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  • ...concentrating the potassium hydroxide. Another inconvenient represents the organic residues from the wood ash, which are difficult to remove. They can however [[Category:Bases]]
    8 KB (1,005 words) - 16:52, 17 August 2023
  • ...xides that behave like alkali metal hydroxides; these are typically strong bases.
    2 KB (367 words) - 18:22, 2 January 2023
  • ...gent that causes immediate and highly exothermic charring of virtually any organic material it comes into contact with. Sulfur trioxide reacts with water in t ...ard protection clothing is insufficient, as the acid mist will attack most organic fibers as well as wreck most air filtration systems and may condense on the
    11 KB (1,598 words) - 23:45, 25 August 2020
  • ...in dark, well ventilated areas. Keep it away from any flammable materials, bases, acids. Since it gives off chlorine over time, keep it in a separate place [[Category:Organic compounds]]
    6 KB (728 words) - 09:53, 13 July 2022
  • ...oduced from inorganic chemicals, a breakthrough in chemistry, which proved organic substances can be produced from inorganic substances, disproving the notion Urea is a weak organic base. It forms salts with strong acids.<ref>
    8 KB (1,070 words) - 13:27, 10 July 2022
  • '''Hexamine''' (or '''methenamine''') is a solid, flammable organic compound that finds a use as a starting point for a few energetic materials Reactions with [[hydrogen peroxide]] form a very unstable organic peroxide explosive, similar to [[acetone peroxide]], called [[Hexamethylene
    8 KB (1,003 words) - 14:48, 18 November 2023
  • ...o hydrolyze, producing hydrogen chloride gas. It is a popular catalyst for organic synthesis, and the most common printed circuit board etchant (though there ...acid, iron(III) chloride is corrosive and readily forms adducts with Lewis bases, such as triphenylphosphine oxide. It will also dissolve in methanol and et
    8 KB (1,071 words) - 14:38, 18 November 2023
  • '''Pyridine''', also known as '''azine''', is an organic compound consisting of a [[benzene]] ring with one =CH- group being replace ...ives, [[2,2'-bipyridine]] and [[terpyridine]]. Stronger [[lewis base|Lewis bases]] can be subsituted for these ligands, making these complexes useful precur
    7 KB (974 words) - 17:44, 30 November 2022
  • ...an unusual problem in that it is lighter than almost every single nonpolar organic solvent. The only ones in which it sinks are liquid [[ethane]] and [[methan ...m is more reactive than lithium, but it's denser than mineral oil and most organic solvents and can be easily stored for months.
    48 KB (5,818 words) - 20:11, 13 March 2024
  • ...rbonate is a white hydgoscopic compound, soluble in water but insoluble in organic solvents. It reacts with acids, sulfur and nitrogen oxides, as well as halo As a basic sodium compound, the addition of most inorganic and some organic acids yields a sodium salt of that acid, and due to the almost universal so
    10 KB (1,368 words) - 14:39, 18 November 2023
  • ...briefly produces a deep blue or violet coloration upon addition to strong bases such as [[ammonia]]. ...ncentrations. It is only very slightly soluble in lower alcohols and other organic solvents, but solubility increases slightly with the addition of acids.
    5 KB (539 words) - 22:20, 11 November 2020
  • Sodium bicarbonate reacts with bases such as sodium hydroxide to form carbonates: ...m bicarbonate to be useful as a safe neutralizing agent for both acids and bases.
    7 KB (901 words) - 08:41, 30 May 2020
  • ...'' (IUPAC name: '''2-hydroxypropane-1,2,3-tricarboxylic acid''') is a weak organic acid, mostly used in the food industry, where it serves as a preservative a Citric acid will react in solution with bases, carbonates and bicarbonates, as well as reactive metals, such as [[magnesi
    7 KB (884 words) - 18:00, 29 December 2023
  • ...aponification, which is used in soapmaking, sodium hydroxide can hydrolyze organic esters such as those found in naturally occurring plant or animal fats, pro Sodium hydroxide and sometimes other strong bases are used to [[gas scrubber|scrub gases]] such as [[hydrogen chloride]]/[[hy
    13 KB (1,867 words) - 14:45, 18 November 2023
  • ...Other = Reacts with acids, bases, halogens, SO<sub>2</sub><br>Insoluble in organic solvents [[Category:Bases]]
    6 KB (729 words) - 10:49, 27 October 2019
  • '''Dimethylamine''' is an organic compound with the formula '''(CH<sub>3</sub>)<sub>2</sub>NH''', an amine. ...[[dimethylformamide]].<ref>Weissermel, K.; Arpe, H.-J. (2003). Industrial Organic Chemistry: Important Raw Materials and Intermediates. Wiley-VCH. pp. 45–4
    8 KB (1,050 words) - 13:47, 26 August 2023
  • ...light organic materials on fire. It is also a strong acid. It reacts with bases to form chlorate salts. ...e same concentrations. It is also known to react violently with oxidizable organic materials. The products of its decomposition are toxic gases. Its ability t
    7 KB (861 words) - 21:15, 11 August 2023
  • ...form a new bond with a [[Lewis acid]]. All Brønsted-Lowry bases are Lewis bases, as they can accept protons as well as other electron deficient species. Lewis bases are split in three categories:
    1 KB (179 words) - 20:02, 10 April 2023
  • ...that behaves similarly to litmus. It is actually a whole family of related organic compounds; the most useful particular anthocyanins are '''cyanidin''' (foun ...ns, yellowish-green in strongly basic ones). In addition, extremely strong bases cause anthocyanins to slowly degrade, turn yellow and lose their indicator
    5 KB (813 words) - 20:03, 21 July 2023
  • ...thylene triperoxide diamine''' or '''HMTD''' is a dangerous high explosive organic compound. It has very little use outside of amateur explosives, and because ...st common metals. HMTD is chemically very stable when pure (free of acids, bases, and metal ions) and does not quickly sublime like its acetone counterparts
    9 KB (1,169 words) - 10:36, 29 November 2020

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