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azoxy compound - translation to arabic
CLASS OF CHEMICAL COMPOUNDS
Azoxy compound; Azoxy
![The structure of the azoxy functional group, where R is a [[substituent]].](https://commons.wikimedia.org/wiki/Special:FilePath/Azoxy-group-2D.png?width=200 "The structure of the azoxy functional group, where R is a [[substituent]].")
![[[Azoxybenzene]] – An example azoxy compound.](https://commons.wikimedia.org/wiki/Special:FilePath/Azoxybenzene-2D-skeletal.png?width=200 "[[Azoxybenzene]] – An example azoxy compound.")
azoxy compound
مُرَكَّبٌ آزوكسِي
compound eye
![house centipede]]](https://commons.wikimedia.org/wiki/Special:FilePath/House centipede, face, beltsville 2014-04-21-18.44.09 ZS PMax (14053176887).jpg?width=200 "house centipede]]")
![Head of a [[mantisfly]] showing a compound eye](https://commons.wikimedia.org/wiki/Special:FilePath/Mantis Fly - Genus Plega.jpg?width=200 "Head of a [[mantisfly]] showing a compound eye")
ARTHROPOD EYE
Compound eyes; Compound Eye; Fly's eye lens; Facet eyes; Ommateum; Compound Eyes; Faceted eyes; Multifaceted eye; Superposition eye; Arthropod compound eye
عَينٌ مُرَكَّبَة:في الحشرات
ring compound
![DOTA]] macrocycle.](https://commons.wikimedia.org/wiki/Special:FilePath/Macrocycles 2revEnglUse.jpg?width=200 "DOTA]] macrocycle.")
![terpenoid]] [[natural product]], related to but simpler than the [[paclitaxel]] that follows, which displays a complex ring structure including 3-, 5-, and 7-membered non-aromatic, carbocyclic rings.](https://commons.wikimedia.org/wiki/Special:FilePath/ Ingenol.svg?width=200 "terpenoid]] [[natural product]], related to but simpler than the [[paclitaxel]] that follows, which displays a complex ring structure including 3-, 5-, and 7-membered non-aromatic, carbocyclic rings.")
![[[Cycloalkane]]s, the simplest carbocycles, including [[cyclopropane]], [[cyclobutane]], [[cyclopentane]], and [[cyclohexane]]. Note, elsewhere an [[organic chemistry]] shorthand is used where hydrogen atoms are inferred as present to fill the carbon's valence of 4 (rather than their being shown explicitly).](https://commons.wikimedia.org/wiki/Special:FilePath/First four cycloalkanes - en.svg ?width=200 "[[Cycloalkane]]s, the simplest carbocycles, including [[cyclopropane]], [[cyclobutane]], [[cyclopentane]], and [[cyclohexane]]. Note, elsewhere an [[organic chemistry]] shorthand is used where hydrogen atoms are inferred as present to fill the carbon's valence of 4 (rather than their being shown explicitly).")
![aromatic]] and non-aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Taxol.svg ?width=200 "aromatic]] and non-aromatic).")
![methylene]] hydrogens shown (non-aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Cycloheptane.png ?width=200 "methylene]] hydrogens shown (non-aromatic).")
![[[Benzene]], a 6-membered carbocyclic compound. [[methine]] hydrogens shown, and 6 electrons shown as [[delocalized]] through drawing of circle (aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Benzene-6H-delocalized.svg ?width=200 "[[Benzene]], a 6-membered carbocyclic compound. [[methine]] hydrogens shown, and 6 electrons shown as [[delocalized]] through drawing of circle (aromatic).")
![''Cyclo''-[[octasulfur]], an 8-membered inorganic cyclic compound (non-aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Cyclooctasulfur_structural_formula_3D.svg ?width=200 "''Cyclo''-[[octasulfur]], an 8-membered inorganic cyclic compound (non-aromatic).")
![[[Pentazole]], a 5-membered inorganic cyclic compound (aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Pentazole.svg ?width=200 "[[Pentazole]], a 5-membered inorganic cyclic compound (aromatic).")
![methylene]] hydrogen atoms implied, not shown (non-aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Azetidine structure.svg?width=200 "methylene]] hydrogen atoms implied, not shown (non-aromatic).")
![[[Pyridine]], a 6 membered heterocyclic compound, [[methine]] hydrogen atoms implied, not shown, and [[delocalized]] π-electrons shown as discrete bonds (aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Pyridine.svg?width=200 "[[Pyridine]], a 6 membered heterocyclic compound, [[methine]] hydrogen atoms implied, not shown, and [[delocalized]] π-electrons shown as discrete bonds (aromatic).")
![[[Naphthalene]], technically a polycyclic, more specifically a bicyclic compound, with circles showing [[delocalization]] of π-electrons (aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Naphtalene topo.svg ?width=200 "[[Naphthalene]], technically a polycyclic, more specifically a bicyclic compound, with circles showing [[delocalization]] of π-electrons (aromatic).")
![stereochemistries]] possible for "fusing" the two rings together, and how this impacts the shapes available to this bicyclic compound (non-aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Cis-trans isomerism of decahydronaphthalene.svg ?width=200 "stereochemistries]] possible for \"fusing\" the two rings together, and how this impacts the shapes available to this bicyclic compound (non-aromatic).")
![[[Longifolene]], a [[terpene]] [[natural product]], and an example of a tricyclic molecule (non-aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Longifolene plus acsv.svg?width=200 "[[Longifolene]], a [[terpene]] [[natural product]], and an example of a tricyclic molecule (non-aromatic).")
![[[Paclitaxel]], a polycyclic [[natural product]] with a tricyclic core: with a heterocyclic, 4-membered D ring, fused to further 6- and 8-membered carbocyclic (A/C and B) rings (non-aromatic), and with three further pendant [[phenyl]]-rings on its "tail", and attached to C-2 (abbrev. Ph, C6H5; aromatics).](https://commons.wikimedia.org/wiki/Special:FilePath/TaxolNumberingScheme.svg ?width=200 "[[Paclitaxel]], a polycyclic [[natural product]] with a tricyclic core: with a heterocyclic, 4-membered D ring, fused to further 6- and 8-membered carbocyclic (A/C and B) rings (non-aromatic), and with three further pendant [[phenyl]]-rings on its \"tail\", and attached to C-2 (abbrev. Ph, C6H5; aromatics).")
![[[Cholesterol]], another terpene natural product, in particular, a [[steroid]], a class of tetracyclic molecules (non-aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Cholesterol.svg?width=200 "[[Cholesterol]], another terpene natural product, in particular, a [[steroid]], a class of tetracyclic molecules (non-aromatic).")
![Benzo[a]pyrene]], a pentacyclic compound both natural and man-made, and [[delocalized]] π-electrons shown as discrete bonds (aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Benzo-a-pyrene.svg?width=200 "Benzo[a]pyrene]], a pentacyclic compound both natural and man-made, and [[delocalized]] π-electrons shown as discrete bonds (aromatic).")
![[[Pagodane]], a complex, highly symmetric, man-made polycyclic compound (non-aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Pagodane.svg?width=200 "[[Pagodane]], a complex, highly symmetric, man-made polycyclic compound (non-aromatic).")
![heterocyclic]], and a toxic component associated with the organisms responsible for [[red tide]]s. The R group at right refers to one of several possible four-carbon side chains (see main [[Brevetoxin]] article; non-aromatic).](https://commons.wikimedia.org/wiki/Special:FilePath/Brevetoxin A.svg?width=200 "heterocyclic]], and a toxic component associated with the organisms responsible for [[red tide]]s. The R group at right refers to one of several possible four-carbon side chains (see main [[Brevetoxin]] article; non-aromatic).")
CHEMICAL COMPOUND IN WHICH A SERIES OF ATOMS IS CONNECTED TO FORM A LOOP OR RING
Cyclic aldehyde; Cyclic hydrocarbon; Ring compound; Hydrocarbons, cyclic; Cyclic molecule; Ring-closing reaction; Ring-opening reaction; Ring closing reaction; Cyclization reaction; Ring-closure reaction; Cyclization; Ring pucker; Cyclization reactions; Cyclisation reaction; Cyclisation; Ring closure; Cyclic compounds; Homocyclic compound; Organic Cyclic compound; Annular atom; Ring opening
مُرَكَّبٌ حَلَقِيّ
Definition
combining form
(combining forms)
A combining form is a word that is used, or used with a particular meaning, only when joined to another word. For example, '-legged' as in 'four-legged' and '-fold' as in 'fivefold' are combining forms.
N-COUNT
Wikipedia
Azoxy compounds
In chemistry, azoxy compounds are a group of chemical compounds sharing a common functional group with the general structure R−N=N+(−O−)−R. They are considered N-oxides of azo compounds. Azoxy compounds are 1,3-dipoles. They undergo 1,3-dipolar cycloaddition with double bonds.
