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  2. tert-Butyl bromide - Wikipedia

    en.wikipedia.org/wiki/Tert-butyl_bromide

    tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert-butyl group attached to a bromide substituent. This organobromine compound is used as a standard reagent in synthetic organic chemistry. It is a colorless liquid.

  3. C4H9Br - Wikipedia

    en.wikipedia.org/wiki/C4H9Br

    5 languages. العربية ... 1-bromo-2-methylpropane This page was last edited on 16 August 2021, at 07:47 (UTC). Text is available under the Creative Commons ...

  4. 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

  5. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    The stability of a carbocation (C +) depends on how many other carbon atoms are bonded to it. 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 ...

  6. 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.

  7. IUPAC nomenclature of organic chemistry - Wikipedia

    en.wikipedia.org/wiki/IUPAC_nomenclature_of...

    The secondary functional groups are: a hydroxy- at carbon 5, a chloro- at carbon 11, a methoxy- at carbon 15, and a bromo- at carbon 18. Grouped with the side chains, this gives 18-bromo-12-butyl-11-chloro-4,8-diethyl-5-hydroxy-15-methoxy. There are two double bonds: one between carbons 6 and 7, and one between carbons 13 and 14.

  8. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    For example, 1-bromo-1-fluoroethane can undergo nucleophilic attack to form 1-fluoroethan-1-ol, with the nucleophile being an HO − group. In this case, if the reactant is levorotatory, then the product would be dextrorotatory, and vice versa. [3] S N 2 mechanism of 1-bromo-1-fluoroethane with one of the carbon atoms being a chiral centre.

  9. Bromopentane - Wikipedia

    en.wikipedia.org/wiki/Bromopentane

    Monobromopentanes are bromopentanes containing one bromine atom, with the formula C 5 H 11 Br. There are three isomers of unbranched monobromopentane: 1-Bromopentane; 2-Bromopentane [1] (chiral) 3-Bromopentane; There are four isomers of monobromopentane based on 2-methylbutane: 1-Bromo-2-methylbutane (chiral) 1-Bromo-3-methylbutane; 2-Bromo-2 ...