enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Michelson–Morley experiment - Wikipedia

    en.wikipedia.org/wiki/Michelson–Morley_experiment

    [A 2] Of this experiment, Albert Einstein wrote, "If the Michelson–Morley experiment had not brought us into serious embarrassment, no one would have regarded the relativity theory as a (halfway) redemption." [A 3]: 219 Michelson–Morley type experiments have been repeated many times with steadily increasing sensitivity.

  3. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    In accordance with an E2 elimination the reaction with t-butyl chloride results in a KIE of 2.3. The methyl chloride reaction (only S N 2 possible) on the other hand has a KIE of 0.85 consistent with a S N 2 reaction because in this reaction type the C-H bonds tighten in the transition state. The KIE's for the ethyl (0.99) and isopropyl (1.72 ...

  4. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    The classic example of a dehydration reaction is the Fischer esterification, which involves treating a carboxylic acid with an alcohol to give an ester RCO 2 H + R′OH ⇌ RCO 2 R′ + H 2 O. Often such reactions require the presence of a dehydrating agent, i.e. a substance that reacts with water.

  5. Ether - Wikipedia

    en.wikipedia.org/wiki/Ether

    A typical example of the first group is the solvent and anaesthetic diethyl ether, commonly referred to simply as "ether" (CH 3 −CH 2 −O−CH 2 −CH 3). Ethers are common in organic chemistry and even more prevalent in biochemistry, as they are common linkages in carbohydrates and lignin. [2]

  6. Elution - Wikipedia

    en.wikipedia.org/wiki/Elution

    Elution principle of column chromatography. In analytical and organic chemistry, elution is the process of extracting one material from another by washing with a solvent: washing of loaded ion-exchange resins to remove captured ions, or eluting proteins or other biopolymers from a gel electrophoresis or chromatography column.

  7. 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.

  8. Aldol condensation - Wikipedia

    en.wikipedia.org/wiki/Aldol_condensation

    However, this problem can be avoided if one of the compounds does not contain an α-hydrogen, rendering it non-enolizable. In an aldol condensation between an aldehyde and a ketone, the ketone acts as the nucleophile, as its carbonyl carbon does not possess high electrophilic character due to the +I effect and steric hindrance. Usually, the ...

  9. Talk:Michelson–Morley experiment/Archive 2 - Wikipedia

    en.wikipedia.org/wiki/Talk:Michelson–Morley...

    Example (from oldid 491686307), bold indicates problems: Starting in 1885, Michelson collaborated with Edward Morley, spending considerable time and money to repeat the Fizeau experiment on Fresnel's drag coefficient (finished in 1886)', [1] and to repeat the Michelson experiment (finished in 1887). [2]