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  2. Conjugate (acid-base theory) - Wikipedia

    en.wikipedia.org/wiki/Conjugate_(acid-base_theory)

    One use of conjugate acids and bases lies in buffering systems, which include a buffer solution. In a buffer, a weak acid and its conjugate base (in the form of a salt), or a weak base and its conjugate acid, are used in order to limit the pH change during a titration process. Buffers have both organic and non-organic chemical applications.

  3. Conjugated system - Wikipedia

    en.wikipedia.org/wiki/Conjugated_system

    Cinnamaldehyde is a naturally-occurring compound that has a conjugated system penta-1,3-diene is a molecule with a conjugated system Diazomethane conjugated pi-system. In theoretical chemistry, a conjugated system is a system of connected p-orbitals with delocalized electrons in a molecule, which in general lowers the overall energy of the molecule and increases stability.

  4. Perchlorate - Wikipedia

    en.wikipedia.org/wiki/Perchlorate

    Perchlorate salts are typically manufactured through the process of electrolysis, which involves oxidizing aqueous solutions of corresponding chlorates.This technique is commonly employed in the production of sodium perchlorate, which finds widespread use as a key ingredient in rocket fuel. [5]

  5. Michael addition reaction - Wikipedia

    en.wikipedia.org/wiki/Michael_Addition_Reaction

    In organic chemistry, the Michael reaction or Michael 1,4 addition is a reaction between a Michael donor (an enolate or other nucleophile) and a Michael acceptor (usually an α,β-unsaturated carbonyl) to produce a Michael adduct by creating a carbon-carbon bond at the acceptor's β-carbon.

  6. Bioconjugation - Wikipedia

    en.wikipedia.org/wiki/Bioconjugation

    The nucleophilic lysine residue is commonly targeted site in protein bioconjugation, typically through amine-reactive N-hydroxysuccinimidyl (NHS) esters. [3] To obtain optimal number of deprotonated lysine residues, the pH of the aqueous solution must be below the pKa of the lysine ammonium group, which is around 10.5, so the typical pH of the reaction is about 8 and 9.

  7. Oxalic acid - Wikipedia

    en.wikipedia.org/wiki/Oxalic_acid

    The conjugate base of oxalic acid is the hydrogenoxalate anion, and its conjugate base is a competitive inhibitor of the lactate dehydrogenase (LDH) enzyme. [48] LDH catalyses the conversion of pyruvate to lactic acid (end product of the fermentation (anaerobic) process) oxidising the coenzyme NADH to NAD + and H + concurrently.

  8. Study links mental health risks to this toxin for those born ...

    www.aol.com/study-links-mental-health-risks...

    Lead exposure in the 20th century may have led to mental health issues in Americans, a new study suggests.. Researchers from Duke University and Florida State University studied the impact of lead ...

  9. Carboxylic acid - Wikipedia

    en.wikipedia.org/wiki/Carboxylic_acid

    Heating the salt to above 100 °C will drive off water and lead to the formation of the amide. This method of synthesizing amides is industrially important, and has laboratory applications as well. [9] In the presence of a strong acid catalyst, carboxylic acids can condense to form acid anhydrides. The condensation produces water, however ...