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  2. n-Butylamine - Wikipedia

    en.wikipedia.org/wiki/N-Butylamine

    n-Butylamine is an organic compound (specifically, an amine) with the formula CH 3 (CH 2) 3 NH 2. This colourless liquid is one of the four isomeric amines of butane, the others being sec-butylamine, tert-butylamine, and isobutylamine. It is a liquid having the fishy, ammonia-like odor common to amines. The liquid acquires a yellow color upon ...

  3. C4H11N - Wikipedia

    en.wikipedia.org/wiki/C4H11N

    The molecular formula C 4 H 11 N may refer to: n-Butylamine; sec-Butylamine; tert-Butylamine; Diethylamine; N,N-Dimethylethylamine; Isobutylamine

  4. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    In terms of Lewis structures, formal charge is used in the description, comparison, and assessment of likely topological and resonance structures [7] by determining the apparent electronic charge of each atom within, based upon its electron dot structure, assuming exclusive covalency or non-polar bonding.

  5. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    Polar molecules must contain one or more polar bonds due to a difference in electronegativity between the bonded atoms. Molecules containing polar bonds have no molecular polarity if the bond dipoles cancel each other out by symmetry. Polar molecules interact through dipole-dipole intermolecular forces and hydrogen bonds.

  6. Butylamine - Wikipedia

    en.wikipedia.org/wiki/Butylamine

    tert-Butylamine; Isobutylamine This page was last edited on 23 February 2023, at 19:01 (UTC). Text is available under the Creative Commons Attribution-ShareAlike ...

  7. 1-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/1-Bromobutane

    As a primary haloalkane, it is prone to S N 2 type reactions. It is commonly used as an alkylating agent. When combined with magnesium metal in dry ether, it gives the corresponding Grignard reagent. Such reagents are used to attach butyl groups to various substrates. 1-Bromobutane is the precursor to n-butyllithium: [4] 2 Li + C 4 H 9 X → C ...

  8. Butyl group - Wikipedia

    en.wikipedia.org/wiki/Butyl_group

    In organic chemistry, butyl is a four-carbon alkyl radical or substituent group with general chemical formula −C 4 H 9, derived from either of the two isomers (n-butane and isobutane) of butane. The isomer n -butane can connect in two ways, giving rise to two "-butyl" groups:

  9. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    Like other simple aliphatic amines, ethylamine is a weak base: the pK a of [CH 3 CH 2 NH 3] + has been determined to be 10.8 [8] [9]. Ethylamine undergoes the reactions anticipated for a primary alkyl amine, such as acylation and protonation.