Search results
Results from the WOW.Com Content Network
The page provides a comprehensive list of isomers of dodecane, including their chemical structures and properties.
The parent isoindole was prepared by flash vacuum pyrolysis of an N-substituted isoindoline. [5] N-Substituted isoindoles, which are easier to handle, can be prepared by dehydration of isoindoline-N-oxides. They also arise by myriad other methods, e.g., starting from xylylene dibromide (C 6 H 4 (CH 2 Br) 2).
This page was last edited on 18 November 2024, at 00:50 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
3-Ethyl-2-methyldecane; 3-Ethyl-3-methyldecane; 3-Ethyl-4-methyldecane; 3-Ethyl-5-methyldecane; 3-Ethyl-6-methyldecane; 3-Ethyl-7-methyldecane; 3-Ethyl-8-methyldecane
Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file
Diiodomethane is a reagent for installing the CH 2 group. In the Simmons–Smith reaction, it is a source of methylene. [4] In fact the Simmons–Smith reaction does not produce free carbene but proceeds via Zn-CH 2 I intermediates. Diiodomethane is also a source of the equivalent of CH 2+ 2. The synthesis of Fe 2 (CH 2)(CO) 8 illustrates this ...
4-Iodophenol (p-iodophenol) is an aromatic organic compound. A colorless solid, it is one of three monoiodophenols. 4-Iodophenol undergoes a variety of coupling reactions in which the iodine substituent is replaced by a new carbon group para to the hydroxy group of the phenol . [ 3 ]
The preparation of 1,1-diiodoethane from gem-dihaloalkanes [3] To be specific, mix 0.4 mol (~39.6 g) of 1,1-dichloroethane with 1.2 mol (~187 g) of ethyl iodide, and ~2.0 g of aluminium chloride. Heat for three hours using steam bath. Then, wash the mixture with H 2 O and NaHSO 3 respectively, and dry with MgSO 4. By boiling at 76-76 °C and 25 ...