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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. SNi - Wikipedia

    en.wikipedia.org/wiki/SNi

    S N i reaction mechanism Sn1 occurs in tertiary carbon while Sn2 occurs in primary carbon. See also. Nucleophilic acyl substitution; References. This page was last ...

  4. 2-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/2-Bromopentane

    Van der Waals space filling structure of (R)-2-bromopentane (R)-2-bromopentane. ... Chemical formula. C 5 H 11 Br: Molar mass: 151.047 g·mol −1 Appearance ...

  5. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    The carbocation intermediate formed in the reaction's rate determining step (RDS) is an sp 2 hybridized carbon with trigonal planar molecular geometry. This allows two different ways for the nucleophilic attack, one on either side of the planar molecule.

  6. Hammett equation - Wikipedia

    en.wikipedia.org/wiki/Hammett_equation

    For example, the substituent may determine the mechanism to be an SN1 type reaction over a SN2 type reaction, in which case the resulting Hammett plot will indicate a rate acceleration due to an EDG, thus elucidating the mechanism of the reaction. Another deviation from the regular Hammett equation is explained by the charge of nucleophile.

  7. 1-Lysophosphatidylcholine - Wikipedia

    en.wikipedia.org/wiki/1-Lysophosphatidylcholine

    General chemical structure of 1-lyso-phosphatidylcholines, where R is a variable fatty acyl group. 1-Lysophosphatidylcholines (or 1-lysoPC) are a class of phospholipids that are intermediates in the metabolism of lipids. They result from the hydrolysis of an acyl group from the sn-1 position of phosphatidylcholine.

  8. Hammond's postulate - Wikipedia

    en.wikipedia.org/wiki/Hammond's_postulate

    Hammond's postulate (or alternatively the Hammond–Leffler postulate), is a hypothesis in physical organic chemistry which describes the geometric structure of the transition state in an organic chemical reaction. [1] First proposed by George Hammond in 1955, the postulate states that: [2]

  9. Arrow pushing - Wikipedia

    en.wikipedia.org/wiki/Arrow_pushing

    Arrow pushing or electron pushing is a technique used to describe the progression of organic chemistry reaction mechanisms. [1] It was first developed by Sir Robert Robinson.In using arrow pushing, "curved arrows" or "curly arrows" are drawn on the structural formulae of reactants in a chemical equation to show the reaction mechanism.