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  2. Sodium hydride - Wikipedia

    en.wikipedia.org/wiki/Sodium_hydride

    Sodium hydride is the chemical compound with the empirical formula Na H.This alkali metal hydride is primarily used as a strong yet combustible base in organic synthesis.NaH is a saline (salt-like) hydride, composed of Na + and H − ions, in contrast to molecular hydrides such as borane, silane, germane, ammonia, and methane.

  3. Krische allylation - Wikipedia

    en.wikipedia.org/wiki/Krische_allylation

    A remarkable feature of these reactions is the ability to conduct carbonyl allylation from the alcohol oxidation state. Due to a kinetic preference for primary alcohol dehydrogenation, diols containing both primary and secondary alcohols undergo site-selective carbonyl allylation at the primary alcohol without the need for protecting groups. [18]

  4. Alcohol (chemistry) - Wikipedia

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

    The term alcohol originally referred to the primary alcohol ethanol (ethyl alcohol), which is used as a drug and is the main alcohol present in alcoholic drinks. The suffix -ol appears in the International Union of Pure and Applied Chemistry (IUPAC) chemical name of all substances where the hydroxyl group is the functional group with the ...

  5. Alcohol oxidation - Wikipedia

    en.wikipedia.org/wiki/Alcohol_oxidation

    Alcohol oxidation is a collection of oxidation reactions in organic chemistry that convert alcohols to aldehydes, ketones, carboxylic acids, and esters. The reaction mainly applies to primary and secondary alcohols. Secondary alcohols form ketones, while primary alcohols form aldehydes or carboxylic acids. [1] A variety of oxidants can be used.

  6. 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.

  7. Nucleophilic addition - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_addition

    an alcohol in acetalisation to an acetal; a hydride in reduction to an alcohol; an amine with formaldehyde and a carbonyl compound in the Mannich reaction; an enolate ion in an aldol reaction or Baylis–Hillman reaction; an organometallic nucleophile in the Grignard reaction or the related Barbier reaction or a Reformatskii reaction

  8. Drunk People Spilled These 40 Secrets, Regret It Greatly - AOL

    www.aol.com/lifestyle/41-people-reveal-drunken...

    Image credits: Scry1Draw1 Alcohol has long been seen as a "truth serum," encouraging hours of "brutal honesty" that you may, or may not, live to regret. There's an old Latin saying that goes "In ...

  9. Alcohol flush reaction - Wikipedia

    en.wikipedia.org/wiki/Alcohol_flush_reaction

    The reaction is the result of an accumulation of acetaldehyde, a metabolic byproduct of the catabolic metabolism of alcohol, and is caused by an aldehyde dehydrogenase 2 deficiency. [ 4 ] This syndrome has been associated with lower than average rates of alcoholism, possibly due to its association with adverse effects after drinking alcohol. [ 5 ]