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  2. Bromocyclopentane - Wikipedia

    en.wikipedia.org/wiki/Bromocyclopentane

    Bromocyclopentane is a derivative of cyclopentane, an alkyl halide with the chemical formula C 5 H 9 Br. It is a colorless to light yellow liquid at standard temperature and pressure . Uses

  3. Bromopentane - Wikipedia

    en.wikipedia.org/wiki/Bromopentane

    They have the formula C 5 H 12–n Br n, where n = 1–12 is the number of bromine atoms. They are colorless liquids. They are colorless liquids. Monobromopentane

  4. 2-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/2-Bromopentane

    2-Bromopentane is a bromoalkane and isomer of bromopentane. It is a colorless liquid. 2-Bromopentane is chiral and thus can be obtained as either of two stereoisomers designated as ( R )-2-bromopentane and ( S )-2-bromopentane, or as a racemic 1:1 mixture of the two enantiomers .

  5. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    The two reactions are named according tho their rate law, with S N 1 having a first-order rate law, and S N 2 having a second-order. [2] S N 1 reaction mechanism occurring through two steps. The S N 1 mechanism has two steps. In the first step, the leaving group departs, forming a carbocation (C +). In the second step, the nucleophilic reagent ...

  6. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    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-determining step is unimolecular .

  7. SNi - Wikipedia

    en.wikipedia.org/wiki/SNi

    With standard S N 1 reaction conditions the reaction outcome is retention via a competing S N i mechanism and not racemization and with pyridine added the result is again inversion. [5] [3] S N i reaction mechanism Sn1 occurs in tertiary carbon while Sn2 occurs in primary carbon

  8. Finkelstein reaction - Wikipedia

    en.wikipedia.org/wiki/Finkelstein_reaction

    The Finkelstein reaction, named after the German chemist Hans Finkelstein, [1] is a type of S N 2 reaction (substitution nucleophilic bimolecular reaction) that involves the exchange of one halogen atom for another.

  9. Associative substitution - Wikipedia

    en.wikipedia.org/wiki/Associative_substitution

    V = z 1 z 2 e 2 /4πaε Where z is the charge number of each species and ε is the vacuum permittivity . A typical value for K E is 0.0202 dm 3 mol −1 for neutral particles at a distance of 200 pm. [ 9 ] The result of the rate law is that at high concentrations of Y, the rate approximates k[M] tot while at low concentrations the result is kK ...