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  2. Williamson ether synthesis - Wikipedia

    en.wikipedia.org/wiki/Williamson_ether_synthesis

    The Williamson ether synthesis is an organic reaction, forming an ether from an organohalide and a deprotonated alcohol . This reaction was developed by Alexander Williamson in 1850. [ 2 ] Typically it involves the reaction of an alkoxide ion with a primary alkyl halide via an S N 2 reaction .

  3. Alexander William Williamson - Wikipedia

    en.wikipedia.org/wiki/Alexander_William_Williamson

    Alexander Williamson. Williamson is credited for his research on the formation of unsymmetrical ethers by the interaction of an alkoxide with a haloalkane, known as the Williamson ether synthesis. He regarded ethers and alcohols as substances analogous to and built up on the same type as water, and he further introduced the water-type as a ...

  4. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    Usually phenol ethers are synthesized through the condensation of phenol and an organic alcohol; however, other known reactions regarding the synthesis of ethers can be applied to phenol ethers as well. Anisole (C 6 H 5 OCH 3) is the simplest phenol ether, and is a versatile precursor for perfumes and pharmaceuticals. [1]

  5. Sodium phenoxide - Wikipedia

    en.wikipedia.org/wiki/Sodium_phenoxide

    Sodium phenoxide reacts with alkylating agents to afford alkyl phenyl ethers: [2] NaOC 6 H 5 + RBr → ROC 6 H 5 + NaBr. The conversion is an extension of the Williamson ether synthesis. With acylating agents, one obtains phenyl esters: [citation needed] NaOC 6 H 5 + RC(O)Cl → RCO 2 C 6 H 5 + NaCl

  6. Macrocyclic ligand - Wikipedia

    en.wikipedia.org/wiki/Macrocyclic_ligand

    When the metal atom is not desired in the final product, a disadvantage of templated synthesis is the difficulty in removing the templating metal from the macrocyclic ligand. 18-Crown-6 can be synthesized by the Williamson ether synthesis using potassium ion as the template cation.

  7. 15-Crown-5 - Wikipedia

    en.wikipedia.org/wiki/15-Crown-5

    15-Crown-5 is a crown ether with the formula (C 2 H 4 O) 5. It is a cyclic pentamer of ethylene oxide that forms complex with various cations , including sodium (Na + ) [ 2 ] and potassium (K + ); [ 3 ] however, it is complementary to Na + and thus has a higher selectivity for Na + ions.

  8. Supreme Court unanimous ruling may pave way for mass deportation

    www.aol.com/supreme-court-unanimous-ruling-may...

    (The Center Square) – A unanimous ruling by the U.S. Supreme Court may pave the way for challenges to a federal deportation plan under the incoming Trump administration to be defeated.

  9. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    The word's meaning became restricted to "spirit of wine" (the chemical known today as ethanol) in the 18th century and was extended to the class of substances so-called as "alcohols" in modern chemistry after 1850. [16] The term ethanol was invented in 1892, blending "ethane" with the "-ol" ending of "alcohol", which was generalized as a libfix ...