Alcohols phenols ethers aldehydes ketones carboxylic acids preparation properties reactions and important tests - One Line Questions

1. Which functional group is present in a ketone? -CO-
2. Which functional group defines a carboxylic acid? -COOH
3. Which functional group defines an alcohol? -OH
4. Which functional group characterizes an aldehyde? -CHO
5. What is the common name for methanal? Formaldehyde
6. What is the product when acetaldehyde reacts with HCN? Acetaldehyde cyanohydrin
7. What is the common name for propanone? Acetone
8. The product of the iodoform test is a yellow precipitate of: CHI3
9. The Kolbe reaction is used for the carboxylation of: Phenols
10. What product is formed when a secondary alcohol is oxidized? Ketone
11. The Clemmensen reduction is used to reduce: Aldehydes and ketones to alkanes
12. Which type of compounds give a positive iodoform test? Ketones with at least one methyl group attached to the carbonyl carbon
13. What is the Hell-Volhard-Zelinsky (HVZ) reaction used for? Alpha-halogenation of carboxylic acids
14. Williamson ether synthesis involves the reaction between: An alkoxide and a primary alkyl halide
15. Fehling's solution consists of two solutions: A and B. Solution A is: Aqueous solution of CuSO4
16. What is the primary use of ethanol in industry? As a precursor for other chemicals
17. The Reimer-Tiemann reaction is used to introduce an aldehyde group onto the ring of: Phenol
18. The reaction of an aldehyde with sodium bisulfite forms a: Bisulfite addition product
19. What is the common name for phenol? Carbolic acid
20. What is the IUPAC name for CH3OCH3? Dimethyl ether
21. Which of the following reactions is characteristic of phenols and not alcohols? Electrophilic aromatic substitution
22. Which alcohol is known as wood alcohol? Methanol
23. Which compound gives a positive test with sodium bicarbonate solution? Acetic acid
24. The reaction of an aldehyde or ketone with a Grignard reagent followed by hydrolysis produces: Alcohol
25. What is the product of esterification of a carboxylic acid with an alcohol in the presence of an acid catalyst? Ester
26. What is the observation in Tollens' test when an aldehyde is present? Formation of a silver mirror
27. What is the observation in Fehling's test when an aldehyde is present? Formation of a red precipitate of Cu2O
28. What is the IUPAC name for CH3COOH? Acetic acid
29. The Cannizzaro reaction is shown by aldehydes that: Lack alpha-hydrogens
30. What is the IUPAC name for CH3CHO? Ethanal
31. Which of the following alcohols is used as an antifreeze? Ethylene glycol
32. What is the IUPAC name for CH3CH2OH? Ethanol
33. The reaction of phenols with bromine water results in: Tribromophenol
34. Which reaction is characteristic of aldehydes but not ketones? Oxidation by mild oxidizing agents
35. Which of the following is a characteristic reaction of ethers? Cleavage by strong acids
36. Which of the following is a method for preparing ethers? Dehydration of alcohols
37. Which method is commonly used for the industrial preparation of ethanol? Fermentation of sugars
38. What is the main product when phenol reacts with phosgene (COCl2)? Phenyl chloroformate
39. Which type of alcohol has the hydroxyl group attached to a primary carbon atom? Primary alcohol
40. Which alcohol reacts fastest with Lucas reagent? Tertiary alcohol
41. Which of the following alcohols can be prepared by the reduction of a carboxylic acid? Primary alcohols
42. What is the IUPAC name for CH3COCH3? Propanone
43. Which of the following is an ether functional group? R-O-R'
44. Phenols are more acidic than alcohols due to: Resonance stabilization of the phenoxide ion
45. Tollens' reagent is an alkaline solution of: Ammoniacal silver nitrate
46. Tertiary alcohols cannot be easily oxidized by mild oxidizing agents because: They lack a hydrogen atom on the carbon bearing the hydroxyl group
47. What is the Lucas reagent used for? To distinguish between primary, secondary, and tertiary alcohols
48. Which test can distinguish between an aldehyde and a ketone? Both Tollens' and Fehling's tests
49. How are primary alcohols oxidized to aldehydes, and then further to carboxylic acids? Using strong oxidizing agents like KMnO4 or K2Cr2O7
50. Which reagent is used in the Wolff-Kishner reduction? Hydrazine and strong base