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  2. Hydrocyanation - Wikipedia

    en.wikipedia.org/wiki/Hydrocyanation

    In transhydrocyanation, an equivalent of HCN is transferred from a cyanohydrin, e.g. acetone cyanohydrin, to another HCN acceptor. The transfer is an equilibrium process, initiated by base. The reaction can be driven by trapping reactions or by the use of a superior HCN acceptor, such as an aldehyde. [6]

  3. Cyanohydrin reaction - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin_reaction

    In organic chemistry, a cyanohydrin reaction is an organic reaction in which an aldehyde (−CH=O) or ketone (>C=O) reacts with a cyanide anion ...

  4. Cyanohydrin - Wikipedia

    en.wikipedia.org/wiki/Cyanohydrin

    In the laboratory, this liquid serves as a source of HCN, which is inconveniently volatile. [4] Thus, acetone cyanohydrin can be used for the preparation of other cyanohydrins, for the transformation of HCN to Michael acceptors, and for the formylation of arenes. Treatment of this cyanohydrin with lithium hydride affords anhydrous lithium cyanide:

  5. Acetone cyanohydrin - Wikipedia

    en.wikipedia.org/wiki/Acetone_cyanohydrin

    [7] It is used as a surrogate in place of HCN, as illustrated by its use as a precursor to lithium cyanide: [8] (CH 3) 2 C(OH)CN + LiH → (CH 3) 2 CO + LiCN + H 2. In transhydrocyanation, an equivalent of HCN is transferred from acetone cyanohydrin to another acceptor, with acetone as byproduct. The transfer is an equilibrium process ...

  6. Fischer oxazole synthesis - Wikipedia

    en.wikipedia.org/wiki/Fischer_oxazole_synthesis

    [1] The cyanohydrins and aldehydes used for the synthesis are usually aromatic, however there have been instances where aliphatic compounds have been used. The first step of the mechanism is the addition of gaseous HCl to the cyanohydrin 1. The cyanohydrin abstracts the hydrogen from HCl while the chloride ion attacks the carbon in the cyano group.

  7. Alpha hydroxycarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Alpha_hydroxycarboxylic_acid

    This structural aspect distinguishes them from beta hydroxy acids, where the functional groups are separated by two carbon atoms. [1] Notable AHAs include glycolic acid, lactic acid, mandelic acid, and citric acid. α-Hydroxy acids are stronger acids compared to their non-alpha hydroxy counterparts, a property enhanced by internal hydrogen bonding.

  8. Small business owners must report by end of the year to avoid ...

    www.aol.com/small-business-owners-must-report...

    Small business owners face severe penalties if they don't report to the federal government by year's end. Thousands of businesses may not realize they are subject to a new reporting process ...

  9. Dosage Index - Wikipedia

    en.wikipedia.org/wiki/Dosage_Index

    The Dosage Index is a mathematical figure used by breeders of Thoroughbred race horses, and sometimes by bettors handicapping horse races, to quantify a horse's ability, or inability, to negotiate the various distances at which horse races are run. It is calculated based on an analysis of the horse's pedigree.

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