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EXPERIMENT 22 Williamson Synthesis of Ethers

The solubility of Grignard reagents in ether plays a crucial role in their formation. The reagents are soluble [Pg.321]

Grignard reagents are normally insoluble in hydrocarbon solvents. However, they can be rendered soluble by the addition of a tertiary amine to the hydrocarbon-Grignard reagent mixture. Explain. [Pg.321]

For the many references related to the preparation and use of the Grignard reagent cited in Organic Syntheses, see the Reaction [Pg.321]

Indexes in Collected Volumes I-X under Grignard Reactions. [Pg.321]

Common names propyl p-tolyl ether, 4-propoxytoluene CA number [5349-18-8] [Pg.321]

EXPERIMENT 22 Williamson Synthesis of Ethers 329 300 MHz IH NMR SPECTRUM OF METHYL p-ETHYLPHENYL ETHER IN CDCI3... [Pg.329]

See other pages where EXPERIMENT 22 Williamson Synthesis of Ethers is mentioned: [Pg.321]    [Pg.323]    [Pg.325]    [Pg.327]    [Pg.331]    [Pg.333]    [Pg.335]    [Pg.337]    [Pg.321]    [Pg.323]    [Pg.325]    [Pg.327]    [Pg.331]    [Pg.333]    [Pg.335]    [Pg.337]   


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