Examples of 'carbonyls' in a sentence
Meaning of "carbonyls"
Carbonyl is a chemical group consisting of a carbon atom double-bonded to an oxygen atom. It is commonly found in organic compounds
Show more definitions
- plural of carbonyl
How to use "carbonyls" in a sentence
Basic
Advanced
carbonyls
The carbonyls have been omitted for clarity.
However it has an effect on the carbon in α of carbonyls.
Metal carbonyls are used in several industrial processes.
Coupling between carbonyls and oxyamines.
Carbonyls also may be alkylated by enolates as in aldol reactions.
Preferably both carbonyls are bonded to the same ring.
Carbonyls are discussed in more detail elsewhere in this chapter.
Preferably the chain is composed of hydrocarbons and carbonyls.
Cobalt carbonyls or hydrocarbonyls can also be used.
Pyridoxal acts to remove carbonyls in blood.
Cobalt carbonyls or hydrocarbonyls can also be employed.
Process for removing metal carbonyls from gaseous streams.
Metal carbonyls are used in a number of industrially important carbonylation reactions.
The gas may contain metal carbonyls in any concentration.
Carbonyls have been shown to interact favorably with carbon dioxide.
See also
They also add to carbonyls and other oxidative groups.
They arise in general by the condensation of unsaturated metal carbonyls.
The resulting carbonyls are then thermally decomposed.
Another important reaction catalyzed by metal carbonyls is the hydrocarboxylation.
Most metal carbonyls do undergo halogenation.
An important technique for characterizing metal carbonyls is infrared spectroscopy.
Many organic carbonyls undergo decarbonylation.
Infrared spectroscopy of metal carbonyls.
Transition metal carbonyls include dimanganese decacarbonyl.
Potassium in graphite shows distinctive reducing properties towards carbonyls.
Most metal carbonyls can be halogenated.
Reaction of nucleophiles with carbonyls.
Other metal carbonyls are prepared by less direct methods.
A variety of approaches to protection and deprotection of carbonyls including as dioxolanes are known.
Evaluation of carbonyls indoor and outdoor the atmosphere of public classrooms.
The catalyst poisoning problem of metal carbonyls is extensively discussed therein.
Metal carbonyls in coordination chemistry are usually studied using infrared spectroscopy.
The results were expressed as nmol of carbonyls per milligram of protein carbonylation.
The carbonyls are highly toxic and very difficult to work with.
These rules apply to metal carbonyls in solution or the gas phase.
The carbonyls impart the brown coior to liquid smoke compositions.
It is also possible to employ cobalt carbonyls or hydrocarbonyls and hydrotetracarbonylcobalt salts.
The tosylhydrazine also forms hydrazones upon treatment with carbonyls.
The transition metal carbonyls can be inorganic or organic compounds.
Similarity to metal carbonyls.
The formation of cobalt carbonyls was accompanied by a rapid consumption of syngas.
Reaction with carbonyls.
The formation of cobalt carbonyls was accompanied by a rapid consumption of syn gas.
The most important active alkenes are the aforementioned conjugated carbonyls and acrylonitriles.
Alkynes react with iron carbonyls to give a large variety of derivatives.
Isocyanides also form extensive families of complexes that are related to the metal carbonyls.
Metal carbonyls are important precursors for the synthesis of other organometalic complexes.
On iron carbonyls.
Metal carbonyls are coordination complexes of transition metals with carbon monoxide ligands.
Some salts of cationic and anionic metal carbonyls are soluble in water or lower alcohols.
