ROUTERA


Chapter 11 Alcohols, Phenols and Ethers

Class 12th Chemistry Chapter Case Study


Case Study 1: Alcohols and Their Preparation

Case: Alcohols are organic compounds containing one or more hydroxyl groups (-OH) attached to a carbon atom. They are classified into primary, secondary, and tertiary alcohols based on the number of alkyl groups attached to the carbon bearing the hydroxyl group. Alcohols can be prepared by various methods, including hydration of alkenes, reduction of aldehydes and ketones, and from alkyl halides by nucleophilic substitution reactions.

For instance, ethanol (C₂H₅OH) can be synthesized from ethene (C₂H₄) via an acid-catalyzed hydration reaction, where the alkene reacts with water in the presence of a catalyst such as sulfuric acid.

Questions:

  1. Ethanol (C₂H₅OH) is commonly prepared by the hydration of:

    • A) Propene
    • B) Butene
    • C) Ethene
    • D) Methane
    • Answer: C) Ethene
  2. The reaction of ethene with water in the presence of sulfuric acid to form ethanol is an example of:

    • A) Addition reaction
    • B) Substitution reaction
    • C) Oxidation reaction
    • D) Reduction reaction
    • Answer: A) Addition reaction
  3. In the preparation of alcohols from alkyl halides, the nucleophilic substitution reaction occurs in the presence of:

    • A) Acid
    • B) Base
    • C) Alcohol
    • D) Water
    • Answer: B) Base
  4. Primary alcohols are characterized by having:

    • A) One alkyl group attached to the carbon bearing the -OH group
    • B) Two alkyl groups attached to the carbon bearing the -OH group
    • C) Three alkyl groups attached to the carbon bearing the -OH group
    • D) No alkyl groups attached to the carbon bearing the -OH group
    • Answer: A) One alkyl group attached to the carbon bearing the -OH group

Case Study 2: Reactions of Alcohols

Case: Alcohols undergo several important reactions. They can be oxidized to form aldehydes, ketones, and carboxylic acids. The oxidation of primary alcohols results in aldehydes, and further oxidation leads to carboxylic acids. Secondary alcohols, on the other hand, are oxidized to ketones. Tertiary alcohols are generally resistant to oxidation due to the absence of a hydrogen atom attached to the carbon bearing the hydroxyl group.

For example, the oxidation of ethanol (CH₃CH₂OH) with an oxidizing agent like potassium dichromate (K₂Cr₂O₇) results in the formation of ethanal (acetaldehyde, CH₃CHO).

Questions:

  1. The oxidation of ethanol (CH₃CH₂OH) with K₂Cr₂O₇ results in the formation of:

    • A) Ethanol
    • B) Ethanal (acetaldehyde)
    • C) Acetic acid
    • D) Methanol
    • Answer: B) Ethanal (acetaldehyde)
  2. The oxidation of primary alcohols like ethanol produces:

    • A) Aldehydes
    • B) Ketones
    • C) Carboxylic acids
    • D) Ethers
    • Answer: A) Aldehydes
  3. Secondary alcohols are oxidized to form:

    • A) Aldehydes
    • B) Ketones
    • C) Carboxylic acids
    • D) Alcohols
    • Answer: B) Ketones
  4. Which of the following alcohols cannot be oxidized easily?

    • A) Primary alcohol
    • B) Secondary alcohol
    • C) Tertiary alcohol
    • D) All alcohols can be oxidized easily
    • Answer: C) Tertiary alcohol

Case Study 3: Phenols and Their Properties

Case: Phenols are compounds in which a hydroxyl group (-OH) is directly attached to an aromatic ring. Phenols are more acidic than alcohols due to the ability of the phenoxide ion to stabilize the negative charge through resonance with the aromatic ring. Common examples of phenols include hydroquinone (1,4-dihydroxybenzene), which is used in the manufacture of plastics and as a reducing agent, and salicylic acid, which is the precursor for aspirin.

Phenols undergo electrophilic substitution reactions, such as halogenation, nitration, and sulfonation, where the hydroxyl group increases the electron density on the benzene ring, making it more reactive towards electrophiles.

Questions:

  1. The hydroxyl group in phenols is attached to:

    • A) An alkyl group
    • B) An aromatic ring
    • C) An alkene group
    • D) A carbonyl group
    • Answer: B) An aromatic ring
  2. Phenols are more acidic than alcohols because:

    • A) The hydroxyl group is more electronegative
    • B) The phenoxide ion is stabilized by resonance
    • C) The -OH group is more polar
    • D) Phenols are less volatile than alcohols
    • Answer: B) The phenoxide ion is stabilized by resonance
  3. The electrophilic substitution reaction of phenol with bromine (Br₂) results in the formation of:

    • A) Phenol bromide
    • B) Bromobenzene
    • C) 2,4,6-Tribromophenol
    • D) Salicylic acid
    • Answer: C) 2,4,6-Tribromophenol
  4. Salicylic acid is the precursor to which of the following drugs?

    • A) Paracetamol
    • B) Ibuprofen
    • C) Aspirin
    • D) Morphine
    • Answer: C) Aspirin

Case Study 4: Ethers and Their Properties

Case: Ethers are organic compounds in which two alkyl or aryl groups are bonded to an oxygen atom, with the general formula R–O–R'. Ethers are relatively non-reactive but can be used as solvents for reactions involving non-polar substances. One of the most common ethers is diethyl ether (C₂H₅OC₂H₅), which is often used as a solvent in laboratories.

Ethers are relatively resistant to oxidation but undergo cleavage in the presence of strong acids to form alcohols or alkyl halides. For example, when diethyl ether is treated with excess HI, it undergoes cleavage to form ethanol and ethyl iodide.

Questions:

  1. The general formula of an ether is:

    • A) R–OH
    • B) R–O–R'
    • C) R–COOH
    • D) R–C=O
    • Answer: B) R–O–R'
  2. Diethyl ether (C₂H₅OC₂H₅) undergoes cleavage with excess HI to form:

    • A) Ethanol and ethyl iodide
    • B) Ethene and water
    • C) Ethanol and hydrogen iodide
    • D) Acetone and ethyl iodide
    • Answer: A) Ethanol and ethyl iodide
  3. Ethers are used as solvents because:

    • A) They are highly reactive
    • B) They dissolve both polar and non-polar compounds
    • C) They are acidic in nature
    • D) They are easily oxidized
    • Answer: B) They dissolve both polar and non-polar compounds
  4. Ethers are relatively resistant to oxidation but undergo cleavage in the presence of:

    • A) Strong acids
    • B) Strong bases
    • C) Light
    • D) Ozone
    • Answer: A) Strong acids

Case Study 5: Industrial Uses of Alcohols, Phenols, and Ethers

Case: Alcohols, phenols, and ethers are widely used in various industries. Alcohols like ethanol are used as solvents, fuels, and in the preparation of alcoholic beverages. Ethanol is also used in the production of plastics and pharmaceuticals. Phenols are used in the manufacture of resins, antiseptics, and in the synthesis of dyes. Ethers are primarily used as solvents in laboratories and as anesthetics. For instance, diethyl ether was historically used as a general anesthetic due to its ability to induce unconsciousness.

Questions:

  1. Ethanol is used in the production of:

    • A) Soap
    • B) Solvents
    • C) Plastics and pharmaceuticals
    • D) Both B and C
    • Answer: D) Both B and C
  2. Which of the following is an industrial use of phenol?

    • A) Production of resins
    • B) Manufacture of ethanol
    • C) As a solvent for dyes
    • D) As a refrigerant
    • Answer: A) Production of resins
  3. Diethyl ether is commonly used in:

    • A) Solvents in laboratories
    • B) General anesthesia
    • C) Cleaning agents
    • D) Both A and B
    • Answer: D) Both A and B
  4. Alcohols, phenols, and ethers are primarily used in industry due to their:

    • A) High reactivity
    • B) Ability to dissolve a wide range of substances
    • C) Low boiling points
    • D) Ability to resist oxidation
    • Answer: B) Ability to dissolve a wide range of substances