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  2. 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:

  3. Glycolonitrile - Wikipedia

    en.wikipedia.org/wiki/Glycolonitrile

    Glycolonitrile, also called hydroxyacetonitrile or formaldehyde cyanohydrin, is the organic compound with the formula HOCH 2 CN. It is the simplest cyanohydrin and it is derived from formaldehyde . [ 3 ]

  4. 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 ...

  5. Category:Cyanohydrins - Wikipedia

    en.wikipedia.org/wiki/Category:Cyanohydrins

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  6. 7 Alternatives to Chemotherapy for Lymphoma in Dogs - AOL

    www.aol.com/7-alternatives-chemotherapy-lymphoma...

    1. Ketogenic Diet. Cancer cells rely on glucose for energy to grow. The ketogenic diet is a way to provide an alternative energy source to normal cells in the dog's body while starving the cancer ...

  7. Alpha hydroxycarboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Alpha_hydroxycarboxylic_acid

    Another synthetic pathway for α-hydroxy acids involves the addition of hydrogen cyanide to ketones or aldehydes, followed by the acidic hydrolysis of the cyanohydrin intermediate. [14] R−CHO + HCN → R−CH(OH)CN R−CH(OH)CN + 2H 2 O → R−CH(OH)CO 2 H + NH 3

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