The -OH group in phenol activates the benzene ring towards electrophilic substitution and directs incoming groups to ortho and para positions due to the electron-rich nature of these positions caused by resonance effects from the -OH group.

Tertiary alcohols do not undergo oxidation reactions. Under strong conditions (KMnO₄) and elevated temperatures, cleavage of various C-C bonds occurs, leading to a mixture of carboxylic acids with fewer carbon atoms.

PCC is a milder reagent for oxidizing primary alcohols to aldehydes. Secondary alcohols are oxidized to ketones using chromic anhydride (CrO₃).

Dehydrogenation occurs in alcohol oxidation, involving the cleavage of O-H and C-H bonds. Primary alcohols oxidize to aldehydes or carboxylic acids, depending on the oxidizing agent. Strong agents like acidified potassium permanganate yield carboxylic acids directly.

Dehydration of alcohols, leading to the formation of alkenes, occurs with protic acids (e.g., concentrated H₂SO₄ or H₃PO₄) or catalysts like anhydrous zinc chloride or alumina. The relative ease of dehydration follows the order: Tertiary > Secondary > Primary.

Phosphorus tribromide is used to convert alcohols to alkyl bromides. This reaction differs from the Lucas test, offering an alternative method for the transformation of alcohols into halides.

Alcohols react with hydrogen halides to form alkyl halides. The Lucas test, using Lucas reagent (conc. HCl and ZnCl₂), distinguishes between alcohol classes based on the time taken for turbidity to appear; tertiary alcohols show immediate turbidity, while primary alcohols ...

Alkenes undergo acid-catalyzed hydration in the presence of water and acid catalyst, forming alcohols. In the case of unsymmetrical alkenes, the addition follows Markovnikov’s rule.

In ethers, the four electron pairs on oxygen, two bond pairs and two lone pairs, are arranged approximately tetrahedrally. The bond angle is slightly greater than the tetrahedral angle due to repulsive interactions between the two bulky (–R) groups attached ...

In phenol, the carbon–oxygen bond length is shorter (136 pm) than in methanol due to partial double bond character resulting from the conjugation of the unshared electron pair of oxygen with the aromatic ring and the sp² hybridization of the ...