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  2. SN2 reaction - Wikipedia

    en.wikipedia.org/wiki/SN2_reaction

    The methoxide anion, for example, is both a strong base and nucleophile because it is a methyl nucleophile, and is thus very much unhindered. tert -Butoxide , on the other hand, is a strong base, but a poor nucleophile, because of its three methyl groups hindering its approach to the carbon.

  3. Nucleophilic substitution - Wikipedia

    en.wikipedia.org/wiki/Nucleophilic_substitution

    The nucleophile may be electrically neutral or negatively charged, whereas the substrate is typically neutral or positively charged. An example of nucleophilic substitution is the hydrolysis of an alkyl bromide , R-Br under basic conditions, where the attacking nucleophile is hydroxyl ( OH − ) and the leaving group is bromide ( Br − ).

  4. Nucleophile - Wikipedia

    en.wikipedia.org/wiki/Nucleophile

    A hydroxide ion acting as a nucleophile in an S N 2 reaction, converting a haloalkane into an alcohol. In chemistry, a nucleophile is a chemical species that forms bonds by donating an electron pair. All molecules and ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they ...

  5. A normal cholesterol level can still be deadly, warns healthy ...

    www.aol.com/finance/normal-cholesterol-level...

    Normal LDL cholesterol levels are associated with the build-up of atherosclerotic plaques in our arteries even in those with so-called optimal risk factors by current standards: blood pressure ...

  6. Why High Cholesterol Isn't Always Bad, According to Cardiologists

    www.aol.com/why-high-cholesterol-isnt-always...

    LDL cholesterol is the “badcholesterol that can increase the risk of heart disease and stroke when levels are too high. HDL cholesterol is “good” cholesterol and high levels of it can ...

  7. Alpha effect - Wikipedia

    en.wikipedia.org/wiki/Alpha_effect

    This is because α-nucleophiles showing the α-effect have smaller HOMO(nucleophile)-LUMO(substrate) gap, in other words, high HOMO energy level that allows more orbital interaction. Examples of α-nucleophiles with α-effects are shown in Figure 4. The α-nucleophiles have smaller HOMO lobes than the parent normal nucleophile. Figure 4.

  8. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    The rate equation for S N 2 reactions are bimolecular being first order in Nucleophile and first order in Reagent. The determining factor when both S N 2 and S N 1 reaction mechanisms are viable is the strength of the Nucleophile. Nuclephilicity and basicity are linked and the more nucleophilic a molecule becomes the greater said nucleophile's ...

  9. LDL cholesterol is known as “badcholesterol, while HDL cholesterol is generally considered “good” cholesterol. But a new study has found that HDL cholesterol isn’t as protective ...