1. Physical chemistry
  2. 1. The solid state
    2. Language of Chemistry
    3. Gaseous and Liquid states
    4. Stoichiometry
    5. Solutions
    6. Structure of Atom
    7. Chemical equilibrium
    8. Nuclear chemistry (Radioactivity)
    9. Ionic equilibrium
    10. Chemical Bonding
    11. Chemical kinetics
    12. Concepts of Acids, Bases and Salts
    13. Surface catalysis and Colloids
    14. Redox reactions
    15. Chemical energetics
    16. Volumetric analysis
    17. Electrochemistry
  3. Inorganic chemistry
  4. 18. Introduction
    19. Periodic table
    20. Hydrogen and its compounds
    21. General aspects of Metallergy
    22. Alkali metals
    23. Alkaline metals
    24. Boron family
    25. Carbon family
    26. Nitrogen family
    27. Oxygen family
    28. Fluorine family
    29. Inert gases
    30. Transition metals
    31. Coordination compounds
    32. Analytical chemistry
  5. Organic chemistry
  6. 33. Purification and analysis of organic compounds
    34. Nomenclature of Organic compounds
    35. Reaction Mechanisms
    36. Hydrocarbons
    37. Haloalkanes (Alkyl halides)
    38. Alcohol, Phenol and Ether
    39. Aldehyde and Ketones
    40. Carboxylic acids
    41. Compounds conatining Nitrogen
    42. Polymers
    43. Chemistry in daily life
Organic chemistry
38. Alcohol, Phenol and Ether
1. Which of the following when reacted with water produces phenol?

[IOM 2007]

  • C₆H₅N= NCl
  • C₆H₅−Cl
  • C₆H₅CH₂Cl
  • C₆H₅−CHO
2. Reduction of aldehyde gives

[IOM 2001]

  • Acid
  • Alcohol
  • Ester
  • Alkyne
3. Percentage of water in absolute alcohol is
  • 5%
  • 3%
  • 10%
  • Zero
4. Alcohol poisoning occurs due to the presence of .... in alcohol that is used for drinking.

[IOM 2005]

  • Carbonic acid
  • Ethyl alcohol
  • Methyl alcohol
  • Impurities (HCN + HCOOH)
5. The reactivity of alcohol with Lucas reagent follows the order

[MOE 2008]

  • 1° > 2° > 3°
  • 3° > 2° > 1°
  • 2° > 1° > 3°
  • Same for all
6. When ethyl alcohol is treated with acidified potassium dichromate it forms acetaldehyde. It is an example of

[MOE 2064 Aswin]

  • Molecular rearrangement
  • Hydrolysis
  • Oxidation
  • Reduction
7. Which enzyme is used during the production of alcohol from carbohydrate by fermentation?

[MOE 2064]

  • Invertase
  • Zymase
  • Starch
  • Molasses
8. Hydrolysis of table sugar produces

[MOE - Curriculum]

  • Two molecules of Glucose
  • Glucose and Fructose
  • Glucose and Galactose
  • Glucose and Lactose
9. Which of the following alcohol is most reactive towards Lucas reagent?

[Bangladesh Embassy]

  • Primary
  • Secondary
  • Tertiary
  • Same for all
10. 1°, 2° and 3° alcohols are distinguished by all of the following methods except

[IOM 2051]

  • Lucas test
  • Victor Meyer test
  • Oxidation test
  • Hoffmann method
11. 2C₂H₅OH + 2Na → 2C₂H₅ONa + H₂. The above reaction shows

[IOM 2053]

  • Acidic nature of Na
  • The acidic nature of C₂H₅OH
  • Oxidizing action of Na
  • Reducing action of C₂H₅OH
12. Glycerol contains ......... alcoholic group.

[TOM 2046]

  • 3 primary
  • 1 primary
  • 1 primary and 2 secondary
  • 2 primary and 1 secondary
13. Grignard reagent is
  • Mg(OH)₂
  • Alkyl halides
  • Alkyl magnesium halides
  • MgCl
14. Methylamine when treated with HNO₂ results into

[MOE 2054]

  • Methyl cyanide
  • Acetic acid
  • Methyl isocyanate
  • Methanol
15. On passing ethene through alkaline solution of KMnO₄ (Baeyer's reagent) the compound formed is

[IOM 205]

  • Ethyl alcohol
  • Ethylene glycol
  • Oxalic acid
  • Formaldehyde
16. Primary, secondary and tertiary alcohol are distinguished by

[IOM 2052]

  • Distillation
  • Victor Meyer method
  • Hoffmann method
  • Reimer Tiemann reaction
17. Reaction between NaOH and fat is called
  • Esterification
  • Rancification
  • Hydrogenation
  • Saponification
18. RCHO reacts with RMgBr and the product of hydrolysis yields

[IOM 2046]

  • Primary alcohol
  • Secondary alcohol
  • Tertiary alcohol
  • Acetone
19. The alkaline solution of 1% KMnO₄ is called

[MOE 2053]

  • Schiff's reagent
  • Fehling's solution
  • Tollen's reagent
  • Baeyer's reagent
20. Conversion of glucose or fructose into ethyl alcohol is brought about by

[IOM, MOE, KU, BPKIHS]

  • Invertase
  • Diastase
  • Maltase
  • Zymase
PHENOL
1. When -OH group is linked with benzene, the compound formed is

[IOM 2000]

  • Phenol
  • Benzaldehyde
  • Benzyl alcohol
  • Acetophenone
2. Which of the following compound when reacted with water produces Phenol?

[IOM 2007]

  • C₆H₅N₂Cl
  • C₆H₅Cl
  • C₆H₅CH₂Cl
  • C₆H₅CHO
3. Phenol on distillation with zinc dust gives

[IOM, MOE]

  • Benzaldehyde
  • Benzene
  • Benzoic acid
  • Cyclohexane
4. Phenol reacts with PCl₅ to give mainly

[OM]

  • p-Chlorophenol
  • Chlorobenzene
  • o- and p-Chlorophenols
  • Triphenylphosphate
5. Phenol reacts with Br₂ in CCl₄ at low temperature gives

[MOE]

  • m-Bromophenol
  • o- and p-Bromophenol
  • p-Bromophenol
  • 2,4,6-Tribromophenol
ETHER
1. When ethyl hydrogen sulphate is heated with excess of alcohol at 410 K, the product obtained is
  • Ethane
  • Ethylene
  • Diethyl ether
  • Diethyl sulphate
2. Anisole with conc. HNO₃ and conc. H₂SO₄ gives
  • Phenol
  • Nitrobenzene
  • o- and p-Nitroanisole
  • m-Nitroanisole
3. When a 1° alkyl halide reacts with an alkoxide, the product is
  • Hydrocarbon
  • Ether
  • Unsaturated hydrocarbon
  • Alcohol
4. Which of the following cannot be prepared by using Williamson's synthesis?
  • Methoxybenzene
  • Benzyl-p-nitrophenyl ether
  • Methyl tert-butyl ether
  • Di-tertiary butyl ether
5. Which of the following compounds is resistant to nucleophilic attack by OH⁻ ions?
  • Urea
  • Acetonitrile
  • Acetamide
  • Diethyl ether
6. How many isomeric ethers are represented by the molecular formula C₄H₁₀O?
  • 3
  • 2
  • 4
  • 5
7. In Williamson synthesis, ethoxyethane is prepared by
  • Passing ethanol over alumina
  • Heating ethanol with dry Ag₂O
  • Heating sodium ethoxide with ethyl bromide
  • Treating ethyl alcohol with excess of H₂SO₄ at 443 K
8. An aromatic ether is not cleaved by HI even at 525 K. The compound is
  • C₆H₅OCH₃
  • C₆H₅OC₆H₅
  • C₆H₅OC₃H₇
  • Tetrahydrofuran
9. Ether is obtained from ethyl alcohol
  • In presence of H₂SO₄ at 413 K
  • In presence of H₂SO₄ at 473 K
  • In presence of H₂SO₄ at 383 K
  • In presence of H₂SO₄ at 273 K
10. Acetic anhydride reacts with diethyl ether in the presence of anhydrous AlCl₃ to give
  • CH₃COOCH₃
  • CH₃CH₂COOCH₃
  • CH₃COOCH₂CH₃
  • CH₃CH₂OH
11. Which of the following compounds on boiling with alkaline KMnO₄ and subsequent acidification will not give benzoic acid?
  • Toluene
  • Acetophenone
  • Anisole
  • Benzyl alcohol
12. An organic compound of molecular formula C₃H₆O does not produce any precipitate with 2,4-dinitrophenylhydrazine and does not react with sodium metal. This compound is
  • CH₃COCH₃
  • CH₂=CH−OCH₃
  • CH₃CH₂CHO
  • CH₂=CHCH₂OH
13. The C−O−C angle in ether is about
  • 180°
  • 190°28′
  • 110°
  • 105°
14. The ether that undergoes electrophilic substitution reactions is
  • CH₃OC₂H₄
  • C₆H₅OCH₃
  • CH₃OCH₃
  • C₂H₅OC₂H₅
15. Anisole with HNO₃ and conc. H₂SO₄ gives
  • Phenol
  • Nitrobenzene
  • o- and p-Nitroanisoles
  • o-Nitroanisole
16. Ether which is liquid at room temperature is
  • C₂H₅OCH₃
  • CH₃OCH₃
  • C₂H₅OC₂H₅
  • None
17. An ether is more volatile than an alcohol having the same molecular formula. This is due to
  • Dipolar character of ethers
  • Alcohols having resonance structure
  • Intermolecular hydrogen bonding in ethers
  • Intermolecular hydrogen bonding in alcohols
18. When methyl-tert-butyl ether is formed?
  • (C₂H₅)₃CONa + CH₃Cl
  • CH₃ONa + (CH₃)₃CCl
  • (CH₃)₃CONa + C₂H₅Cl
  • (CH₃)₃CONa + CH₃Cl
19. Alcohols are isomeric with

[IOM 2010]

  • Acids
  • Ethers
  • Esters
  • Aldehydes
20. Williamson's synthesis is an example of
  • Nucleophilic addition
  • Electrophilic addition
  • Electrophilic substitution
  • Nucleophilic substitution
21. Which of the following process is used in the preparation of ether?

[MOE]

  • Wurtz reaction
  • Kolbe's synthesis
  • Williamson's synthesis
  • Hoffmann synthesis
22. Williamson's synthesis is used to prepare

[MOE]

  • Only symmetrical ethers
  • Only asymmetrical ethers
  • Both
  • None
23. Ethers on hydrolysis give
  • Carboxylic acids
  • Alcohols
  • Esters
  • Ketones
24. Ethers can be used as
  • General anaesthetic
  • Refrigerant
  • In perfumery
  • All of the above
25. Heating methyl phenyl ether with HI gives
  • Methanol + Iodobenzene
  • Methyl iodide + Iodobenzene
  • Methyl alcohol + Benzyl alcohol
  • Methyl iodide + Phenol
26. Higher homologues of ether can be prepared by
  • Alkyl halides
  • Diazomethane
  • Grignard reagent
  • None of these