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  2. Pinner reaction - Wikipedia

    en.wikipedia.org/wiki/Pinner_reaction

    For example: an electron-poor nitrile is a good electrophile (readily susceptible to attack from alkoxides etc.) but a poor nucleophile would typically be easier to protonate than to participate in the reaction and hence would be expected to react more readily under basic rather than acidic conditions.

  3. Electrophile - Wikipedia

    en.wikipedia.org/wiki/Electrophile

    In chemistry, an electrophile is a chemical species that forms bonds with nucleophiles by accepting an electron pair. [1] Because electrophiles accept electrons, they are Lewis acids . [ 2 ] Most electrophiles are positively charged , have an atom that carries a partial positive charge, or have an atom that does not have an octet of electrons.

  4. Sulfonium-based oxidation of alcohols to aldehydes - Wikipedia

    en.wikipedia.org/wiki/Sulfonium-based_oxidation...

    The sulfonium oxidations can be categorized into two groups: The methods discovered earliest rely on activated alcohols like alkyl tosylates (Kornblum oxidation) [2] or alkyl chloroformates (from reaction of alcohols with phosgene: Barton-Kornblum) [3] that react as electrophiles when treated with DMSO, liberating an oxygenated leaving group (e.g. OTs−).

  5. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    In chemistry, an alcohol (from Arabic al-kuḥl 'the kohl'), [2] is a type of organic compound that carries at least one hydroxyl (−OH) functional group bound to a saturated carbon atom. [3] [4] Alcohols range from the simple, like methanol and ethanol, to complex, like sugars and cholesterol. The presence of an OH group strongly modifies the ...

  6. Carboximidate - Wikipedia

    en.wikipedia.org/wiki/Carboximidate

    Carboximidates are good electrophiles and undergo a range of addition reactions; with aliphatic imidates generally reacting faster than aromatic imidates. [2] They can be hydrolyzed to give esters and by an analogous process react with amines (including ammonia) to form amidines.

  7. What is sugar alcohol and is it bad for you? Here's the ...

    www.aol.com/sugar-alcohol-reduced-calorie...

    Sugar alcohols are safe to consume, but only in moderation. The Cleveland Clinic says 10 to 15 grams a day is a safe amount. ... Gift cards that make good last-minute gifts, done and dusted. AOL.

  8. Electrophilic aromatic substitution - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_aromatic...

    Other electrophiles are aromatic diazonium salts in diazonium couplings, carbon dioxide in the Kolbe–Schmitt reaction and activated carbonyl groups in the Pechmann condensation, hydroxycarbenium ion in the Blanc chloromethylation via an intermediate (hydroxymethyl)arene (benzyl alcohol), chloryl cation (ClO 3 +) for electrophilic perchlorylation.

  9. What Happens to Your Body When You Drink Alcohol Regularly

    www.aol.com/lifestyle/happens-body-drink-alcohol...

    Is alcohol good or bad for health? Moderate red wine consumption may support some aspects of heart health. However, excessive alcohol consumption is linked to headaches, nausea, poor coordination ...