Alcohols, Phenols and Ethers — Class 12 Maharashtra HSC Chemistry revision notes
A 6-page visual revision sheet for Alcohols, Phenols and Ethers, written for Class 12 Maharashtra HSC 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.
Page 1 as PDFA preview of page 1 — all 6 pages open full size in the app.
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 vs Ether
Alcohol
-OH on an sp^3 carbon: 1 deg, 2 deg, 3 deg by carbons that carbon touches
-OH on an sp^2 carbon of a C=C is a vinylic alcohol, not classed 1/2/3 deg
Phenol
-OH directly on an aromatic ring carbon
-OH on an sp^3 carbon attached to the ring is aromatic alcohol, benzylic, not phenol
Ether
O bonded to two alkyl and/or aryl groups, R-O-R', Ar-O-R, Ar-O-Ar'
symmetrical if both groups match, unsymmetrical (mixed) if they differ
Three Ways to Name an Alcohol
common/trivial: alkyl group name + word 'alcohol', e.g. isopropyl alcohol, tert-butyl alcohol
carbinol system: alcohols as substituted methyl alcohol (carbinol), groups named alphabetically first
IUPAC: alkane's -e becomes -ol, lowest locant to -OH
polyhydric alcohols keep the -e and add di-/tri-ol with locants: ethane-1,2-diol, propane-1,2,3-triol
Naming Phenols and Ethers
phenol's IUPAC name is benzenol, though 'phenol' itself is IUPAC-accepted
substituted phenols use o-/m-/p- or locants 2-/3-/4-: catechol is 1,2-diol, resorcinol 1,3-diol, hydroquinone 1,4-diol
common ether names: alkyl names alphabetically + 'ether' (di- if both match), e.g. ethyl methyl ether
IUPAC ether names: alkoxyalkane. LARGER group is the parent, smaller becomes alkoxy-, e.g. 2-methoxypropane
Page 1 of 6. The full sheet, all 6 pages, opens free in the app.
What this Alcohols, Phenols and Ethers sheet covers
Alcohol vs Phenol vs Ether
Alcohol
Phenol
Ether
Three Ways to Name an Alcohol
Naming Phenols and Ethers
Preparation of Alcohols
from alkyl halide, hydrolysis
acid-catalysed hydration of an alkene, Markovnikov
hydroboration-oxidation, B_2H_6 then H_2O_2/OH^-, anti-Markovnikov
reduction of an aldehyde/ketone with H_2/Ni or LiAlH_4
reduction of a carboxylic acid, LiAlH_4 only (H_2/Ni is too weak)
Reducing a Carbonyl: What Reagent, and What Survives
Grignard Addition: One Reagent, Any Class of Alcohol
Preparation of Phenol
Physical Properties and Hydrogen Bonding
Laboratory Tests
Why Phenol Beats Alcohol on Acidity
Alcohol, weaker acid
Phenol, stronger acid
Esterification and Acetyl Derivatives
Reactions That Break the C-O Bond
Oxidising an Alcohol: What You Get Depends on the Oxidant
These notes are not a standalone PDF. CapCompass plans Chemistry chapter by chapter against your real exam dates and free hours, and when the plan reaches Alcohols, Phenols and Ethers the sheet opens inside the study block itself — at the page covering the sub-topic that block is on, with the timer still running. Revision arrives at the moment the plan says revise, instead of having to be gone looking for.