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  2. Formaldehyde - Wikipedia

    en.wikipedia.org/wiki/Formaldehyde

    Formaldehyde is readily oxidized by atmospheric oxygen into formic acid. For this reason, commercial formaldehyde is typically contaminated with formic acid. Formaldehyde can be hydrogenated into methanol. In the Cannizzaro reaction, formaldehyde and base react to produce formic acid and methanol, a disproportionation reaction.

  3. Mannich reaction - Wikipedia

    en.wikipedia.org/wiki/Mannich_reaction

    The Schiff base is an electrophile which reacts in a second step in an electrophilic addition with an enol formed from a carbonyl compound containing an acidic alpha-proton. The Mannich reaction is a condensation reaction. [4]: 140 In the Mannich reaction, primary or secondary amines or ammonia react with formaldehyde to form a Schiff base ...

  4. Eschweiler–Clarke reaction - Wikipedia

    en.wikipedia.org/wiki/Eschweiler–Clarke_reaction

    The reaction is generally performed in an aqueous solution at close to boiling. The first methylation of the amine begins with imine formation with formaldehyde. The formic acid acts as a source of hydride and reduces the imine to a secondary amine. Loss of carbon dioxide gas renders the reaction irreversible. Despite being more hindered, the ...

  5. Formox process - Wikipedia

    en.wikipedia.org/wiki/Formox_process

    On it, two chemical reactions simultaneously produce formaldehyde: the one shown above, and the dehydrogenation reaction: CH 3 OH → H 2 CO + H 2. Further oxidation of the formaldehyde product during its production usually gives formic acid that is found in formaldehyde solution, found in parts per million values.

  6. Phenol formaldehyde resin - Wikipedia

    en.wikipedia.org/wiki/Phenol_formaldehyde_resin

    Phenol-formaldehyde resins, as a group, are formed by a step-growth polymerization reaction that can be either acid- or base-catalysed.Since formaldehyde exists predominantly in solution as a dynamic equilibrium of methylene glycol oligomers, the concentration of the reactive form of formaldehyde depends on temperature and pH.

  7. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.

  8. Formic acid - Wikipedia

    en.wikipedia.org/wiki/Formic_acid

    Formic acid readily decomposes by dehydration in the presence of concentrated sulfuric acid to form carbon monoxide and water: HCO 2 H → H 2 O + CO. Treatment of formic acid with sulfuric acid is a convenient laboratory source of CO. [15] [16] In the presence of platinum, it decomposes with a release of hydrogen and carbon dioxide. HCO 2 H ...

  9. Formose reaction - Wikipedia

    en.wikipedia.org/wiki/Formose_reaction

    The formose reaction is of importance to the question of the origin of life, as it leads from simple formaldehyde to complex sugars like ribose, a building block of RNA.In one experiment simulating early Earth conditions, pentoses formed from mixtures of formaldehyde, glyceraldehyde, and borate minerals such as colemanite (Ca 2 B 6 O 11 5H 2 O) or kernite (Na 2 B 4 O 7). [6]