Reactions of Carboxylic Acids
| Q. No. | Question | Answer |
| 39 | Why are Carboxylic Acids more acidic than Phenols and Alcohols? | The Carboxylate Anion (RCOO−) is stabilized by two equivalent resonance structures. |
| 40 | How does the stability of the Carboxylate Anion affect acidity? | Greater stability means stronger acid. |
| 41 | How does an Electron-Withdrawing Group (EWG) affect the acidity of a carboxylic acid? | Increases acidity (stabilizes the RCOO− anion). |
| 42 | How does an Electron-Donating Group (EDG) affect the acidity of a carboxylic acid? | Decreases acidity (destabilizes the RCOO− anion). |
| 43 | Rank the acidity: F3CCOOH,Cl3CCOOH,CH3COOH. | F3CCOOH>Cl3CCOOH>CH3COOH (Stronger −I effect is more acidic). |
| 44 | How does the acidity of a substituted benzoic acid change with increasing distance of the EWG? | Decreases (Inductive effect diminishes with distance). |
| 45 | What is the product when a carboxylic acid reacts with an alcohol in the presence of an acid catalyst? | Ester (RCOOR′) (Esterification). |
| 46 | Is Esterification a reversible or irreversible reaction? | Reversible (water must be removed to drive the equilibrium forward). |
| 47 | What is the product when a carboxylic acid is reduced with LiAlH4? | Primary (1∘) alcohol. |
| 48 | What is the final product when Ethanoic Acid is treated with Cl2/Red P? | Chloroacetic Acid (ClCH2COOH) (Hell-Volhard-Zelinsky reaction). |
| 49 | What is the term for the reaction of a carboxylic acid with Br2/Red P? | Hell-Volhard-Zelinsky (HVZ) Reaction. |
| 50 | What part of the carboxylic acid is substituted in the HVZ reaction? | The α-hydrogen atom. |
| 51 | What is the general term for the reaction used to prepare amines by converting the COOH group to an NH2 group? | Decarboxylation (loss of CO2). |
| 52 | What is the purpose of heating a carboxylate salt with Soda Lime (NaOH+CaO)? | Decarboxylation (to form an alkane with one less carbon). |
Part 5: Aldol and Cannizzaro Reactions
| Q. No. | Question | Answer |
| 53 | What is the essential structural requirement for a compound to undergo Aldol Condensation? | Presence of at least one α-hydrogen atom. |
| 54 | What reagent is used to catalyze Aldol Condensation? | Dilute base (NaOH,Ba(OH)2, etc.). |
| 55 | What is the final stable product of the Aldol Condensation? | An α,β-unsaturated carbonyl compound (formed by dehydration of the aldol). |
| 56 | What is the name of the reaction between two different carbonyl compounds, both containing α-hydrogens? | Cross-Aldol Condensation. |
| 57 | What is the structural requirement for a compound to undergo Cannizzaro Reaction? | Absence of α-hydrogen atoms. |
| 58 | What reagent is used to catalyze the Cannizzaro Reaction? | Concentrated base (NaOH,KOH). |
| 59 | What type of reaction is the Cannizzaro reaction? | A Disproportionation (self-oxidation and reduction). |
| 60 | What are the two products formed when Formaldehyde undergoes the Cannizzaro reaction? | Methanol (Reduction) and Sodium Formate (Oxidation). |
| 61 | What is the name of the reaction between two different aldehydes, both lacking α-hydrogens? | Cross-Cannizzaro Reaction. |
| 62 | What is the reaction where a carbonyl compound reacts with an aromatic aldehyde? | Claisen-Schmidt Condensation (a type of cross-aldol). |
| 63 | Name the reaction where an aldehyde with no α−H reacts with an enolizable ketone. | Claisen-Schmidt Condensation. |
Part 6: Physical Properties and Miscellaneous Concepts
| Q. No. | Question | Answer |
| 64 | Why do carboxylic acids have higher boiling points than corresponding aldehydes, ketones, and even alcohols? | Extensive formation of Intermolecular Hydrogen Bonded Dimers. |
| 65 | What state (monomer or dimer) does Ethanoic Acid exist in the vapour phase? | Dimer (held by two H-bonds). |
| 66 | Why are lower aldehydes and ketones soluble in water? | They can form H-bonds with water molecules. |
| 67 | How does the solubility of aldehydes/ketones change with increasing size? | Decreases (due to increased non-polar hydrocarbon part). |
| 68 | What is the product when an aldehyde reacts with Hydrazine(NH2NH2)? | Hydrazone. |
| 69 | What is the product when an aldehyde reacts with Phenylhydrazine? | Phenylhydrazone. |
| 70 | What is Schiff's Reagent used for? | Distinguishing between aldehydes and ketones (Aldehydes restore the pink/magenta color). |
| 71 | What is the product of the reaction of an aldehyde with a Grignard Reagent followed by oxidation? | A secondary alcohol (from RCHO). |
| 72 | What is the term for the reaction of Benzaldehyde with Acyl Anhydride and Sodium Salt of the acid? | Perkin Reaction. |
| 73 | What is the product of the Perkin reaction? | α,β-unsaturated carboxylic acid (e.g., Cinnamic Acid). |
| 74 | What is the product when Ethanoic Acid is heated with P2O5? | Acetic Anhydride (CH3CO2O). |
| 75 | What is the product when Ethanoic Acid reacts with PCl5? | Acetyl Chloride (CH3COCl). |
| 76 | What is the name of the reaction where Benzaldehyde reacts with KCN to form benzoin? | Benzoin Condensation. |
| 77 | What is the role of the Cyanide ion (CN−) in the Benzoin Condensation? | It acts as a nucleophilic catalyst. |
| 78 | What compound is used commercially as a food preservative? | Sodium Benzoate (C6H5COONa). |
| 79 | What is the product when Ethanal reacts with Tollen’s Reagent? | Ammonium Acetate (CH3COONH4) and Ag mirror. |
| 80 | Why is Formalin solution used to preserve biological specimens? | It is an aqueous solution of Formaldehyde (≈40%). |
| 81 | Why is the Carbonyl Carbon considered an Electrophilic Center? | Due to the partial positive charge caused by the C=O polarity. |
| 82 | How many α-hydrogens are in Propanal (CH3CH2CHO)? | Two (on the C−2 carbon). |
| 83 | How many α-hydrogens are in Acetophenone (C6H5COCH3)? | Three (on the CH3 group). |
| 84 | Which is the only aldehyde that undergoes Cannizzaro Reaction exclusively? | Formaldehyde (HCHO). |
| 85 | Why is the Benzoyl group m-directing and deactivating in electrophilic substitution? | The C=O group is EWG, showing a strong −M effect. |
| 86 | What is the common name for Benzene-1,4-dicarboxylic acid? | Terephthalic Acid. |
| 87 | What is the product of the reaction of Formaldehyde with Ammonia? | Urotropine (Hexamethylenetetramine). |
| 88 | What is the major product when Butanal undergoes Aldol Condensation? | 2-Ethylhex-2-enal. |
| 89 | What is the pKa value used to express? | The strength of an acid (lower pKa is stronger acid). |
| 90 | What are Lactones? | Cyclic Esters formed from hydroxy acids. |
| 91 | What are Lactams? | Cyclic Amides. |
| 92 | What is the name of the reaction that converts a ketone to an ester using Peroxyacid? | Baeyer-Villiger Oxidation. |
| 93 | What is the role of the Tollens Reagent in the test for aldehydes? | It acts as a mild oxidising agent. |
| 94 | What is the product when Ethanal is oxidized by strong oxidizing agents like KMnO4? | Ethanoic Acid (CH3COOH). |
| 95 | What is the final product when Propanoic Acid undergoes HVZ reaction and subsequent hydrolysis? | α-Hydroxypropanoic Acid. |
| 96 | What is the key difference between Acyl Chlorides and Carboxylic Acids in terms of reactivity? | Acyl Chlorides are much more reactive toward nucleophilic attack (better leaving group, Cl−). |
| 97 | What is the product when Benzaldehyde is heated with conc.NaOH? | Benzyl Alcohol and Sodium Benzoate (Cannizzaro Reaction). |
| 98 | Why are Ketones used in the body for energy production during starvation? | They can be converted into Acetoacetate (ketone bodies) in the liver. |
| 99 | Name the reaction that is a combination of two Cannizzaro reactions occurring within the same molecule. | Intramolecular Cannizzaro Reaction. |
| 100 | What is the product when Acetone is treated with Ammonia followed by reduction? | Isopropylamine. |
| 101 | What is the product of Acetaldehyde reacting with a strong oxidizing agent like KMnO4? | Acetic Acid. |
| 102 | What is the common name for the reaction of Benzaldehyde with Aniline? | Formation of a Schiff's Base (Imine formation). |
| 103 | What is the most stable form of the Carboxylic Acid dimer in the solid state? | A ring structure held by two H-bonds. |
| 104 | Give the name of the product when Benzoyl Chloride reacts with water. | Benzoic Acid (Hydrolysis). |
| 105 | What is the final product of the reaction of an Aldehyde with Ammoniacal Silver Nitrate (Tollen’s)? | The salt of the carboxylic acid and elemental Silver. |
| 106 | Why does Benzoic Acid not undergo Friedel-Crafts reaction? | The -COOH group is a strong deactivating group (and complexes with the AlCl3 catalyst). |
| 107 | What is the intermediate formed during the Clemmensen reduction mechanism? | Generally involves a zinc amalgam intermediate. |
| 108 | What is the common use of Adipic Acid (Hexane-1,6-dioic acid)? | Manufacturing Nylon-6,6. |
| 109 | What is the order of reactivity in nucleophilic addition: Formaldehyde,Acetaldehyde,Acetone? | Formaldehyde>Acetaldehyde>Acetone. |
| 110 | Why is the Cannizzaro reaction preferred over Aldol at high base concentration? | The high base concentration favors the hydride ion transfer (disproportionation). |
| 111 | Name the reaction that converts a primary amide to a primary amine with one less carbon atom. | Hofmann Bromamide Degradation. |
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