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  2. List of acids by Hammett acidity - Wikipedia

    en.wikipedia.org/wiki/List_of_acids_by_hammett...

    This article was nominated for deletion. The discussion was closed on 26 December 2024 with a consensus to merge the content into the article Hammett acidity function.If you find that such action has not been taken promptly, please consider assisting in the merger instead of re-nominating the article for deletion.

  3. Organic acid - Wikipedia

    en.wikipedia.org/wiki/Organic_acid

    Simple organic acids like formic or acetic acids are used for oil and gas well stimulation treatments. These organic acids are much less reactive with metals than are strong mineral acids like hydrochloric acid (HCl) or mixtures of HCl and hydrofluoric acid (HF). For this reason, organic acids are used at high temperatures or when long contact ...

  4. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    Stronger acids have a larger and a smaller logarithmic constant (= ⁡) than weaker acids. The stronger an acid is, the more easily it loses a proton, H + {\displaystyle {\ce {H+}}} . Two key factors that contribute to the ease of deprotonation are the polarity of the H − A {\displaystyle {\ce {H-A}}} bond and the size of atom A, which ...

  5. Category:Acids - Wikipedia

    en.wikipedia.org/wiki/Category:Acids

    Pages in category "Acids" The following 35 pages are in this category, out of 35 total. This list may not reflect recent changes. ...

  6. Naphthenic acid - Wikipedia

    en.wikipedia.org/wiki/Naphthenic_acid

    Naphthenic acids are represented by a general formula C n H 2n-z O 2, where n indicates the carbon number and z specifies a homologous series. The z is equal to 0 for saturated, acyclic acids and increases to 2 in monocyclic naphthenic acids, to 4 in bicyclic naphthenic acids, to 6 in tricyclic acids, and to 8 in tetracyclic acids. [5]

  7. Nucleotide - Wikipedia

    en.wikipedia.org/wiki/Nucleotide

    This nucleotide contains the five-carbon sugar deoxyribose (at center), a nucleobase called adenine (upper right), and one phosphate group (left). The deoxyribose sugar joined only to the nitrogenous base forms a Deoxyribonucleoside called deoxyadenosine, whereas the whole structure along with the phosphate group is a nucleotide, a constituent of DNA with the name deoxyadenosine monophosphate.

  8. Nucleic acid - Wikipedia

    en.wikipedia.org/wiki/Nucleic_acid

    Nucleic acids are chemical compounds that are found in nature. They carry information in cells and make up genetic material. These acids are very common in all living things, where they create, encode, and store information in every living cell of every life-form on Earth. In turn, they send and express that information inside and outside the ...

  9. Purine - Wikipedia

    en.wikipedia.org/wiki/Purine

    The starting material for the reaction sequence was uric acid (8), which had been isolated from kidney stones by Carl Wilhelm Scheele in 1776. [12] Uric acid was reacted with PCl 5 to give 2,6,8-trichloropurine, which was converted with HI and PH 4 I to give 2,6-diiodopurine.