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Chemistry notes on Alcohols, Phenols, and Ethers, conceptual and equation-free,

Sujoy Das
16 hrs ago 0 0

Class 12 Chemistry – Alcohols, Phenols, and Ethers


1. Alcohols

Definition

  • Alcohols are organic compounds in which one or more hydroxyl (-OH) groups are attached to a saturated carbon atom (sp³ hybridized).

  • Also called alkanols.

Classification

  • Primary (1°): -OH attached to a carbon bonded to one other carbon.

  • Secondary (2°): -OH attached to a carbon bonded to two other carbons.

  • Tertiary (3°): -OH attached to a carbon bonded to three other carbons.

Physical Properties

  • State: Usually liquids (methanol, ethanol)

  • Solubility: Soluble in water due to hydrogen bonding

  • Boiling Point: Higher than alkanes due to hydrogen bonding

Chemical Properties

  • Combustion: Burn to produce CO₂ and water

  • Oxidation: Can produce aldehydes, ketones, or acids depending on type

  • Dehydration: Can lose water to form alkenes

  • Reaction with acids and halides: Forms haloalkanes or esters


2. Phenols

Definition

  • Phenols are compounds in which a hydroxyl (-OH) group is directly attached to an aromatic ring (like benzene).

Physical Properties

  • State: Usually solids or liquids

  • Solubility: Moderately soluble in water due to hydrogen bonding

  • Boiling Point: Higher than hydrocarbons but lower than alcohols

Chemical Properties

  • Acidic nature: Phenols are weakly acidic, can react with bases to form salts

  • Electrophilic substitution: Substitutions occur on the aromatic ring, usually at ortho and para positions

  • Oxidation: Can produce quinones

Applications

  • Used in disinfectants, antiseptics, resins, and dyes


3. Ethers

Definition

  • Ethers are compounds in which an oxygen atom is bonded to two carbon atoms (R–O–R').

Physical Properties

  • State: Usually liquids

  • Solubility: Slightly soluble in water, more soluble in organic solvents

  • Boiling Point: Lower than alcohols of similar mass (no hydrogen bonding)

Chemical Properties

  • Relatively less reactive due to absence of -OH hydrogen

  • Can undergo cleavage with strong acids

  • Used as solvents, anesthetics, and intermediates in chemical reactions


4. Key Differences Between Alcohols, Phenols, and Ethers

Feature Alcohols Phenols Ethers
Functional group -OH on sp³ carbon -OH on aromatic ring Oxygen between carbons (R–O–R')
Acidity Weakly acidic More acidic Neutral
Hydrogen bonding Present Present Absent (only dipole)
Reactivity Moderate Reactive in aromatic substitutions Relatively low
Solubility High Moderate Low to moderate

5. Applications

  • Alcohols: Solvents, fuels (ethanol, methanol), beverages, antiseptics

  • Phenols: Disinfectants, antiseptics, resins, dyes

  • Ethers: Solvents, anesthetics, intermediates in organic synthesis

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