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  2. Fluorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Fluorobenzaldehyde

    Fluorobenzaldehyde can be used as a synthetic intermediate because the fluorine can be replaced via oxidation reaction. [1] Due to the aldehyde group, the fluorobenzaldehydes can be used to make a variety of schiff base compounds through a condensation reaction , some of which have antimicrobial properties.

  3. 2-Chloro-6-fluorobenzaldehyde - Wikipedia

    en.wikipedia.org/wiki/2-Chloro-6-fluorobenzaldehyde

    2-Chloro-6-fluorobenzaldehyde is prepared by oxidation of 2-chloro-6-fluorotolulene by chromyl chloride. [3] It reacts with sodium hydroxide to give a mixture of 2-chloro-6-fluorobenzene and 6-chlorosalicaldehyde. [4] 2-Chloro-6-fluorobenzaldehyde is used in the production of the antiseptics dicloxacillin and flucloxacillin.

  4. Metamerism (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Metamerism_(Chemistry)

    The isomers which have been cited as examples of metamers in chemical literature consist primarily of ethers; [3] but this could by the same reasoning be extended to thioethers, secondary as well as tertiary amines, esters, secondary as well as tertiary amides, (mixed) acid anhydrides etc. Metamers in organic chemistry

  5. E–Z notation - Wikipedia

    en.wikipedia.org/wiki/E–Z_notation

    E–Z configuration, or the E–Z convention, is the IUPAC preferred method of describing the absolute stereochemistry of double bonds in organic chemistry.It is an extension of cis–trans isomer notation (which only describes relative stereochemistry) that can be used to describe double bonds having two, three or four substituents.

  6. Isomerization - Wikipedia

    en.wikipedia.org/wiki/Isomerization

    The compound with the formula (C 5 H 5) 2 Fe 2 (CO) 4 exists as three isomers in solution. In one isomer the CO ligands are terminal. When a pair of CO are bridging, cis and trans isomers are possible depending on the location of the C 5 H 5 groups. [7] Another example in organometallic chemistry is the linkage isomerization of ...

  7. Valence isomer - Wikipedia

    en.wikipedia.org/wiki/Valence_isomer

    The valence isomers are not restricted to isomers of benzene. Valence isomers are also seen in the series (CH) 8. Due to the larger number of units, the number of possible valence isomers is also greater and at least 21: Valence isomers of cyclooctatetraene

  8. Pentafluorobenzene - Wikipedia

    en.wikipedia.org/wiki/Pentafluorobenzene

    Pentafluorobenzene is an organofluoride compound with the molecular formula C 6 HF 5. [1] The compound consists of a benzene ring substituted with five fluorine atoms. [2] The substance is a colorless liquid with a boiling point similar to that of benzene.

  9. Cycloisomerization - Wikipedia

    en.wikipedia.org/wiki/Cycloisomerization

    A rather intuitive route to cyclic isomers is the intramolecular conjugate addition to α,β–unsaturated carbonyls (intramolecular Michael addition or IMA). Competent Michael acceptors include conjugated enones, enals or nitroalkene derivatives and examples of other acceptors are sparse. [3]