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  2. Hemiacetal - Wikipedia

    en.wikipedia.org/wiki/Hemiacetal

    According to the IUPAC definition of a hemiacetal, the R 1 and R 2 groups may or may not be hydrogen. In a hemiketal, both of these R-groups must not be hydrogen. Thus, hemiketals are regarded as a subclass of hemiacetals. [1] The prefix hemi, meaning half, refers to the one alcohol added to the carbonyl group.

  3. Acetal - Wikipedia

    en.wikipedia.org/wiki/Acetal

    Generic structure of acetals. In organic chemistry, an acetal is a functional group with the connectivity R 2 C(OR') 2. Here, the R groups can be organic fragments (a carbon atom, with arbitrary other atoms attached to that) or hydrogen, while the R' groups must be organic fragments not hydrogen. The two R' groups can be equivalent to each ...

  4. Hemithioacetal - Wikipedia

    en.wikipedia.org/wiki/Hemithioacetal

    Hemithioacetal functional group. In organic chemistry, hemithioacetals (or thiohemiacetals) are organosulfur compounds with the general formula R−CH(−OH)−SR’.They are the sulfur analogues of the acetals, R−CH(−OH)−OR’, with an oxygen atom replaced by sulfur (as implied by the thio-prefix).

  5. Hemiaminal - Wikipedia

    en.wikipedia.org/wiki/Hemiaminal

    Methanolamine, a simple hemiaminal. The adducts formed by the addition of ammonia to aldehydes have long been studied. [3] Compounds containing both a primary amino group and a hydroxyl group bonded to the same carbon atom are rarely stable ("The hemiaminal [derived from primary amines] is, except in very special cases... not observed"), [4] as they tend to dehydrate to form imines which ...

  6. IUPAC numerical multiplier - Wikipedia

    en.wikipedia.org/wiki/IUPAC_numerical_multiplier

    The IUPAC numerical multiplier is a system of prefixes used in chemistry to indicate the number of atoms or groups in a molecule.

  7. Spiro compound - Wikipedia

    en.wikipedia.org/wiki/Spiro_compound

    A spiro compound, or spirane, from the Latin spīra, meaning a twist or coil, [22] [5]: 1138 [23] is a chemical compound, typically an organic compound, that presents a twisted structure of two or more rings (a ring system), in which 2 or 3 rings are linked together by one common atom, [2]: SP-0

  8. Pyranose - Wikipedia

    en.wikipedia.org/wiki/Pyranose

    The pyranose ring is formed by the reaction of the hydroxyl group on carbon 5 (C-5) of a sugar with the aldehyde at carbon 1. This forms an intramolecular hemiacetal.If reaction is between the C-4 hydroxyl and the aldehyde, a furanose is formed instead. [1]

  9. Acetyl group - Wikipedia

    en.wikipedia.org/wiki/Acetyl_group

    In organic chemistry, an acetyl group is a functional group denoted by the chemical formula −COCH 3 and the structure −C(=O)−CH 3.It is sometimes represented by the symbol Ac [5] [6] (not to be confused with the element actinium).