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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. 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 ...

  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. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    An example of a reaction proceeding in a S N 1 fashion is the synthesis of 2,5-dichloro-2,5-dimethylhexane from the corresponding diol with concentrated hydrochloric acid: [8] As the alpha and beta substitutions increase with respect to leaving groups, the reaction is diverted from S N 2 to S N 1.

  6. 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

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  9. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    What distinguishes S N 2 from the other major type of nucleophilic substitution, the S N 1 reaction, is that the displacement of the leaving group, which is the rate-determining step, is separate from the nucleophilic attack in S N 1. The S N 2 reaction can be considered as an organic-chemistry analogue of the associative substitution from the ...

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