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  • 6 KB (658 words) - 10:28, 27 December 2023
  • Acetic acid will react with alcohols in the presence of a catalyst, such as [[sulfuric acid]] to form [[ester]]s
    11 KB (1,554 words) - 14:43, 18 November 2023
  • | SolubleOther = Soluble in alcohols
    6 KB (827 words) - 15:31, 20 May 2020
  • 6 KB (692 words) - 13:57, 18 November 2023
  • '''Alcohols''' are organic compounds which contain a hydroxyl functional group (-OH) bo == Types of Alcohols ==
    6 KB (832 words) - 21:26, 29 June 2019
  • Many alkyl alcohols will dehydrate to an [[ester]] on addition of [[nitric acid]] with loss of
    2 KB (205 words) - 17:55, 24 January 2020
  • ...xylic acids and is the reagent of choice from the bromination of sensitive alcohols. Both of these reactions occur via a [[phosphorus tribromide]]; alternative
    14 KB (1,973 words) - 11:41, 25 June 2023
  • *Butyl alcohols
    5 KB (569 words) - 19:01, 25 September 2022
  • [[Category:Alcohols]] [[Category:Primary alcohols]]
    7 KB (908 words) - 21:07, 12 September 2019
  • ...lacial acetic acid]], a useful reagent. Calcium acetate will also gel many alcohols if mixed in correct proportions. Too much calcium acetate will revert the g
    5 KB (677 words) - 15:15, 18 November 2023
  • | SolubleOther = Reacts with alcohols, carboxylic acids, mineral acids<br>Insoluble in all solvents ...es, is a superbase. It is capable of deprotonating not just water but also alcohols, evolving acetylene.
    9 KB (1,277 words) - 13:58, 18 November 2023
  • * Make [[calcium acetate]] for gelling alcohols and production of [[acetone]]
    10 KB (1,377 words) - 19:55, 9 September 2023
  • * Remove alcohols from esters (from the reaction product of esterifications)
    8 KB (1,076 words) - 21:01, 22 March 2021
  • ...er = Reacts with acids<br>Slightly soluble in [[glycerol]]<br>Insoluble in alcohols, alkanes
    8 KB (1,050 words) - 20:51, 6 June 2018
  • ...lames after a few seconds. This reaction also works with many other simple alcohols and polyols like [[glycerol]] and some sugars. This is similar to the react
    6 KB (706 words) - 18:37, 2 June 2021
  • ...p://www.sciencemadness.org/talk/viewthread.php?tid=12655 Calcium oxide and alcohols/ethers]
    8 KB (1,039 words) - 23:42, 20 March 2020
  • 5 KB (608 words) - 11:11, 2 November 2019
  • ...d, soluble in water, with a sour taste. It is soluble in water, less so in alcohols, [[glycerol]], [[propylene glycol]], and insoluble in [[benzene]], [[chloro
    6 KB (692 words) - 19:51, 16 October 2022
  • 28 KB (2,574 words) - 17:03, 26 March 2019
  • 5 KB (543 words) - 22:36, 28 August 2018
  • Chromium(III) sulfate is readily soluble in water and some lower alcohols. ...hromate]] or [[sodium dichromate]] acidified with sulfuric acid to oxidize alcohols, produces chromium(III) sulfate as a byproduct, along with sodium or potass
    6 KB (795 words) - 16:52, 6 November 2018
  • ...dorless white crystalline solid, soluble in water, but almost insoluble in alcohols.
    5 KB (605 words) - 22:41, 17 October 2020
  • 7 KB (964 words) - 18:49, 28 March 2021
  • ...ith a pungent irritating odor, that fumes in air. It reacts with water and alcohols.
    5 KB (588 words) - 20:42, 22 November 2020
  • ...tion. Substances commonly used for this purpose include [[magnesium]] (for alcohols), [[calcium oxide]], [[calcium hydride]], [[phosphorus pentoxide]], and [[s ...20 to 50ppm). This technique is not compatible with protic solvents (like alcohols) or halogenated solvents, as these will react directly with the sodium. It
    19 KB (2,493 words) - 16:52, 25 July 2023
  • ...ester from an [[alcohol]] and a [[carboxylic acid]]. Carboxylic acids and alcohols esterify in small amounts according to a reversible equation:
    2 KB (340 words) - 15:26, 6 April 2022
  • ...carbonate]]. [[Calcium oxide]] can also be used. Ethanol, like most other alcohols, is highly flammable, even in low concentrations in solution, although at l [[Category:Alcohols]]
    14 KB (1,953 words) - 20:56, 9 September 2023
  • 6 KB (820 words) - 18:00, 5 August 2019
  • [[Category:Alcohols]]
    5 KB (501 words) - 13:36, 20 November 2020
  • ...ic acids, formic acid is easily [[esterification|esterified]] with primary alcohols, often forming pleasant-smelling compounds such as [[methyl formate]]. Bein
    8 KB (996 words) - 15:05, 18 November 2023
  • 6 KB (664 words) - 19:16, 25 November 2021
  • [[Category:Alcohols]] [[Category:Sugar alcohols]]
    6 KB (707 words) - 14:50, 18 November 2023
  • 8 KB (1,127 words) - 00:10, 11 December 2019
  • 5 KB (592 words) - 17:58, 8 November 2023
  • ...commonly used for the reduction of esters and carboxylic acids to primary alcohols. *Reducing esters to alcohols
    6 KB (799 words) - 17:39, 29 February 2020
  • ...s is rarer, as methanol is cheaper than the other alcohols. Some technical alcohols are nothing but almost pure MeOH mixed with dye. Methanol is significantly more toxic than other common alcohols such as [[ethanol]] or [[isopropanol]], as it is metabolized to [[formic ac
    11 KB (1,601 words) - 18:39, 9 July 2023
  • ...c Chemistry including Medicinal Chemistry, Mild and selective oxidation of alcohols and deoximation of oximes over supported quinolinium fluorochromate, Vol.43
    11 KB (1,468 words) - 18:42, 27 May 2023
  • ...s reactions, naphthalene can also be alkylated by reaction with alkenes or alcohols, with sulfuric or phosphoric acid as the catalyst.
    7 KB (924 words) - 15:02, 18 November 2023
  • | SolubleOther = Reacts with alcohols<br>Soluble in [[carbon tetrachloride]], [[chloroform]], [[nitric acid]]
    6 KB (825 words) - 18:56, 12 October 2018
  • ...poorly soluble in water, but miscible with other organic solvents, such as alcohols. It freezes at −29 °C and boils at around 100 °C.
    10 KB (1,375 words) - 20:01, 16 May 2023
  • 6 KB (801 words) - 17:05, 8 January 2020
  • | SolubleOther = Soluble in alcohols
    9 KB (1,223 words) - 00:12, 29 March 2020
  • 5 KB (667 words) - 12:48, 17 June 2019
  • ...o carbon dioxide and water. However, chromic acid will (violently) oxidize alcohols to their respective aldehydes or ketones, which cannot be oxidized further | style="text-align:center;"| Lots of water in an open space; low chain alcohols
    347 KB (46,057 words) - 20:09, 13 March 2024
  • ...m will slowly form. Other tertiary alcohols, and even bulk chain secondary alcohols have been shown to work just as good. The reaction mixture can then be dump
    13 KB (1,879 words) - 20:16, 17 September 2022
  • ...es oxidation]] to oxidize primary alcohols to [[aldehyde]]s, and secondary alcohols to [[ketone]]s. The dichromate is reduced to Cr(III) in these reactions, th
    10 KB (1,262 words) - 21:32, 16 October 2022
  • ...rong acids will oxidize primary alcohols to carboxylic acids and secondary alcohols to ketones. *Oxidize alcohols to carboxylic acids and ketones
    9 KB (1,171 words) - 21:27, 21 September 2023
  • [[Category:Alcohols]] [[Category:Primary alcohols]]
    4 KB (433 words) - 11:13, 9 June 2023
  • 9 KB (1,194 words) - 18:31, 3 February 2024
  • 6 KB (704 words) - 20:06, 21 January 2020
  • ...s in contact with open air. This compounds reacts violently with water and alcohols, releasing a fine mist of sulfuric acid and alkyl sulfates. It has a relati
    11 KB (1,598 words) - 23:45, 25 August 2020
  • ...ice of solvent. Recommended solvents are acetone and isopropanol, as lower alcohols will partially esterify with carboxylic acids, resulting in impurities and
    7 KB (1,088 words) - 20:32, 28 July 2015
  • 27 KB (4,285 words) - 21:31, 9 September 2023
  • ...ll form an azeotrope. Toluene is miscible with many organic solvents, like alcohols and esters. Toluene has a high refractive index, which causes it to exhibit
    7 KB (892 words) - 19:16, 15 September 2022
  • 8 KB (1,049 words) - 23:33, 14 July 2019
  • | SolubleOther = Reacts with acids and alkalis<br>Insoluble in alcohols, [[ester]]s, [[ether]]s, halocarbons
    5 KB (692 words) - 14:01, 23 May 2021
  • | SolubleOther = Soluble in [[acetone]], [[ethyl acetate]] and short alcohols<br>Insoluble in [[benzene]], [[chloroform]], [[toluene]], [[diethyl ether]] ...soluble in water, 209 g/100 ml at 25 °C. It is also soluble in low chain alcohols. For other solubilities refer to the info box. It is soluble in iso-butanol
    8 KB (1,080 words) - 09:06, 14 August 2023
  • ...water. It's smell is described as closer to acetone than other short chain alcohols like ethanol. It burns on contact with cuts (like ethanol) and it's widely [[Category:Alcohols]]
    8 KB (1,041 words) - 10:33, 30 July 2023
  • 8 KB (1,003 words) - 14:48, 18 November 2023
  • [[Category:Alcohols]] [[Category:Primary alcohols]]
    5 KB (552 words) - 14:42, 19 April 2020
  • ...a chromate ester as an intermediate, similar to other esters produced from alcohols. Decomposition of the ester forms a carbonyl group in the new structure, co ...tion is not inherently selective in producing aldehydes alone from primary alcohols. A work-around may be to drip Jones reagent into a large excess of the alco
    5 KB (879 words) - 18:55, 11 July 2019
  • ...grade products including KOH, NaOH, HCl<sub>(aq)</sub>, NH<sub>4</sub>OH, alcohols, glycols. ...d products, inclusing samples of various perfume essences (like ling chain alcohols).
    21 KB (3,057 words) - 21:32, 19 March 2024
  • ...yellow-orange powder that is nearly insoluble in water but soluble in many alcohols. This makes it especially useful for the production of pH testing strips, a
    5 KB (658 words) - 21:08, 19 July 2018
  • [[Category:Alcohols]]
    5 KB (560 words) - 13:55, 18 November 2023
  • ...d [[hydrochloric acid]]s, can be used to oxidize [[primary alcohol|primary alcohols]] to [[aldehyde]]s and [[secondary alcohol]]s to [[ketone]]s.
    7 KB (974 words) - 17:44, 30 November 2022
  • 9 KB (1,103 words) - 12:29, 25 June 2023
  • ...above 200 °C, in the presence of a tertiary or sterically bulk secondary alcohols, like [[tert-Butanol|t-butanol]] and [[menthol]]. The yield of this route i
    16 KB (2,327 words) - 18:19, 29 August 2021
  • 7 KB (831 words) - 17:39, 2 June 2021
  • *Ethers and long-chained alcohols must never be distilled to dryness, as they tend form explosive peroxides d ...luminium alloy will react with acids much faster, but will also react with alcohols and even water. Because of this phenomenon, avoid putting gallium on alumin
    48 KB (5,818 words) - 20:11, 13 March 2024
  • ...also soluble in liquid ammonia and pyridine. It is poorly soluble in most alcohols, like [[methanol]] and [[ethanol]].
    5 KB (609 words) - 18:43, 17 August 2020
  • ...at even very low concentrations. It is only very slightly soluble in lower alcohols and other organic solvents, but solubility increases slightly with the addi
    5 KB (539 words) - 22:20, 11 November 2020
  • [[Category:Alcohols]] [[Category:Tertiary alcohols]]
    5 KB (655 words) - 07:29, 14 February 2021
  • 5 KB (605 words) - 18:39, 3 October 2018
  • Zinc sulfate is a white hygroscopic solid. It is soluble in water and some alcohols. It forms three hydrates.
    5 KB (650 words) - 20:20, 10 February 2020
  • Phenol is weakly acidic, though still more acidic than aliphatic alcohols (about one million times more acidic), and at high pH gives the '''phenoxid
    10 KB (1,312 words) - 21:33, 5 March 2024
  • * Make brominated hydrocarbons from alcohols (useful in making grignards)
    5 KB (677 words) - 19:21, 20 June 2023
  • 5 KB (574 words) - 22:53, 22 May 2018
  • ...strong fishy-like. It is very soluble in water and organic solvents, like alcohols.
    8 KB (1,050 words) - 13:47, 26 August 2023
  • ...good solubility in water (73.9 g/100 ml at 20 °C), but is less soluble in alcohols and [[ethylene glycol]]. It melts at 66 °C (anhydrous) and 73.9 °C (nonah
    6 KB (690 words) - 17:03, 26 December 2018
  • It is a very potent oxidizer. It oxidizes primary alcohols to carboxylic acids, carboxylic acids to carbon dioxide and water, chlorate
    11 KB (1,555 words) - 17:28, 30 November 2022
  • 5 KB (517 words) - 21:17, 9 January 2022
  • As it is sensitive to moisture and alcohols, it's best to store it in a hermetically sealed container, a desiccator or
    6 KB (790 words) - 00:11, 11 December 2019
  • | SolubleOther = Slowly reacts with alcohols<br>Insoluble in [[acetone]], [[acetonitrile]], [[dichloromethane]]
    6 KB (717 words) - 16:43, 30 July 2023
  • [[Category:Alcohols]] [[Category:Sugar alcohols]]
    5 KB (624 words) - 17:51, 3 December 2021
  • 8 KB (1,057 words) - 08:26, 27 July 2019
  • | SolubleOther = Miscible with hydrocarbons, anhydrous alcohols<br>Insoluble in [[glycerol]]
    5 KB (546 words) - 15:21, 18 November 2023
  • [[Category:Alcohols]] [[Category:Sugar alcohols]]
    4 KB (431 words) - 19:31, 28 June 2017
  • ...[sucrose]]). It is soluble in water, but less so in organic solvents, like alcohols and [[acetone]]. ...countries. It is slightly less sweet than sucrose, but unlike other sugar alcohols it does not have a laxative effect at low doses for most people. Consuming
    5 KB (570 words) - 13:58, 16 April 2023
  • [[Category:Alcohols]]
    5 KB (617 words) - 16:15, 2 January 2022
  • | SolubleOther = Reacts with [[amine]]s, alkali<br> Slightly soluble in alcohols ...oiodic acid. The dissolution is exothermic. It is also slightly soluble in alcohols.
    7 KB (872 words) - 23:09, 28 March 2020
  • 6 KB (688 words) - 15:30, 24 October 2018
  • Symmetric ethers are commonly prepared via acid catalyzed dehydration of alcohols.
    1 KB (196 words) - 21:59, 1 December 2018
  • ...g/L at 20 °C), although it will form emulsions. It is however soluble in alcohols and ether It has a strong odor which is reminiscent of fruity candy and blu
    5 KB (542 words) - 21:21, 13 September 2020
  • Aluminium sulfide will react with alcohols at high temperature to give their respective thiols. such as: With [[methan
    6 KB (790 words) - 19:18, 19 July 2017
  • | SolubleOther = Insoluble in alcohols, halocarbons, hydrocarbons ...orless white hygroscopic solid, slightly soluble in water and insoluble in alcohols.
    6 KB (746 words) - 15:14, 18 November 2023
  • The same reaction also happens with alcohols, giving barium alkoxide.
    9 KB (1,241 words) - 21:55, 14 May 2018
  • ...ss.org/whisper/viewthread.php?tid=15171 Synthesis of longer chain tertiary alcohols]''
    16 KB (1,869 words) - 16:27, 13 March 2024
  • [[Category:Alcohols]]
    5 KB (656 words) - 08:55, 5 August 2021
  • Water is also a polar solvent, as are alcohols.
    3 KB (509 words) - 15:45, 10 March 2017
  • Many chemicals, such as [[ether]]s or secondary alcohols, tend to undergo autoxidation when in contact with air. Halogenated carbons ...c acid]] will serve as nourishment for mold or other biological organisms. Alcohols, like [[ethanol]], will not turn into their respective carboxylic acids (li
    20 KB (2,386 words) - 20:46, 1 March 2021
  • ...uble in water, but more soluble in various organic solvents, like ether or alcohols.
    7 KB (904 words) - 15:22, 10 July 2019
  • ...water, but very soluble in [[acetone]] and other ketones, as well as most alcohols and ethers. Its solubility in alcohol decreases as the alcohol weight incre
    6 KB (734 words) - 19:52, 31 August 2022
  • ...ulfate is a pinkish crystalline salt, soluble in water, as well as primary alcohols, though insoluble in aprotic solvents, such as [[benzene]] or [[diethyl eth
    6 KB (747 words) - 20:21, 20 March 2023
  • ...s.acs.org/doi/abs/10.1021/j150566a032</ref> It is also slightly soluble in alcohols, such as [[methanol]] and [[ethanol]].
    6 KB (773 words) - 17:47, 31 July 2023
  • 9 KB (1,198 words) - 20:39, 6 August 2023
  • [[Category:Alcohols]] [[Category:Secondary alcohols]]
    4 KB (506 words) - 18:40, 27 May 2023
  • 6 KB (757 words) - 20:55, 2 February 2020
  • | SolubleOther = Reacts with amines<br>Soluble in alcohols ...sh, due to traces of bromine. It is extremely soluble in water, as well as alcohols and other organic solvents. Hydrogen bromide has an unpleasant acrid smell.
    5 KB (620 words) - 20:59, 2 December 2018
  • ...s its decomposition. Thionyl chloride reacts with water, carboxylic acids, alcohols and all protic solvents. It is however miscible and soluble in most aprotic
    7 KB (931 words) - 21:18, 22 October 2022
  • ...ot be oxidized to an [[aldehyde]] or [[ketone]], like primary or secondary alcohols can. [[Category:Alcohols]]
    6 KB (674 words) - 19:08, 3 November 2023
  • Primary alcohols to carboxylic acids: Secondary alcohols to ketones:
    6 KB (750 words) - 20:21, 30 August 2023
  • ...luble in conc. sulfuric acid<br>Slightly soluble in acetates, [[acetone]], alcohols, amides, aq. acids, [[diethyl ether]]<br>Insoluble in [[ethanol]]
    5 KB (653 words) - 22:02, 5 November 2023
  • *Detect tertiary alcohols
    6 KB (670 words) - 20:53, 10 April 2020
  • | SolubleOther = Reacts with alcohols, carboxylic acids<br>Insoluble in common solvents ...lid powder, insoluble in all solvents. It reacts vigorously with water and alcohols. CaH<sub>2</sub> has a density of 1.70 g/cm<sup>3</sup>.
    4 KB (455 words) - 17:58, 13 January 2024
  • ...romic acid are used to oxidize primary alcohols to aldehydes and secondary alcohols to ketones.
    7 KB (974 words) - 19:39, 16 October 2022
  • | SolubleOther = Slightly soluble in alcohols<br>Insoluble in [[ester]]s, [[ether]]s, hydrocarbons, halocarbons
    5 KB (602 words) - 15:05, 18 November 2023
  • ...de is a deep red viscous liquid, which fumes in air. It reacts with water, alcohols, but soluble in chlorinated carbons and carboxylic acids.
    6 KB (808 words) - 20:08, 16 October 2022
  • | SolubleOther = Miscible with alcohols, ethers, ketones ...at soluble in water (25%) and miscible with other organic solvents such as alcohols and ethers. Methyl acetate has a melting point of −98 °C. Its boiling po
    5 KB (636 words) - 11:29, 5 May 2018
  • | SolubleOther = Reacts with alcohols<br>Soluble in [[benzene]], [[carbon disulfide]], [[hexane]], [[1,2-Dichloro Phosphorus triiodide will react with alcohols to form alkyl iodides:
    7 KB (863 words) - 19:36, 20 June 2023
  • ...htly soluble in [[acetic anhydride]], [[thionyl chloride]]<br>Insoluble in alcohols, alkanes, liq. [[sulfur dioxide]]
    8 KB (1,097 words) - 20:54, 30 July 2023
  • ...d ignites immediately on contact with air. It reacts violently with water, alcohols and acids. ...tmosphere or under inert solvent (like mineral oil or toluene). Long chain alcohols can be used to neutralize it, as the reaction proceeds slow.
    2 KB (307 words) - 21:20, 24 April 2020
  • ...ub>]], castor oil, kerosene, ligroin, [[nitrobenzene]], paraffins, terpene alcohols, [[toluene]], [[methyl salicylate|wintergreen oil]].<ref>Journal of the Ame
    6 KB (782 words) - 19:42, 12 February 2023
  • ...l. It is insoluble in water, but miscible with many organic solvents, like alcohols.
    5 KB (517 words) - 18:24, 31 August 2020
  • 6 KB (681 words) - 16:39, 1 March 2021
  • ...lowish hygroscopic solid, soluble in water and slightly soluble in primary alcohols, while insoluble in alkanes and chlorocarbons. It has a density of 2.168 g/
    8 KB (1,002 words) - 14:53, 18 November 2023
  • | SolubleOther = Reacts with acids<br>Insoluble in alcohols, [[benzene]], [[chloroform]], [[toluene]] ...icarbonate is a white hygroscopic solid, soluble in water but insoluble in alcohols and other organic solvents.
    5 KB (550 words) - 16:41, 3 July 2019
  • Alternatively, secondary alcohols having an alpha methyl group (such as [[isopropanol]]) can also be used, as
    2 KB (241 words) - 15:52, 30 May 2018
  • [https://www.youtube.com/watch?v=1SS3-D-Aqr4 Seperation of Ethanol(and alcohols in general) and Water with Salt]
    9 KB (1,320 words) - 09:45, 9 January 2022
  • ...ve/rhodium/chemistry/alkylbromides.html Preparation of Alkyl Bromides From Alcohols]''' ...istry/mesylates.html Synthesis of Methanesulfonate Esters (Mesylates) From Alcohols]'''
    6 KB (941 words) - 16:51, 27 September 2016
  • | SolubleOther = Soluble in acids<br>Slightly soluble in alcohols
    4 KB (476 words) - 19:36, 22 August 2020
  • ...ly soluble in water, but more soluble in organic solvents, such as primary alcohols and acetone.
    4 KB (421 words) - 20:22, 16 October 2022
  • Oxidation of primary alcohols, such as methanol or ethanol with [[potassium permanganate]] in the presenc ...re the side products from the [[haloform reaction]]. The following ketones/alcohols will give the following carboxylates:
    4 KB (526 words) - 13:34, 31 December 2021
  • | SolubleOther = Reacts with alcohols, aldehydes, amines<br>Miscible with glacial [[acetic acid]], [[acetone]], [ Acetyl chloride will react with alcohols to yield esters and [[hydrogen chloride]]:
    7 KB (949 words) - 22:24, 8 January 2024
  • 9 KB (1,123 words) - 21:14, 22 October 2022
  • ...colorless solid, which hydrolyzes in contact with water, but is soluble in alcohols.
    6 KB (759 words) - 20:55, 10 October 2019
  • ...a reducing agent for reducing ketones and aldehydes to their corresponding alcohols. It has the chemical formula '''C<sub>9</sub>H<sub>21</sub>O<sub>3</sub>Al' Aluminium isopropoxide is a colorless solid, slightly soluble in alcohols, but more soluble in [[tetrahydrofuran|THF]] and [[carbon disulfide]]. It h
    6 KB (660 words) - 17:58, 8 August 2018
  • | SolubleOther = Reacts with alcohols, carboxylic acids<br>Soluble in [[benzene]], [[carbon disulfide]], [[carbon ...ntachloride is a fuming white solid, which reacts violently with water and alcohols. It is soluble in many organic solvents such as [[benzene]], chlorinated ca
    8 KB (1,001 words) - 21:15, 22 October 2022
  • | SolubleOther = Reacts with alcohols, carboxylic acids<br>Soluble in benzoyl chloride, [[bromine]], bromoacetic
    6 KB (750 words) - 09:43, 15 August 2022
  • Zinc nitrate is an odorless hygroscopic solid, soluble in water and alcohols.
    5 KB (602 words) - 18:13, 14 September 2018
  • ...olid, with a slight vinegar-like smell. It is soluble in water and primary alcohols.
    4 KB (478 words) - 18:05, 24 December 2016
  • 6 KB (765 words) - 20:59, 2 December 2018
  • | SolubleOther = Reacts with alcohols, carboxylic acids<br>Soluble in AsCl<sub>3</sub>, [[bromine]], liq. [[Hydro
    5 KB (599 words) - 20:58, 2 December 2018
  • 5 KB (508 words) - 15:12, 31 December 2018
  • 12 KB (1,637 words) - 21:45, 25 July 2022
  • ...roxide and volatile flammable solvents that do not attack plastic, such as alcohols, are generally stored in PE bottles.
    7 KB (1,092 words) - 20:41, 2 October 2022
  • ...ive oxide layer, which makes the metal susceptible to the action of water, alcohols. This property is exploited when synthesizing [[aluminium isopropoxide]].
    6 KB (705 words) - 22:11, 28 March 2020
  • Ammonium dichromate is a red-orange solid, soluble in water and alcohols, but less so in other solvents.
    5 KB (576 words) - 19:12, 9 November 2018
  • | SolubleOther = Reacts with alcohols, [[carboxylic acid]]s, esters, halogens, mineral acids<br>Insoluble in [[et Reaction with alcohols gives their corresponding alkoxides.
    5 KB (655 words) - 19:10, 6 February 2020
  • 4 KB (466 words) - 20:27, 21 October 2022
  • 5 KB (564 words) - 09:42, 25 June 2023
  • ...[Jones oxidation]] to oxidize primary alcohols to aldehydes, and secondary alcohols to ketones. Sodium dichromate is an orange solid, hygroscopic and soluble in water and alcohols.
    5 KB (658 words) - 21:38, 23 May 2019
  • ...lk/viewthread.php?tid=65067 Niacin Chlorochromate (NCC??) for oxidation of alcohols]
    5 KB (554 words) - 21:54, 15 March 2021
  • ...thyl citrate is an oily liquid, poorly soluble in water, but miscible with alcohols.
    4 KB (403 words) - 20:23, 9 January 2017
  • ...h slowly hydrolyzes in water and miscible with many organic solvents, like alcohols.
    4 KB (427 words) - 21:37, 21 January 2020
  • | SolubleOther = Dissolves and slowly reacts with alcohols, amines<br>Soluble in [[acetone]], [[benzene]]<br>Slightly soluble in [[car
    7 KB (915 words) - 13:19, 29 August 2020
  • ...f> It is soluble in water, but more soluble in some organic solvents, like alcohols and ethers.
    7 KB (863 words) - 15:17, 30 July 2023
  • Tartaric acid is a crystalline colorless solid, soluble in water, acids and alcohols, but insoluble in hydrocarbons and halocarbons.
    7 KB (882 words) - 20:02, 14 January 2020
  • ...ightly soluble in [[Dimethyl sulfoxide|DMSO]], [[ethanol]]<br>Insoluble in alcohols, [[dichloromethane]], [[dimethylformamide]], [[tetrahydrofuran]]<ref>https: [[Category:Alcohols]]
    5 KB (533 words) - 21:41, 27 February 2021
  • *Make sugar alcohols from various sugar (ex: [[sorbitol]] from [[sucrose]])
    2 KB (346 words) - 16:39, 6 August 2017
  • 4 KB (498 words) - 21:51, 18 November 2019
  • | SolubleOther = Reacts with acids<br>Insoluble in [[acetone]], alcohols, [[ammonia]], ethers,
    4 KB (528 words) - 21:26, 16 October 2022
  • ...cannot be sealed completely. As such, only certain types of solvents, like alcohols, ketones, esters and ethers are generally employed.
    2 KB (335 words) - 18:43, 25 October 2020
  • *Other secondary alcohols
    13 KB (1,730 words) - 14:06, 9 August 2023
  • ...dioxide]] from air. It can form strongly alkaline solutions with water and alcohols. Aqueous solutions with a concentration of 20% have a pH of 13.5 at 25 °C.
    7 KB (902 words) - 19:02, 27 March 2022
  • 5 KB (567 words) - 16:33, 12 June 2018
  • Like most higher-chain alcohols, n-pentanol has a high flash point, meaning it has low flammability. [[Category:Alcohols]]
    5 KB (605 words) - 20:50, 27 July 2022
  • ''tert''-Amyl alcohol, like all tertiary alcohols, is not readily oxidized. Due to the high stability of the tert-amyl cation ...somewhat soluble in water, but miscible with other organic solvents, like alcohols and halocarbons.
    5 KB (564 words) - 21:00, 12 September 2019
  • ...partially dissolve both components, as AN is slightly soluble in low-chain alcohols, while most FOs are either soluble or miscible with them. AN/FO has a sligh
    5 KB (752 words) - 16:50, 2 July 2019
  • ...ntage), which is slightly soluble in water and more soluble in lower-chain alcohols. It is slightly hygroscopic, but NM's poor solubility in water limits this
    5 KB (687 words) - 20:19, 1 October 2021
  • While the exact mechanism is still debated, it is known that no alcohols are formed as intermediates, as OH groups cannot be reduced via this method
    2 KB (260 words) - 21:07, 29 July 2017
  • 5 KB (631 words) - 01:20, 30 August 2020
  • ...is a colorless crystalline solid, which dissolves in water. Like all sugar alcohols, it is insoluble in hydrocarbons. [[Category:Alcohols]]
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  • [[Category:Alcohols]] [[Category:Sugar alcohols]]
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  • It is sometimes available as sweetener, though not as common as other sugar alcohols. ...t's not commonly used as sweetener as it's more expensive than other sugar alcohols.
    4 KB (386 words) - 17:33, 21 July 2019
  • ...t's not commonly used as sweetener as it's more expensive than other sugar alcohols. [[Category:Alcohols]]
    4 KB (491 words) - 17:35, 21 October 2018
  • ...t's not commonly used as sweetener as it's more expensive than other sugar alcohols. [[Category:Alcohols]]
    3 KB (290 words) - 13:31, 6 August 2017
  • The Grignard reaction is useful for obtaining tertiaty alcohols.
    1 KB (202 words) - 21:10, 30 November 2018
  • Organometallic reagents are used in [[Grignard reaction]]s to obtain various alcohols, like [[tert-Butanol|tert-butanol]] from [[acetone]]. ...ding them in a non-polar solvent, like [[toluene]], where small amounts of alcohols are added to safely neutralize the Grignard reagent. This procedure must be
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  • Lithium borohydride is a white solid, which reacts with water and alcohols, but it's soluble in ethers.
    5 KB (558 words) - 21:28, 9 September 2023
  • ...b>4</sub> has been shown to reduce carboxylic acids to their corresponding alcohols. [[Tetrahydrofuran]] is often used as solvent in this case.<ref>https://pub Sodium borohydride is a white solid, which reacts with water and alcohols, though the reaction is fairly slow. Complete decomposition in excess [[met
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  • [[Category:Alcohols]] [[Category:Sugar alcohols]]
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  • Aldehydes can be easily prepared through the [[Jones oxidation]] of primary alcohols, which consists of [[chromium trioxide]] or [[potassium dichromate]] dissol Aldehydes can also be produced by oxidizing primary alcohols through near red hot copper. This method is simple enough that it can be us
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  • Ketones can be easily prepared through the [[Jones oxidation]] of secondary alcohols, using [[chromium trioxide]] or [[potassium dichromate]] dissolved in dilut *[http://www.sciencemadness.org/talk/viewthread.php?tid=65314 Ketones to Alcohols?]
    3 KB (428 words) - 22:37, 10 June 2018
  • ...nd [[methyl acetate]], slightly soluble in primary and secondary low-chain alcohols, acetic acid and insoluble in 25% aq. [[ammonia]], [[formaldehyde]] 37% and
    5 KB (529 words) - 16:18, 26 November 2019
  • ...osphate is a colorless crystalline solid, soluble in water, but less so in alcohols. It is odorless.
    4 KB (455 words) - 21:45, 5 June 2018
  • [[Category:Alcohols]] [[Category:Primary alcohols]]
    5 KB (621 words) - 10:50, 9 September 2023
  • ...used for the introduction of the benzyl protecting group in reaction with alcohols, yielding the corresponding benzyl ether, carboxylic acids, and benzyl este
    8 KB (1,110 words) - 21:27, 7 November 2021
  • 6 KB (656 words) - 18:03, 1 March 2021
  • 3 KB (541 words) - 19:35, 19 April 2019
  • 5 KB (554 words) - 23:31, 20 March 2020
  • 4 KB (524 words) - 16:18, 14 April 2020
  • ...her solvents like [[acetone]], [[benzene]], [[dimethylformamide]], primary alcohols, hydrocarbons. Gelatine has a density between 1.3-1.4 g/cm<sup>3</sup>.<ref
    3 KB (401 words) - 15:21, 18 November 2023
  • ...ms of reactive metals, like alkali metals will violently react with water, alcohols and may ignite in air.
    7 KB (1,009 words) - 22:21, 15 September 2022
  • 4 KB (440 words) - 20:49, 2 February 2020
  • | SolubleOther = Insoluble in alcohols, ether
    5 KB (622 words) - 20:32, 1 November 2020
  • ...ent smell. It dissolves extremely exothermically in water, and reacts with alcohols. It is insoluble in non-polar solvents, like hydrocarbons and halocarbons.
    5 KB (725 words) - 22:50, 20 January 2020
  • | SolubleOther = Reacts with amines<br>Soluble in alcohols (reacts)<br>Insoluble in ether
    5 KB (570 words) - 00:22, 29 March 2020
  • ...with density of 1.73 g/cm<sup>3</sup>, insoluble in water, but soluble in alcohols and ether.
    5 KB (555 words) - 19:23, 13 August 2018
  • ...eOther = Reacts with acids, aq. [[ammonia|NH<sub>3</sub>]]<br>Insoluble in alcohols, ethers, halocarbons, hydrocarbons
    5 KB (541 words) - 08:22, 5 August 2021
  • ...://www.sciencemadness.org/talk/viewthread.php?tid=12942 dehydrating higher alcohols with bisulfate] .../www.sciencemadness.org/talk/viewthread.php?tid=63170 Dehydration of sugar alcohols]
    2 KB (202 words) - 18:43, 19 July 2019
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  • | SolubleOther = Miscible with alcohols, carboxylic acids<br>Soluble in ether
    5 KB (621 words) - 16:36, 28 August 2018
  • ...viscous colorless liquid, with an ammoniacal odor, miscible with water and alcohols. [[Category:Alcohols]]
    6 KB (641 words) - 22:13, 20 January 2020
  • '''Sugar alcohols''' (also called '''polyhydric alcohols''', '''polyalcohols''', '''polyols''', '''alditols''' or '''glycitols''') a ==Common sugar alcohols==
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  • The compounds can be hydrolyzed to various long chain alcohols.
    5 KB (563 words) - 09:16, 25 June 2023
  • ...can be further dehydrated to yield nitroalkenes, nitroketones or β-amino alcohols, process known as [[nitroaldol reaction]] (or Henry reaction).
    7 KB (850 words) - 22:48, 20 January 2020
  • | SolubleOther = Reacts with alcohols, acids, [[bromine]], [[phenol]]<br>Insoluble in liq. [[ammonia]], organic s
    4 KB (445 words) - 20:32, 13 March 2024
  • Upon heating sulfamic acid will react with alcohols to form the corresponding organosulfates.
    7 KB (910 words) - 12:58, 18 November 2023
  • ...luble in organic solvents than longer chain alkoxides, long chain tertiary alcohols are the best for this reaction. ...tps://www.youtube.com/watch?v=PxPjBz_8S3c</ref> Different isomers of bulky alcohols don't have any effect of the reaction time and yield.<ref>https://www.youtu
    18 KB (2,804 words) - 20:34, 17 September 2022
  • ...reason, KF reagents are typically made as alcoholic solutions. Long-chain alcohols form the intermediate alkyl sulfite less readily, so [[methanol]] is common
    10 KB (1,556 words) - 18:24, 17 April 2019
  • | SolubleOther = Miscible with alcohols [[Category:Alcohols]]
    3 KB (357 words) - 22:40, 20 January 2020
  • | SolubleOther = Reacts with alcohols, aldehydes, ketones
    4 KB (415 words) - 17:34, 2 June 2021
  • Examples of primary alcohols include: [[methanol]], [[ethanol]], [[propanol]], [[butanol]] and [[pentano Primary alcohols can be oxidized to aldehydes or carboxylic acids.
    427 B (50 words) - 20:55, 22 March 2019
  • Examples of secondary alcohols: [[isopropanol]], [[sec-Butanol|''sec''-butanol]]. Secondary alcohols can be oxidized to [[ketone]]s.
    389 B (44 words) - 21:08, 22 March 2019
  • Examples of primary alcohols include: [[chlorobutanol]], [[tert-Amyl alcohol|''tert''-amyl alcohol]], [[ Tertiary alcohols cannot be oxidized like primary or secondary alcohols.
    464 B (51 words) - 21:14, 22 March 2019
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  • | SolubleOther = Reacts with alcohols, amines, [[carboxylic acid]]s ...loride behaves similarly to other [[acyl chloride]]s in that reacting with alcohols produces the corresponding [[ester]]. Unusually, however, reaction with wat
    4 KB (503 words) - 21:47, 11 October 2022
  • [[Category:Alcohols]] [[Category:Secondary alcohols]]
    4 KB (356 words) - 23:50, 24 March 2019
  • Bromoacetic acid is a near-colorless solid, very soluble in water and alcohols.
    4 KB (433 words) - 19:30, 18 June 2019
  • ...]] is produced. Grignard reagents add to propylene oxide to give secondary alcohols.
    4 KB (481 words) - 19:59, 21 January 2020
  • ...d an [[aldehyde]] or [[ketone]] in the presence of a base to form β-nitro alcohols. It is nearly analogous to the aldol reaction that had been discovered 23 y
    2 KB (269 words) - 21:22, 10 August 2020
  • ...r name, they are not nitro compounds, but rather nitrate esters or various alcohols/polyols, and the name "nitro" comes from the old designation of the prepara
    6 KB (839 words) - 21:28, 26 October 2020
  • | SolubleOther = Reacts with alcohols
    4 KB (401 words) - 18:57, 12 March 2023
  • ...er, essential oils, hydrocarbon solvents, etc. While it's legal to distill alcohols like methanol, propanol, iropropanol, butanol, etc., distillation of ethano ...acetic, citric, tartaric acids and their salts, sodium hydroxide, various alcohols and esters, that not only encountered as OTC products but are also disposed
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  • 5 KB (570 words) - 17:26, 27 May 2023
  • Difluoroacetic acid is a colorless liquid, miscible with water and alcohols.
    4 KB (366 words) - 17:27, 27 May 2023
  • 4 KB (485 words) - 20:52, 2 February 2020
  • 5 KB (607 words) - 19:45, 27 July 2022
  • ...enated solvents ([[chloroform]] e.g.), [[dioxane]] and somewhat soluble in alcohols.
    5 KB (576 words) - 15:13, 27 May 2023
  • ...oform]], [[diethyl ether]], [[tetrahydrofuran|THF]]<br>Slightly soluble in alcohols
    4 KB (456 words) - 14:18, 6 October 2019
  • Thiourea dioxide can be used to reduce ketones to secondary alcohols.<ref>https://www.sciencedirect.com/science/article/pii/S0040403901843203</r
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  • | SolubleOther = Miscible with alcohols, esters, ethers, halocarbons
    5 KB (511 words) - 21:21, 15 September 2022
  • 5 KB (531 words) - 20:48, 3 January 2020
  • | SolubleOther = Slightly soluble in alcohols
    4 KB (424 words) - 22:56, 3 January 2020
  • ...>2</sub>OH'''. Allyl alcohol is the smallest representative of the allylic alcohols Allyl alcohol is more toxic than related simple alcohols. Its threshold limit value (TLV) is 2 ppm. It is also a lachrymator.
    6 KB (728 words) - 20:21, 15 September 2022
  • ...n it, but miscible with ethers, esters, halocarbons. While it dissolves in alcohols, it will slowly react with them as well.
    5 KB (582 words) - 15:51, 2 February 2020
  • [[Category:Alcohols]]
    5 KB (578 words) - 19:06, 2 February 2020
  • [[Category:Alcohols]] [[Category:Secondary alcohols]]
    5 KB (526 words) - 19:03, 15 February 2020
  • [[Category:Alcohols]] [[Category:Amino alcohols]]
    5 KB (580 words) - 20:34, 5 December 2020
  • ...e in most organic solvents, although it shows some solubility in low-chain alcohols, which increases with temperature.
    7 KB (890 words) - 20:09, 24 October 2023
  • | SolubleOther = Reacts with alcohols<br>Soluble in [[acetic acid]], [[acetone]], [[arsenic trichloride]], [[brom
    6 KB (727 words) - 17:06, 29 February 2020
  • [[Category:Alcohols]] [[Category:Secondary alcohols]]
    6 KB (764 words) - 18:04, 5 March 2024
  • ...tly soluble in dil. [[hydrochloric acid]], aq. [[ammonia]]<br>Insoluble in alcohols, carboxylic acids, hydrocarbons
    5 KB (629 words) - 00:22, 26 August 2020
  • | SolubleOther = Insoluble in alcohols, [[hydrochloric acid]], hydrocarbons
    6 KB (720 words) - 23:21, 28 March 2020
  • 6 KB (673 words) - 21:59, 14 June 2020
  • 4 KB (491 words) - 11:35, 28 December 2020
  • ...y, beeswax consists mainly of esters of fatty acids and various long-chain alcohols. ...>COOH, the two principal constituents, being 6:1. Various other long-chain alcohols are present, as well as a few percentages of various other side biological
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  • [[Category:Alcohols]] [[Category:Tertiary alcohols]]
    5 KB (604 words) - 22:20, 26 October 2020
  • ...anth JV, Periasamy M (1991). "Selective Reduction of Carboxylic Acids into Alcohols Using NaBH and I2". Journal of Organic Chemistry. 56: 5964–5965</ref> [[Category:Alcohols]]
    6 KB (682 words) - 21:25, 1 October 2023
  • ...ion as a suitable nucleophile. However, as ethers show similar basicity as alcohols (pKa of approximately 16), the equilibrium of protonation lies on the side
    3 KB (518 words) - 16:20, 6 June 2020
  • 6 KB (753 words) - 22:08, 26 October 2020
  • ...slightly miscible with water, but more soluble in organic solvents such as alcohols and ketones. PLX has an average density of 1.13 g/cm<sup>3</sup> at standar
    3 KB (442 words) - 17:30, 12 July 2020
  • 7 KB (855 words) - 19:34, 27 September 2020
  • ...turquoise hygroscopic solid. It is soluble in water and low-weight primary alcohols.
    6 KB (687 words) - 16:07, 2 January 2022
  • Nitrosylsulfuric acid is a pale yellowish solid, that reacts with water and alcohols. It is very soluble in conc. sulfuric acid and fuming nitric acid. The comp
    6 KB (736 words) - 19:21, 22 March 2021
  • ...though air oxidation will give it a beige tint, which is soluble in water, alcohols and ether.
    5 KB (542 words) - 00:10, 15 November 2020
  • | SolubleOther = Soluble in [[acetonitrile]], alcohols, [[Dimethyl sulfoxide|DMSO]]<br>Slightly soluble in glacial [[acetic acid]] ...chlorate is a hygroscopic colorless solid, soluble in water and low weight alcohols.
    6 KB (650 words) - 22:29, 15 August 2022
  • | SolubleOther = Reacts with alcohols, bases, carboxylic acids, esters, mineral acids<br>Miscible with [[benzene]
    7 KB (843 words) - 22:43, 17 November 2020
  • 6 KB (709 words) - 21:06, 15 September 2022
  • | SolubleOther = Soluble in alcohols ...m nitrate is a white hygroscopic volatile solid, very soluble in water and alcohols.
    4 KB (471 words) - 21:10, 29 November 2020
  • [[Category:Alcohols]] [[Category:Amino alcohols]]
    5 KB (544 words) - 23:22, 5 December 2020
  • ...idine hydrochloride is a hygroscopic colorless solid, soluble in water and alcohols.
    6 KB (730 words) - 19:47, 28 December 2023
  • ...rless solid, that slowly turns brownish in air. It is soluble in water and alcohols.
    5 KB (509 words) - 12:12, 29 December 2020
  • [[Category:Alcohols]]
    4 KB (486 words) - 14:04, 29 December 2020
  • | SolubleOther = Reacts with alcohols<br>Soluble in [[acetonitrile]], conc. [[sulfuric acid]]<br>Sparingly solubl
    7 KB (765 words) - 19:25, 31 December 2020
  • 6 KB (732 words) - 18:19, 15 March 2022
  • | SolubleOther = Soluble in alcohols
    4 KB (487 words) - 15:30, 25 May 2021
  • | SolubleOther = Reacts with alcohols<br>Miscible with [[carbon tetrachloride]], [[chloroform]], [[diethyl ether] ...r. Impure samples may appear yellowish or cloudy. It reacts with water and alcohols, but it's miscible with ethers.
    7 KB (933 words) - 20:35, 25 May 2021
  • | SolubleOther = Miscible with alcohols, ethers, halocarbons, hydrocarbons
    5 KB (626 words) - 20:47, 16 May 2021
  • | SolubleOther = Insoluble in alcohols
    5 KB (614 words) - 18:28, 26 October 2022
  • Lithium nitrite is a colorless hygroscopic solid, soluble in water and alcohols.
    5 KB (584 words) - 22:34, 7 November 2021
  • | SolubleOther = Reacts with alcohols, amines, bases<br>Miscible with [[benzene]], [[carbon disulfide]], ethers, Benzoyl chloride reacts with alcohols to give the corresponding esters. Similarly, it reacts with amines to give
    6 KB (662 words) - 10:16, 7 July 2022
  • | SolubleOther = Insoluble in alcohols
    4 KB (382 words) - 20:37, 13 March 2024
  • 5 KB (491 words) - 22:14, 8 November 2021
  • ...olorless crystalline solid, soluble in water, and slightly less soluble in alcohols.
    5 KB (644 words) - 23:48, 13 November 2021
  • 5 KB (526 words) - 21:53, 17 September 2022
  • [[Category:Alcohols]]
    4 KB (462 words) - 20:47, 14 November 2021
  • 6 KB (714 words) - 15:37, 17 August 2022
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  • ...ence of [[acetic acid|acetic]] or [[phosphoric acid]] at room temperature. Alcohols like [[methanol]] or [[ethanol]] can be used as the reaction media, as they
    7 KB (821 words) - 22:03, 29 December 2021
  • 4 KB (420 words) - 14:32, 31 December 2021
  • | SolubleOther = Soluble in alcohols
    6 KB (755 words) - 16:43, 31 December 2021
  • | SolubleOther = Reacts with alcohols, amines<br>Soluble in [[benzene]], [[chloroform]], [[diethyl ether]], [[Tet Tosyl chloride converts alcohols into the corresponding toluenesulfonate esters or tosylates:
    5 KB (629 words) - 19:54, 15 September 2022
  • | SolubleOther = Reacts with acids<br>Miscible with [[acetone]], alcohols, [[benzene]], [[diethyl ether]], [[Tetrahydrofuran|THF]]
    4 KB (402 words) - 22:43, 1 September 2022
  • It reacts similarly with alcohols, but yields borate esters instead of free acid. Reaction with [[methanol]] Diborane readily reduces carboxylic acids to the corresponding alcohols, whereas ketones react only sluggishly.
    6 KB (837 words) - 21:16, 2 September 2022
  • | SolubleOther = Reacts with alcohols<br>Miscible with liq. [[Sulfur dioxide|SO<sub>2</sub>]]<br>Soluble in [[Car Alcohols behave analogously giving the borate esters, e.g. [[trimethyl borate]].
    5 KB (597 words) - 21:11, 22 October 2022
  • Organic compounds, such as ethers, secondary alcohols or certain unsaturated hydrocarbons will produce unstable peroxides upon co
    4 KB (526 words) - 12:51, 25 August 2023
  • [[Category:Alcohols]] [[Category:Primary alcohols]]
    4 KB (402 words) - 22:46, 30 July 2023
  • ...Verley reduction can be performed on prochiral ketones leading to chiral alcohols. The three main ways to achieve the asymmetric reduction is by use of a chi
    1 KB (196 words) - 15:55, 25 July 2023
  • Saline water is not miscible with many alcohols or other water miscible solvents, property which can be used to separate th
    3 KB (382 words) - 16:47, 25 July 2023
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  • | SolubleOther = Somewhat soluble in alcohols<br>Poorly soluble in [[acetone]]<br>Insoluble in [[chloroform]], [[ether]]s
    11 KB (1,497 words) - 18:41, 28 March 2024
  • | SolubleOther = Reacts with alcohols, acids<ref>Comey A. M., Hahn D. A. A dictionary of Chemical Solubilities In ...this compound: One involves slow addition of organic esters or long-chain alcohols, which are diluted in an inert solvent (like ether), under inert gas and di
    8 KB (1,004 words) - 14:42, 16 August 2023
  • ...s mechanism, sodium-ethanol mixtures will also reduce ketones to secondary alcohols. ...ium aluminium hydride]] is the choice reducing agent in reducing esters to alcohols, for the hobby chemist, this reagent is expensive and hard to come by. As s
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  • ...which is hygroscopic and a powerful lachrymator. It reacts with water and alcohols and protic solvents, but dissolves in halocarbons.
    8 KB (1,050 words) - 20:53, 5 November 2023
  • ...t readily and violently reacts with water, and some organic solvents, like alcohols, esters and ammonia or amines. In a perfectly dry environment, the compound
    5 KB (627 words) - 20:30, 8 November 2023
  • 4 KB (391 words) - 22:06, 24 December 2023
  • ...It is highly soluble in water as well as many other organic solvents, like alcohols, aromatics and ethers.
    6 KB (706 words) - 22:03, 25 December 2023
  • [[Category:Alcohols]] [[Category:Secondary alcohols]]
    5 KB (596 words) - 23:32, 27 December 2023
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  • ...ellow is a yellowish solid, almost insoluble in water, but more soluble in alcohols.
    5 KB (524 words) - 21:40, 28 December 2023
  • Metformin is a colorless solid, soluble in water and alcohols.
    4 KB (489 words) - 22:13, 29 December 2023
  • [[Category:Alcohols]] [[Category:Primary alcohols]]
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