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  2. Amine alkylation - Wikipedia

    en.wikipedia.org/wiki/Amine_alkylation

    Amine alkylation (amino-dehalogenation) is a type of organic reaction between an alkyl halide and ammonia or an amine. [1] The reaction is called nucleophilic aliphatic substitution (of the halide), and the reaction product is a higher substituted amine. The method is widely used in the laboratory, but less so industrially, where alcohols are ...

  3. Gabriel synthesis - Wikipedia

    en.wikipedia.org/wiki/Gabriel_synthesis

    Upon workup by acidic hydrolysis the primary amine is liberated as the amine salt. [11] Alternatively the workup may be via the Ing–Manske procedure, involving reaction with hydrazine. This method produces a precipitate of phthalhydrazide (C 6 H 4 (CO) 2 N 2 H 2) along with the primary amine: C 6 H 4 (CO) 2 NR + N 2 H 4 → C 6 H 4 (CO) 2 N 2 ...

  4. Ammonolysis - Wikipedia

    en.wikipedia.org/wiki/Ammonolysis

    In chemistry, ammonolysis (/am·mo·nol·y·sis/) is the process of splitting ammonia into + +. [1] Ammonolysis reactions can be conducted with organic compounds to produce amines (molecules containing a nitrogen atom with a lone pair, :N), [2] or with inorganic compounds to produce nitrides.

  5. Haloalkane - Wikipedia

    en.wikipedia.org/wiki/Haloalkane

    Tetrafluoroethane (a haloalkane) is a colorless liquid that boils well below room temperature (as seen here) and can be extracted from common canned air canisters by simply inverting them during use. The haloalkanes (also known as halogenoalkanes or alkyl halides) are alkanes containing one or more halogen substituents. [1]

  6. Dehydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehydrohalogenation

    In general, the reaction of a haloalkane with potassium hydroxide can compete with an S N 2 nucleophilic substitution reaction by OH − a strong, unhindered nucleophile. Alcohols are however generally minor products. Dehydrohalogenations often employ strong bases such as potassium tert-butoxide (K + [CH 3] 3 CO −).

  7. Baylis–Hillman reaction - Wikipedia

    en.wikipedia.org/wiki/Baylis–Hillman_reaction

    The MBH reaction is extremely general. In most cases the electrophile is an aldehyde, ketone (but see below), or imine (latterly the aza-Baylis–Hillman reaction); but reports indicate that allyl halides, alkyl halides, and epoxides are also possible.

  8. Mind-altering ketamine becomes latest pain treatment ... - AOL

    www.aol.com/news/mind-altering-ketamine-becomes...

    As U.S. doctors scale back their use of opioid painkillers, a new option for hard-to-treat pain is taking root: ketamine, the decades-old surgical drug that is now a trendy psychedelic therapy.

  9. Functional group - Wikipedia

    en.wikipedia.org/wiki/Functional_group

    Haloalkanes are a class of molecule that is defined by a carbon–halogen bond. This bond can be relatively weak (in the case of an iodoalkane) or quite stable (as in the case of a fluoroalkane). In general, with the exception of fluorinated compounds, haloalkanes readily undergo nucleophilic substitution reactions or elimination reactions. The ...