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  2. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehydes have properties that are diverse and that depend on the remainder of the molecule. Smaller aldehydes such as formaldehyde and acetaldehyde are soluble in water, and the volatile aldehydes have pungent odors. Aldehydes can be identified by spectroscopic methods. Using IR spectroscopy, they display a strong ν CO band near 1700 cm −1.

  3. Properties of water - Wikipedia

    en.wikipedia.org/wiki/Properties_of_water

    Although hydrogen bonding is a relatively weak attraction compared to the covalent bonds within the water molecule itself, it is responsible for several of the water's physical properties. These properties include its relatively high melting and boiling point temperatures: more energy is required to break the hydrogen bonds between water molecules.

  4. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    Ketones are trigonal planar around the ketonic carbon, with C–C–O and C–C–C bond angles of approximately 120°. Ketones differ from aldehydes in that the carbonyl group (C=O) is bonded to two carbons within a carbon skeleton. In aldehydes, the carbonyl is bonded to one carbon and one hydrogen and are located at the ends of carbon chains.

  5. Aldol condensation - Wikipedia

    en.wikipedia.org/wiki/Aldol_condensation

    An aldol condensation is a condensation reaction in organic chemistry in which two carbonyl moieties (of aldehydes or ketones) react to form a β-hydroxyaldehyde or β-hydroxyketone (an aldol reaction), and this is then followed by dehydration to give a conjugated enone.

  6. Butyraldehyde - Wikipedia

    en.wikipedia.org/wiki/Butyraldehyde

    The dominant technology involves the use of rhodium catalysts derived from the water-soluble ligand tppts. An aqueous solution of the rhodium catalyst converts the propylene to the aldehyde, which forms a lighter (less dense) immiscible phase. About 6 billion kilograms are produced annually in this manner.

  7. Oxime - Wikipedia

    en.wikipedia.org/wiki/Oxime

    The condensation of aldehydes with hydroxylamine gives aldoximes, and ketoximes are produced from ketones and hydroxylamine. In general, oximes exist as colorless crystals or as thick liquids and are poorly soluble in water. Therefore, oxime formation can be used for the identification of ketone or aldehyde functional groups.

  8. Water - Wikipedia

    en.wikipedia.org/wiki/Water

    Water (data page) – Chemical data page for water is a collection of the chemical and physical properties of water. Aquaphobia – Persistent and abnormal fear of water; Blue roof – Roof of a building that is designed to provide temporary water storage; Catchwater – Runoff catching or channeling device; Human right to water and sanitation

  9. Hemiacetal - Wikipedia

    en.wikipedia.org/wiki/Hemiacetal

    Hemiacetals form in the reaction between alcohols and aldehydes or ketones. Using an acid catalyst, the reaction proceeds via nucleophilic attack of the carbonyl group by the alcohol. [4] A subsequent nucleophilic attack of the hemiacetal by the alcohol results in an acetal. [2] Solutions of simple aldehydes in alcohols mainly consist of the ...