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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. 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 ...

  4. 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.

  5. 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

  6. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    For example, the three isomers of xylene CH 3 C 6 H 4 CH 3, commonly the ortho-, meta-, and para-forms, are 1,2-dimethylbenzene, 1,3-dimethylbenzene, and 1,4-dimethylbenzene. The cyclic structures can also be treated as functional groups themselves, in which case they take the prefix "cyclo alkyl -" (e.g. "cyclohexyl-") or for benzene, "phenyl-".

  7. Bredt's rule - Wikipedia

    en.wikipedia.org/wiki/Bredt's_rule

    For bicyclic systems examples now indicate a limit of S ≥ 7, [6] with several such compounds having been prepared. [11] Bridgehead double bonds can be found in some natural products. [12] Bredt's rule can predict the viability of competing elimination reactions in a bridged system.

  8. Alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Alkylbenzene

    Alkylbenzene isomers can be differentiated by observing the position of alkyl substituents on the benzene ring using chemical ionization-proton exchange mass spectrometry. Conventional GC-MS yields limited results because the isomers have identical molecular weight and substituents.

  9. Photoisomerization - Wikipedia

    en.wikipedia.org/wiki/Photoisomerization

    One case is the conversion of the colorless cis-bis(triphenylphosphine)platinum chloride to the yellow trans isomer. Photoisomerization of PtCl 2 (PPh 3 ) 2 Some coordination complexes undergo change in their spin state upon illumination, i.e. these are photosensitive spin crossover complexes.

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