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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. [2] [3]

  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. List of chemistry mnemonics - Wikipedia

    en.wikipedia.org/wiki/List_of_chemistry_mnemonics

    A mnemonic is a memory aid used to improve long-term memory and make the process of consolidation easier. Many chemistry aspects, rules, names of compounds, sequences of elements, their reactivity, etc., can be easily and efficiently memorized with the help of mnemonics.

  5. 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 ...

  6. 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

  7. Fluorous chemistry - Wikipedia

    en.wikipedia.org/wiki/Fluorous_chemistry

    The fluorous domain is often a substituent intended to confer solubility in the fluorocarbon medium. Such perfluorosubstituents are often introduced in what are called ponytails. Typical fluorous ponytails have the formula CF 3 (CF 2) n (CH 2) m - where n is about 10 and m is about 3. [1]

  8. Category:Fluorobenzene derivatives - Wikipedia

    en.wikipedia.org/wiki/Category:Fluorobenzene...

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  9. Valence isomer - Wikipedia

    en.wikipedia.org/wiki/Valence_isomer

    Tricyclo[4,2,0,0 2,5]octa-3,7-diene. The dimer of cyclobutadiene occurs as a cis isomer and a trans isomer. Both isomers convert to COT (symmetry forbidden hence stable) with a half-life of 20 minutes at 140 °C [ 10 ]