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  2. Acetic acid - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid

    acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...

  3. TAE buffer - Wikipedia

    en.wikipedia.org/wiki/TAE_buffer

    TAE buffer is commonly prepared as a 50× stock solution for laboratory use. A 50× stock solution can be prepared by dissolving 242 g Tris base in water, adding 57.1 ml glacial acetic acid, and 100 ml of 500 mM EDTA (pH 8.0) solution, and bringing the final volume up to 1 litre.

  4. Acetic acid (data page) - Wikipedia

    en.wikipedia.org/wiki/Acetic_acid_(data_page)

    2 Structure and properties. 3 Thermodynamic properties. ... Vapor-liquid Equilibrium for Acetic acid/Water [3] P = 760 mm Hg BP Temp. °C mole % water liquid vapor ...

  5. Glacial acetic acid - Wikipedia

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

    This page was last edited on 14 September 2019, at 22:01 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  6. Acetyl-CoA - Wikipedia

    en.wikipedia.org/wiki/Acetyl-CoA

    Acetyl-CoA then enters the citric acid cycle, where the acetyl group is oxidized to carbon dioxide and water, and the energy released is captured in the form of 11 ATP and one GTP per acetyl group. Konrad Bloch and Feodor Lynen were awarded the 1964 Nobel Prize in Physiology or Medicine for their discoveries linking acetyl-CoA and fatty acid ...

  7. Manganese(II) acetate - Wikipedia

    en.wikipedia.org/wiki/Manganese(II)_acetate

    Manganese(II) acetate can be formed by treating either manganese(II,III) oxide or manganese(II) carbonate with acetic acid: [4] Mn 3 O 4 + 2 CH 3 CO 2 H → Mn(CH 3 CO 2) 2 + Mn 2 O 3 + H 2 O MnCO 3 + 2 CH 3 CO 2 H → Mn(CH 3 CO 2) 2 + CO 2 + H 2 O

  8. Zenker's fixative - Wikipedia

    en.wikipedia.org/wiki/Zenker's_fixative

    If the glacial acetic acid is replaced by 5 ml of formalin (37–40% formaldehyde), the resulting solution is Helly's fixative, also sometimes called "formol-Zenker".Helly is stable for only a few hours because the formaldehyde and dichromate components react, producing formic acid and chromium(III) ions; the orange solution becomes greenish.

  9. Cellulose acetate - Wikipedia

    en.wikipedia.org/wiki/Cellulose_acetate

    However, acetic acid is usually also formed as a by-product of the reaction, so that the solvent is ultimately a mixture of methylene chloride, acetic anhydride and acetic acid. A very rare heterogeneous process is the fiber acetate process, which is only used for the production of cellulose triacetate as an end product.