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  2. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    Instead, the rate equation may be more accurately described using steady-state kinetics. The reaction involves a carbocation intermediate and is commonly seen in reactions of secondary or tertiary alkyl halides under strongly basic conditions or, under strongly acidic conditions, with secondary or tertiary alcohols .

  3. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    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. This mechanism always results in inversion of configuration.

  4. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    Competition experiment between SN2 and E2. With ethyl bromide, the reaction product is predominantly the substitution product. As steric hindrance around the electrophilic center increases, as with isobutyl bromide, substitution is disfavored and elimination is the predominant reaction. Other factors favoring elimination are the strength of the ...

  5. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    The rate equation for this reaction would be Rate=k[Sub][Nuc]. For a S N 2 reaction, an aprotic solvent is best, such as acetone, DMF, or DMSO. Aprotic solvents do not add protons (H + ions) into solution; if protons were present in S N 2 reactions, they would react with the nucleophile and severely limit the reaction rate.

  6. Associative substitution - Wikipedia

    en.wikipedia.org/wiki/Associative_substitution

    The terminology is typically applied to organometallic and coordination complexes, but resembles the Sn2 mechanism in organic chemistry. The opposite pathway is dissociative substitution, being analogous to the Sn1 pathway. Intermediate pathways exist between the pure associative and pure dissociative pathways, these are called interchange ...

  7. Cheap and deadly: Why vehicle terror attacks like the Bourbon ...

    www.aol.com/cheap-deadly-why-vehicle-terror...

    Experts say vehicle-based attacks are simple for a 'lone wolf' terrorist to plan and execute, and challenging for authorities to prevent.

  8. SNi - Wikipedia

    en.wikipedia.org/wiki/SNi

    The difference between S N 1 and S N i is actually that the ... S N i reaction mechanism Sn1 occurs in tertiary carbon while Sn2 occurs in primary carbon. See also ...

  9. Choking emergency? How to do the Heimlich maneuver - AOL

    www.aol.com/choking-emergency-heimlich-maneuver...

    Next, thrust in an inward and upward motion on the diaphragm. This will force air out of the lungs and remove the blockage. Repeat these abdominal thrusts up to five times, the doctor advised.