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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. Template reaction - Wikipedia

    en.wikipedia.org/wiki/Template_reaction

    18-Crown-6 can be synthesized by the Williamson ether synthesis using potassium ion as the template cation. Structure of nickel-aquo nitrate complex of the ligand derived from the templated trimerization of 2-aminobenzaldehyde. [5] The phosphorus analogue of an aza crown can be prepared by a template reaction. [6]

  5. 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]

  6. 1,2-Wittig rearrangement - Wikipedia

    en.wikipedia.org/wiki/1,2-Wittig_rearrangement

    A 1,2-Wittig rearrangement is a categorization of chemical reactions in organic chemistry, and consists of a 1,2-rearrangement of an ether with an alkyllithium compound. [1] The reaction is named for Nobel Prize winning chemist Georg Wittig. [2] [3] The intermediate is an alkoxy lithium salt, and the final product an alcohol.

  7. Piperonal - Wikipedia

    en.wikipedia.org/wiki/Piperonal

    Synthesis from the latter chemical is accomplished through a condensation reaction with glyoxylic acid followed by cleaving the resulting α-hydroxy acid with an oxidizing agent. [ 3 ] [ 4 ] [ 5 ] Synthesis from catechol requires an additional step, Williamson ether synthesis using dichloromethane .

  8. Pregnant Alex Morgan Reveals Her Daughter's Hilarious ... - AOL

    www.aol.com/pregnant-alex-morgan-reveals-her...

    When Alex Morgan received her lookalike Barbie doll, she was excited to show her daughter — until she saw her reaction.. The retired soccer star, who is currently pregnant with her second baby ...

  9. 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.