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Alcohols, Phenols and Ethers — Class 12 CBSE Chemistry revision notes

A 4-page visual revision sheet for Alcohols, Phenols and Ethers, written for Class 12 CBSE Chemistry. Formulas, diagrams and the traps that cost marks, laid out to be read the night before rather than the term before. Free, and it opens inside CapCompass.

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Alcohols, Phenols and Ethers in one look

the same -OH group behaves differently on a chain than on a ring, and an ether just hides the OH between two carbons

Alcohol vs phenol

Alcohol
  • -OH on an sp^3 carbon, e.g. CH_3CH_2OH
  • classified 1°, 2°, 3° by the carbon it sits on
  • weaker acid than phenol; the alkyl group pushes electron density onto oxygen
Phenol
  • -OH directly on an aromatic ring carbon
  • the O lone pair conjugates into the ring, so the O-H bond is more polarised
  • stronger acid than an alcohol; the phenoxide ion formed is resonance-stabilised across the ring

Classification and nomenclature

  • 1°/2°/3°: named by carbons on the carbinol carbon (bearing -OH), same as haloalkane classification
  • IUPAC name: replace alkane's -e with -ol, number chain for -OH's lowest locant
  • a diol has two -OH groups (e.g. ethylene glycol), a triol has three (e.g. glycerol)
  • ethers are named as alkoxyalkanes, e.g. CH_3-O-CH_2CH_3 is methoxyethane

Preparation of alcohols

  • from an alkyl halide, aqueous NaOH/KOH, SN2 R-X+NaOHto R-OH+NaX
  • from a Grignard reagent + formaldehyde, then aqueous acid workup R-MgX+HCHOto RCH_2-OMgXto RCH_2OH
  • from an alkene, acid-catalysed hydration (Markovnikov) R-CH=CH_2+H_2Oto R-CH(OH)-CH_3

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