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NCERT Chemistry: Alcohols, Phenols, and Ethers
Jul 9, 2024
One Shot: NCERT Related Information
Introduction
Focus: NCERT and more priority sections
Reaction mechanisms always exist, but it's not necessary to cover all mechanisms
Chapters included in One Shot
Alcohols, Phenols, and Ethers (NCERT 12th grade, second part)
Haloalkanes and Haloarenes information is also necessary because they are important in reactions
Alcohols, Phenols, and Ethers
Alcohols
Primary, Secondary, Tertiary alcohols
Monohydric, Dihydric, Trihydric alcohols
Phenols
Ethers
Alcohols
Classification
Number of O Groups
: Monohydric, Dihydric, Trihydric
Based on Degree
: 1┬░, 2┬░, 3┬░ alcohols
Based on Hybridization
: sp3 Carbon (Aliphatic, Benzylic) and sp2 Carbon (Aromatic Alcohol, Vinylic Alcohol)
Nomenclature
Common Name
and
IUPAC Name
: such as Methanol, Propanol, Butanol
Alcohols are named using the prefix hydroxy- and the suffix -ol
Preparation
Nucleophilic Substitution
: RX + NaOH тЖТ ROH + NaX
Addition of Water on Alkene
(Markovnikov's rule, Hydroboration Oxidation)
From Aldehyde/Ketone with Grignard Reagent
Reaction via Ester Hydrolysis
Dehydration of Alcohol
(Ether formation)
Commercial Methods
: Methanol, Ethanol industrial production
Reactions
Acidic Nature
: Donating H+ (R-OH тЖТ R-O- + H+)
Reaction with Metals
Lucas Test
: Identification of 1┬░, 2┬░, 3┬░ alcohols with HCl/ZnCl2
Esterification
HI as Reducing Agent
(with Thionyl chloride)
Oxidation
: using KMnO4, PCC, or hot copper for oxidation to aldehyde/ketone
Phenols
Preparation
Diazotization
: Apply special conditions (very high temperature and pressure)
Cumene process
: in laboratory
HBr and Sodium Hydroxide base process
Reactions
Acidic Nature
: Reactions with NaOH, Na, Zn, FeCl3
Ester formation
Does not undergo Friedel-Crafts Reaction
Ethers
Classification
Symmetrical Ethers
Unsymmetrical Ethers
Nomenclature
Common Names
: Dimethyl Ether, Ethyl Methyl Ether
IUPAC Names
: Methoxymethane, Methoxypropane
Preparation
Dehydration of Alcohol
: Williamson Synthesis
Diazomethane
: from alcohol in presence of SDH acid and BF3
Reactions
Reaction with HCl
Alpha Halogenation
Electrophilic Substitution
: at ortho and para positions
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