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1-nitropropane is produced industrially by the reaction of propane and nitric acid. This reaction forms four nitroalkanes: nitromethane, nitroethane, 1-nitropropane, and 2-nitropropane. 1-nitropropane is also a byproduct of the process for making 2-nitropropane, which is done by vapour phase nitration of propane.
Nitro compound hydrogenation. The α-carbon of nitroalkanes is somewhat acidic. The pK a values of nitromethane and 2-nitropropane are respectively 17.2 and 16.9 in dimethyl sulfoxide (DMSO) solution, suggesting an aqueous pK a of around 11. [22] In other words, these carbon acids can be deprotonated in aqueous solution.
Nitropropane may refer to: 1-Nitropropane; 2-Nitropropane This page was last edited on 16 May 2022, at 02:06 (UTC). Text is available under the Creative Commons ...
Nitroethane is an organic compound having the chemical formula C 2 H 5 NO 2. Similar in many regards to nitromethane, nitroethane is an oily liquid at standard temperature and pressure. Pure nitroethane is colorless and has a fruity odor.
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1,4-Dioxane (/ d aɪ ˈ ɒ k s eɪ n /) is a heterocyclic organic compound, classified as an ether. It is a colorless liquid with a faint sweet odor similar to that of diethyl ether . The compound is often called simply dioxane because the other dioxane isomers ( 1,2- and 1,3- ) are rarely encountered.
In organic chemistry, the Hass–Bender oxidation (also called the Hass–Bender carbonyl synthesis [1]) is an organic oxidation reaction that converts benzyl halides into benzaldehydes using the sodium salt of 2-nitropropane as the oxidant. [2] This name reaction is named for Henry B. Hass and Myron L. Bender, who first reported it in 1949. [3]
Dioxane may refer to the following chemical compounds: 1,2-dioxane; 1,3-dioxane; 1,4-dioxane This page was last edited on 13 October ...