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- ...reduce benzophenone to produce the benzophenone ketyl radical, which is a strong blue color. The ketyl is very reactive and is destroyed by traces of water | style="text-align:center;"| Acids, base-sensitive solvents, nitromethane19 KB (2,493 words) - 16:52, 25 July 2023
- ...sium metal will slowly react with water, and far more quickly with mineral acids, at room temperature to release [[hydrogen]]: However, dysprosium dissolves only slowly in weak acids, like [[acetic acid]] or [[citric acid]], even when concentrated.9 KB (1,207 words) - 17:52, 23 June 2019
- ...oducing an ester from an [[alcohol]] and a [[carboxylic acid]]. Carboxylic acids and alcohols esterify in small amounts according to a reversible equation: ...owards the right. Sulfuric acid is useful in this way too, as it acts as a strong dehydrating agent, sequestering water. The reaction rate is greatly increas2 KB (340 words) - 15:26, 6 April 2022
- Chlorine is a strong oxidizer with 7 valence [[electron]]s. Its unstable [[electron configuratio ...terials. It is notorious for reacting with iron at high temperatures, in a strong exothermic reaction, known as chlorine-iron fire.13 KB (1,873 words) - 17:48, 8 November 2023
- ...en forming pleasant-smelling compounds such as [[methyl formate]]. Being a strong acid, esterifications with formic acid generally don't require an acid cata .../viewthread.php?tid=35568 Handling Formic Acid? Strength compared to other acids?]8 KB (996 words) - 15:05, 18 November 2023
- ...the lanthanides, is quite electropositive. It dissolves in acids, weak and strong, without hesitation.8 KB (1,067 words) - 18:03, 31 January 2023
- Gallium is attacked by acids and free halogens, but does not react with air or water at room temperature Gallium(I) oxide is a strong reducing agent, capable of reducing [[sulfuric acid]] to [[hydrogen sulfide9 KB (1,282 words) - 23:20, 17 January 2018
- ...ced by the hydrolysis, or saponification, of plant and animal fats using a strong base, such as [[sodium hydroxide]]. It is usually simpler to purchase it ra6 KB (707 words) - 14:50, 18 November 2023
- ...[lead(II) sulfate]] on addition of the corresponding strong [[Acid|mineral acids]], but [[lead(II) nitrate]] will not precipitate in this way, due to relati8 KB (1,127 words) - 00:10, 11 December 2019
- ...ic]]. It will react with acids to form lead(II) salts and will dissolve in strong bases to form the plumbite (PbO<sub>2</sub><sup>2-</sup>) anion, which can5 KB (592 words) - 17:58, 8 November 2023
- ...reducing agents or organic compounds. It may also be decomposed by strong acids.5 KB (623 words) - 18:58, 9 November 2018
- ...rganic compound with the chemical formula '''LiAlH<sub>4</sub>'''. It is a strong reducing agent used in organic chemistry. ...ines. LAH is most commonly used for the reduction of esters and carboxylic acids to primary alcohols.6 KB (799 words) - 17:39, 29 February 2020
- Manganese dioxide is a moderately strong oxidizing agent, and is used as such in the lab. It may be hydrated, but de ...acids such as [[nitric acid|nitric]] or [[sulfuric acid]], though halogen acids will attack it. The reaction also releases the halogen from its respective7 KB (902 words) - 14:54, 18 November 2023
- ...h as aromatic compounds. The sulfuric acid in this mixture is sufficiently strong to protonate nitric acid, producing the [[nitronium]] ion (NO<sub>2</sub><s [[Category:Acids]]2 KB (258 words) - 20:07, 10 October 2015
- Neodymium oxalate is inert to most strong acids, including but not limited to concentrated [[Hydrochloric acid|hydrochloric5 KB (538 words) - 15:21, 10 July 2019
- As a nitrogenous base, nicotine forms salts with acids, that are usually solid and water-soluble. Nicotine is biodegradable. Its decomposition is accelerated with strong UV light.7 KB (849 words) - 15:23, 22 August 2020
- '''Nitric acid''' is a strong acid with the formula '''HNO<sub>3</sub>'''. It is an important [[mineral a ...being tested, and then heating the mixture. If proteins that contain amino acids with aromatic rings are present, the mixture turns yellow. Upon adding a ba12 KB (1,686 words) - 11:53, 23 September 2023
- ...ic reaction, or by reacting a nitrate salt with hot or concentrated strong acids. It is also produced as a side-product of nitrations or when nitric acid is6 KB (825 words) - 18:56, 12 October 2018
- ...ensitive to impact, but incomplete detonation result from everything but a strong initiation. This causes its lead block test value to be dependent on the st ...even more sensitive. It is also toxic by skin contact and inhalation. As a strong vasodilator, it results in severe headaches, though it is used medicinally7 KB (807 words) - 12:55, 27 February 2024
- Nitromethane will not react with strong oxidizers like [[manganese heptoxide]]. This was observed by many SM member When refluxed with mineral acids, nitromethane, much like higher primary nitroparaffins, decomposes to form10 KB (1,375 words) - 20:01, 16 May 2023