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  2. Pyrrole - Wikipedia

    en.wikipedia.org/wiki/Pyrrole

    Pyrrole is an extremely weak base for an amine, with a conjugate acid pK a of −3.8. The most thermodynamically stable pyrrolium cation (C 4 H 6 N +) is formed by protonation at the 2 position. Substitution of pyrrole with alkyl substituents provides a more basic molecule—for example, tetramethylpyrrole has a conjugate acid pK a of +3.7.

  3. Pyrotechnic composition - Wikipedia

    en.wikipedia.org/wiki/Pyrotechnic_composition

    High-temperature flame with solid particles, which interfere with flame colorants. Reacts with nitrates, except ammonium nitrate, yielding nitrogen oxides, ammonia, and heat (the reaction is slow at room temperature but violent at above 80 °C and may spontaneously ignite); the reaction can be inhibited by a weak acid, e.g. boric acid. Corroded ...

  4. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    For example, acetic acid is a weak acid which has a = 1.75 x 10 −5. Its conjugate base is the acetate ion with K b = 10 −14 /K a = 5.7 x 10 −10 (from the relationship K a × K b = 10 −14), which certainly does not correspond to a strong base. The conjugate of a weak acid is often a weak base and vice versa.

  5. Knorr pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Knorr_pyrrole_synthesis

    Dissolving Knorr's pyrrole in concentrated sulfuric acid, and then pouring the resulting solution into water will hydrolyze the 4-ester group selectively. The 5-methyl group can be variously oxidized to chloromethyl, aldehyde, or carboxylic acid functionality by the use of stoichiometric sulfuryl chloride in glacial acetic acid. [7]

  6. Polypyrrole - Wikipedia

    en.wikipedia.org/wiki/Polypyrrole

    Polypyrrole Pyrrole can be polymerised electrochemically. [1] Polypyrrole (PPy) is an organic polymer obtained by oxidative polymerization of pyrrole. It is a solid with the formula H(C 4 H 2 NH) n H. It is an intrinsically conducting polymer, used in electronics, optical, biological and medical fields. [2] [3]

  7. Rothemund reaction - Wikipedia

    en.wikipedia.org/wiki/Rothemund_reaction

    The reaction employs an organic acidic medium such as acetic acid or propionic acid as typical reaction solvents. Alternatively p-toluenesulfonic acid or various Lewis acids can be used with chlorinated solvents. The aldehyde and pyrrole are heated in this medium to afford modest yields of the meso tetrasubstituted porphyrins [RCC 4 H 2 N] 4 H 2.

  8. AOL Mail - AOL Help

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    Get answers to your AOL Mail, login, Desktop Gold, AOL app, password and subscription questions. Find the support options to contact customer care by email, chat, or phone number.

  9. Tetrapyrrole - Wikipedia

    en.wikipedia.org/wiki/Tetrapyrrole

    Tetrapyrroles are a class of chemical compounds that contain four pyrrole or pyrrole-like rings. The pyrrole/pyrrole derivatives are linked by (= (CH)-or -CH 2-units), in either a linear or a cyclic fashion. Pyrroles are a five-atom ring with four carbon atoms and one nitrogen atom.