enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    The classic example of a dehydration reaction is the Fischer esterification, which involves treating a carboxylic acid with an alcohol to give an ester RCO 2 H + R′OH ⇌ RCO 2 R′ + H 2 O Often such reactions require the presence of a dehydrating agent, i.e. a substance that reacts with water.

  3. Tin(II) chloride - Wikipedia

    en.wikipedia.org/wiki/Tin(II)_chloride

    Tin(II) chloride dissolves in less than its own mass of water. Dilute solutions are subject to hydrolysis, yielding an insoluble basic salt: SnCl 2 + H 2 O ⇌ Sn(OH)Cl + HCl. Hydrolysis is prevented in the presence of hydrochloric acid, typically of the same or greater molarity as the

  4. Condensation reaction - Wikipedia

    en.wikipedia.org/wiki/Condensation_reaction

    Condensation reactions likely played major roles in the synthesis of the first biotic molecules including early peptides and nucleic acids. In fact, condensation reactions would be required at multiple steps in RNA oligomerization: the condensation of nucleobases and sugars, nucleoside phosphorylation, and nucleotide polymerization. [6]

  5. Benzaldehyde oxime - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde_oxime

    Its dehydration yields benzonitrile. It can be hydrolyzed to regenerate benzaldehyde. [5] It reacts with N-chlorosuccinimide in DMF to form benzohydroximoyl chloride, in which chlorine replaces hydrogen on the carbon attached to the nitrogen in benzaldehyde oxime. [6]

  6. Peptide bond - Wikipedia

    en.wikipedia.org/wiki/Peptide_bond

    Peptide bond formation via dehydration reaction. When two amino acids form a dipeptide through a peptide bond, [1] it is a type of condensation reaction. [2] In this kind of condensation, two amino acids approach each other, with the non-side chain (C1) carboxylic acid moiety of one coming near the non-side chain (N2) amino moiety of the other.

  7. Aldol condensation - Wikipedia

    en.wikipedia.org/wiki/Aldol_condensation

    Dehydration may be accompanied by decarboxylation when an activated carboxyl group is present. The aldol addition product can be dehydrated via two mechanisms; a strong base like potassium t -butoxide , potassium hydroxide or sodium hydride deprotonates the product to an enolate , which eliminates via the E1cB mechanism , [ 9 ] [ 10 ] while ...

  8. Chemiosmosis - Wikipedia

    en.wikipedia.org/wiki/Chemiosmosis

    A Proton Gradient Powers the Synthesis of ATP". Biochemistry (5th ed.). W. H. Freeman. A set of experiments aiming to test some tenets of the chemiosmotic theory – Ogawa S, Lee TM (August 1984). "The relation between the internal phosphorylation potential and the proton motive force in mitochondria during ATP synthesis and hydrolysis".

  9. Dehydration synthesis - Wikipedia

    en.wikipedia.org/?title=Dehydration_synthesis&...

    Retrieved from "https://en.wikipedia.org/w/index.php?title=Dehydration_synthesis&oldid=272235332"This page was last edited on 21 February 2009, at 09:33