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  2. SN1 reaction - Wikipedia

    en.wikipedia.org/wiki/SN1_reaction

    Typical polar protic solvents include water and alcohols, which will also act as nucleophiles, and the process is known as solvolysis. The Y scale correlates solvolysis reaction rates of any solvent ( k ) with that of a standard solvent (80% v/v ethanol / water ) ( k 0 ) through

  3. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    The solvent affects the rate of reaction because solvents may or may not surround a nucleophile, thus hindering or not hindering its approach to the carbon atom. [6] Polar aprotic solvents, like tetrahydrofuran , are better solvents for this reaction than polar protic solvents because polar protic solvents will hydrogen bond to the nucleophile ...

  4. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    In chemistry, solvent effects are the influence of a solvent on chemical reactivity or molecular associations. Solvents can have an effect on solubility , stability and reaction rates and choosing the appropriate solvent allows for thermodynamic and kinetic control over a chemical reaction.

  5. Solvolysis - Wikipedia

    en.wikipedia.org/wiki/Solvolysis

    Ammonia boils at −33 °C, and, as such, is rarely used as a solvent in its pure form. It is, however, readily miscible with water, and is commonly used in the form of a saturated aqueous solution. For this reason, ammonolysis may be considered as a special case of solvolysis, as the ammonia is itself dissolved in a solvent.

  6. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    In chemistry, a nucleophilic substitution (S N) is a class of chemical reactions in which an electron-rich chemical species (known as a nucleophile) replaces a functional group within another electron-deficient molecule (known as the electrophile). The molecule that contains the electrophile and the leaving functional group is called the substrate.

  7. Nucleophilic aromatic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_aromatic...

    A nucleophilic aromatic substitution (S N Ar) is a substitution reaction in organic chemistry in which the nucleophile displaces a good leaving group, such as a halide, on an aromatic ring. Aromatic rings are usually nucleophilic, but some aromatic compounds do undergo nucleophilic substitution.

  8. This is why you should give your dog choices when training ...

    www.aol.com/why-dog-choices-training-them...

    When you’re training a dog, it’s vital to gain their trust. If a dog feels like they’re being forced to do something, they might find the situation more stressful or appear stubborn – so ...

  9. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    Substitution reactions in organic chemistry are classified either as electrophilic or nucleophilic depending upon the reagent involved, whether a reactive intermediate involved in the reaction is a carbocation, a carbanion or a free radical, and whether the substrate is aliphatic or aromatic. Detailed understanding of a reaction type helps to ...