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  2. Hemiacetal - Wikipedia

    en.wikipedia.org/wiki/Hemiacetal

    In organic chemistry, a hemiacetal is a functional group the general formula R 1 R 2 C(OH)OR, where R 1, R 2 is a hydrogen atom or an organic substituent. They generally result from the nucleophilic addition of an alcohol (a compound with at least one hydroxy group ) to an aldehyde ( R−CH=O ) or a ketone ( R 2 C=O ) under acidic conditions.

  3. Carbohydrate acetalisation - Wikipedia

    en.wikipedia.org/wiki/Carbohydrate_acetalisation

    The latter reagent in itself is an acetal and therefore the reaction is actually a cross-acetalisation. Kinetic reaction control results from 2-methoxypropene as the reagent. D-ribose in itself is a hemiacetal and in equilibrium with the pyranose 3. In aqueous solution ribose is 75% pyranose and 25% furanose and a different acetal 4 is formed.

  4. Tetrahedral carbonyl addition compound - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_carbonyl...

    Acid catalyzed acetal formation from the corresponding hemiacetal. Acetals, as already pointed out, are stable tetrahedral intermediates so they can be used as protective groups in organic synthesis. Acetals are stable under basic conditions, so they can be used to protect ketones from a base. The acetal group is hydrolyzed under acidic conditions.

  5. Acetal - Wikipedia

    en.wikipedia.org/wiki/Acetal

    Used in a more general sense, the term X,Y-acetal also refers to any functional group that consists of a carbon bearing two heteroatoms X and Y. For example, N , O -acetal refers to compounds of type R 1 R 2 C(OR)(NR' 2 ) (R,R' ≠ H) also known as a hemiaminal ether or Aminal , a.k.a. aminoacetal.

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