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  2. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    Ethylamine, also known as ethanamine, is an organic compound with the formula CH 3 CH 2 NH 2. This colourless gas has a strong ammonia-like odor. It condenses just below room temperature to a liquid miscible with virtually all solvents. It is a nucleophilic base, as is typical for amines. Ethylamine is widely used in chemical industry and ...

  3. Ethyleneamine - Wikipedia

    en.wikipedia.org/wiki/Ethyleneamine

    In all these examples, stoichiometric base is needed to convert the amine hydrochloride to free amines. In the monoethanolamine route, monoethanolamine reacts with ammonia, catalyzed by transition metal catalysts. This process is reported to generate more cyclic compounds than the ethylene dichloride route. [2]

  4. Hydroamination - Wikipedia

    en.wikipedia.org/wiki/Hydroamination

    Strong bases catalyze hydroamination, an example being the ethylation of piperidine using ethene: [27] Hydroamination of ethene with piperidine proceeds with no transition metal catalyst, but requires a strong base. Such base catalyzed reactions proceed well with ethene but higher alkenes are less reactive.

  5. Biological basis of personality - Wikipedia

    en.wikipedia.org/wiki/Biological_basis_of...

    The biological basis of personality is a collection of brain systems and mechanisms that underlie human personality. Human neurobiology, especially as it relates to complex traits and behaviors, is not well understood, but research into the neuroanatomical and functional underpinnings of personality are an active field of research.

  6. Ethylenediamine - Wikipedia

    en.wikipedia.org/wiki/Ethylenediamine

    Ethylenediamine (abbreviated as en when a ligand) is the organic compound with the formula C 2 H 4 (NH 2) 2.This colorless liquid with an ammonia-like odor is a basic amine.It is a widely used building block in chemical synthesis, with approximately 500,000 tonnes produced in 1998. [6]

  7. N,N-Diisopropylethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-Diisopropylethylamine

    DIPEA is a sterically hindered organic base that is commonly employed as a proton scavenger. Thus, like 2,2,6,6-tetramethylpiperidine and triethylamine, DIPEA is a good base but a poor nucleophile, DIPEA has low solubility in water, which makes it very easily recovered in commercial processes, a combination of properties that makes it a useful organic reagent.

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  9. Enthalpy of neutralization - Wikipedia

    en.wikipedia.org/wiki/Enthalpy_of_neutralization

    In chemistry and thermodynamics, the enthalpy of neutralization (ΔH n) is the change in enthalpy that occurs when one equivalent of an acid and a base undergo a neutralization reaction to form water and a salt. It is a special case of the enthalpy of reaction. It is defined as the energy released with the formation of 1 mole of water.