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  2. 2-Bromobutane - Wikipedia

    en.wikipedia.org/wiki/2-Bromobutane

    2-Bromobutane is an isomer of 1-bromobutane. Both compounds share the molecular formula C 4 H 9 Br. 2-Bromobutane is also known as sec-butyl bromide or methylethylbromomethane. Because it contains bromine, a halogen, it is part of a larger class of compounds known as alkyl halides. It is a colorless liquid with a pleasant odor.

  3. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    The leaving group is denoted "X", and the nucleophile is denoted "Nu–H". The unimolecular nucleophilic substitution ( S N 1 ) reaction is a substitution reaction in organic chemistry . The Hughes-Ingold symbol of the mechanism expresses two properties—"S N " stands for " nucleophilic substitution ", and the "1" says that the rate ...

  4. Solvolysis - Wikipedia

    en.wikipedia.org/wiki/Solvolysis

    In chemistry, solvolysis is a type of nucleophilic substitution (S N 1/S N 2) or elimination where the nucleophile is a solvent molecule. [1] Characteristic of S N 1 reactions, solvolysis of a chiral reactant affords the racemate.

  5. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    An example of a substitution reaction taking place by a so-called borderline mechanism as originally studied by Hughes and Ingold [6] is the reaction of 1-phenylethyl chloride with sodium methoxide in methanol. The reaction rate is found to the sum of S N 1 and S N 2 components with 61% (3,5 M, 70 °C) taking place by the latter.

  6. C4H9Br - Wikipedia

    en.wikipedia.org/wiki/C4H9Br

    The molecular formula C 4 H 9 Br, (molar mass: 137.02 g/mol, exact mass: 135.9888 u) may refer to: 1-Bromobutane; 2-Bromobutane; tert-Butyl bromide;

  7. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    This results in S N 1 reactions usually occurring on atoms with at least two carbons bonded to them. [2] A more detailed explanation of this can be found in the main SN1 reaction page. S N 2 reaction mechanism. The S N 2 mechanism has just one step. The attack of the reagent and the expulsion of the leaving group happen simultaneously.

  8. Bromobenzene - Wikipedia

    en.wikipedia.org/wiki/Bromobenzene

    This reagent can be used, e.g. in the reaction with carbon dioxide to prepare benzoic acid. [4] Other methods involve palladium-catalyzed coupling reactions , such as the Suzuki reaction . Bromobenzene is used as a precursor in the manufacture of phencyclidine .

  9. Bromobutane - Wikipedia

    en.wikipedia.org/wiki/Bromobutane

    Bromobutane (molecular formula: C 4 H 9 Br, molar mass: 137.02 g/mol) may refer to either of two chemical compounds: 1-Bromobutane (n-butyl bromide)