Ads
related to: organic chemistry 2 practice problems free
Search results
Results from the WOW.Com Content Network
2 Organic chemistry problems. 3 Inorganic chemistry problems. 4 Biochemistry problems. 5 See also. 6 References. 7 External links. Toggle the table of contents.
Retrosynthetic analysis is a technique for solving problems in the planning of organic syntheses. This is achieved by transforming a target molecule into simpler precursor structures regardless of any potential reactivity/interaction with reagents. Each precursor material is examined using the same method.
One problem addressed by mixed cuprates is the economical use of the alkyl group. Thus, in some applications, the mixed cuprate with the formula Li 2 [Cu(2-thienyl)(CN)R] is prepared by combining thienyllithium and cuprous cyanide followed by the organic group to be transferred. In this higher order mixed cuprate, both the cyanide and thienyl ...
In organic chemistry, the oxymercuration reaction is an electrophilic addition reaction that transforms an alkene (R 2 C=CR 2) into a neutral alcohol. In oxymercuration, the alkene reacts with mercuric acetate (AcO−Hg−OAc) in aqueous solution to yield the addition of an acetoxymercury (−HgOAc) group and a hydroxy (−OH) group across the ...
The specific problem is: uneven quality of sourcing—substantially primary (and not full) sources—reflecting editorial decisions to include/exclude examples, decisions that, i, constitute original research, and ii, that are unfortunately not scholarly and up to date. Please help improve this article if you can.
Organic chemistry is a subdiscipline within chemistry involving the scientific study of the structure, properties, and reactions of organic compounds and organic materials, i.e., matter in its various forms that contain carbon atoms. [1]
In organic chemistry, dehalogenation is a set of chemical reactions that involve the cleavage of carbon-halogen bonds; as such, it is the inverse reaction of halogenation. Dehalogenations come in many varieties, including defluorination (removal of fluorine ), dechlorination (removal of chlorine ), debromination (removal of bromine ), and ...
Arrow pushing or electron pushing is a technique used to describe the progression of organic chemistry reaction mechanisms. [1] It was first developed by Sir Robert Robinson.In using arrow pushing, "curved arrows" or "curly arrows" are drawn on the structural formulae of reactants in a chemical equation to show the reaction mechanism.
Ads
related to: organic chemistry 2 practice problems free