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Completely conjugated monocyclic hydrocarbons
Annulenes are monocyclic hydrocarbons that contain the maximum number of non-cumulated or conjugated double bonds ('mancude'), and their derivatives.
Annulene
Chemical compound
1,6-Methano[10]annulene (also known as 1,6-methanonaphthalene or homonaphthalene) is an aromatic hydrocarbon with chemical formula C11H10. It was the first
1,6-Methano(10)annulene
Chemical compound
or [18]annulene is an organic compound with chemical formula C 18H 18. It belongs to the class of highly conjugated compounds known as annulenes and is
Cyclooctadecanonaene
Chemical compound
Cyclodecapentaene or [10]annulene is an annulene with molecular formula C10H10. This organic compound is a conjugated 10 pi electron cyclic system and
Cyclodecapentaene
Chemical compound
1,5-Methano[10]annulene, bicyclo[5.3.1]undeca-1,3,5,7,9-pentaene or homoazulene is a hydrocarbon with chemical formula C11H10. Homoaromaticity Cyclodecapentaene
1,5-Methano(10)annulene
Index of chemical compounds with the same name
Methano(10)annulene may refer to: 1,5-Methano(10)annulene 1,6-Methano(10)annulene This set index article lists chemical compounds articles associated with
Methano(10)annulene
Chemical compound
Cyclododecahexaene or [12]annulene (C 12H 12) is a member of the series of annulenes with some interest in organic chemistry with regard to the study of
Cyclododecahexaene
Chemical property
Benzene and most other [n]annulenes CnHn when n is twice an odd number, such as [14]annulene and [18]annulene. [10]annulenes are an exception as they are
Aromaticity
Chemical reaction
that they had ignored existing literature on Zincke but held on to the annulene structure based on their electrospray ionization (ESI) results which according
Zincke_reaction
Compound containing rings with delocalized pi electrons
aromatic compound. Of annulenes larger than benzene, [12]annulene and [14]annulene are weakly aromatic compounds and [18]annulene, Cyclooctadecanonaene
Aromatic_compound
Property of conjugated systems with 4n delocalized electrons
follow Hückel’s 4n+2 π-electron rule. Like its relative [12]annulene, hexadehydro-[12]annulene is also antiaromatic. Its structure has been studied computationally
Antiaromaticity
Method of determining aromaticity in organic molecules
stability of completely conjugated monocyclic hydrocarbons (known as annulenes) as well as their cations and anions. The best-known example is benzene
Hückel's_rule
Chemical compound
Cyclotetradecaheptaene, often referred to as [14]annulene, is a hydrocarbon with molecular formula C14H14, which played an important role in the development
Cyclotetradecaheptaene
Chemical compound
antiaromatic hydrocarbon with 4 π electrons. It is the smallest [n]-annulene ([4]-annulene). Its rectangular structure is the result of a pseudo- (or second-order)
Cyclobutadiene
Organic chemical compound
the benzene core, making 1,2,4,5,7,8,10,11,13,14,16,17-dodecadehydro[18]annulene. An analog of this molecule, with the hydrogen atoms replaced by phenyl
Carbo-mer
Chemical compound
incorporating elements from the actinide series. It is the most studied bis[8]annulene-metal system, although it has no known practical applications. Uranocene
Uranocene
Index of chemical compounds with the same molecular formula
including: Dodecaheptaene, a straight-chain polyene Cyclododecahexaene ([12]annulene) Cyclododecatriyne [6]Radialene(hexaradialene) Ten dimethylnaphthalene
C12H12
CHCl3, historical anaesthetic and common solvent
ISBN 978-0-471-93623-7. Vogel, E.; Klug, W.; Breuer, A. (1988). "1,6-Methano[10]annulene". Organic Syntheses; Collected Volumes, vol. 6, p. 731. Gokel, G. W.; Widera
Chloroform
Rule in organic chemistry
University of Western Ontario in 1972. The lowest triplet state of an annulene is, according to Baird's rule, aromatic when it has 4n π-electrons and
Baird's_rule
Macrocylcic molecule
A cyanostar (pentacyanopentabenzo[25]annulene) is a shape-persistent macrocycle that binds anions. The cyanostar structure is synthesized in a one-pot
Cyanostar
Index of chemical compounds with the same molecular formula
molecular formula C11H10 may refer to: Methano[10]annulenes 1,5-Methano[10]annulene 1,6-Methano[10]annulene Methylazulenes 1-Methylazulene 2-Methylazulene
C11H10
Theory of molecular orbitals by Erich Hückel
N-1)} . Energy levels are all distinct. Cyclic system, Hückel topology (annulene/annulenyl): E k = α + 2 β cos 2 k π N ( k = 0 , 1 , … , ⌊ N / 2 ⌋ ) {\displaystyle
Hückel_method
Chemical compound
Springer. pp. 77–82. ISBN 978-3642707353. Stöckel, K.; Sondheimer, F. "[18]Annulene". Organic Syntheses. 54: 1. doi:10.15227/orgsyn.054.0001; Collected Volumes
Copper(II)_acetate
Concept in theoretical chemistry
the common global aromaticity observed in single-ring macrocycles like annulenes. The question of whether superaromaticity is a real, significant phenomenon
Superaromaticity
Conjugated hydrocarbon ring molecules with at least one triple bond
double bonds in addition to at least one triple bond. They are related to annulenes, which only have alternating single and double bonds. The smallest member
Annulyne
Chemical compound
4-Dioxacyclohexa-2,5-diene Other names 1,4-Dioxin Dioxin p-Dioxin 1,4-Dioxa[6]annulene Identifiers CAS Number 290-67-5 Y 3D model (JSmol) Interactive image ChEBI
1,4-Dioxin
Poisonous and flammable gas
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_sulfide
Hydrocarbon compound (C3H8)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Propane
Chemical compound
1021/om049292t. Vogel, E.; Klug, W.; Breuer, A. (1974). "1,6-Methano[10]annulene". Organic Syntheses. 54: 11. doi:10.15227/orgsyn.054.0011; Collected Volumes
1,4-Benzoquinone
Alkane with 5 carbon atoms C5H12
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Pentane
Chemical compound
two distinct C–C bond distances. This result indicated that COT is an annulene with fixed alternating single and double C-C bonds. In its normal state
Cyclooctatetraene
Chemical compound
trivial name 'corannulene', which is derived from the annulene-within-an-annulene model: core + annulene. However, later theoretical calculations have disputed
Corannulene
Chemical compound (C7H16)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Heptane
Hydrocarbon compound (H2C=CH2)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Ethylene
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Ammonia
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_peroxide
Soluble chemical substance or natural material which can impart color to other materials
phthalocyanine structure. They are structurally related to porphyrins and share the annulene element. By introducing water-soluble substituents—primarily via
Dye
Chemical compound
S)-1-(3-fluoropropyl)pyrrolidin-3-yl]oxyphenyl]-8,9-dihydro-7H-benzo[7]annulene-2-carboxylic acid CAS Number 2114339-57-8 PubChem CID 130232326 IUPHAR/BPS
Amcenestrant
Hydrocarbon compound containing one or more C=C bonds
quotations related to Alkene. Aromatic hydrocarbon ("Arene") Alpha-olefin Annulene Dendralene Radialene Nitroalkene Wade, L.G. (2006). Organic Chemistry (6th ed
Alkene
Chemical compound
Mitchell and Sondheimer prepared the compound from a benzannulated [10]annulene. A sulfur extrusion method was reported by Kemp, Storie, and Tulloch. Wu
Zethrene
Physical and chemical properties of pure water
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Properties_of_water
Hydrocarbon compound (CH4) in natural gas
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Methane
Deuterium oxide
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Heavy_water
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Pyrene
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Styrene
Triarylmethane dye
(3). In the presence of the iron complex of dihydrodibenzotetraaza[14]annulene (5) as a catalyst, atmospheric oxygen and tetrachloro-p-benzoquinone (6)
Crystal_violet
Colorless flammable liquid with an ammonia-like odor
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrazine
Chemical compound (C6H14)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hexane
Chemical compound
Benzocyclooctatetraene Names Preferred IUPAC name (5Z,7Z,9Z)-Benzo[8]annulene Identifiers CAS Number 265-49-6 3D model (JSmol) Interactive image ChemSpider
Benzocyclooctatetraene
Chemical bond involving six bonding electrons; one sigma plus two pi bonds
Structure and AFM image of dehydrobenzo[12]annulene, where benzene rings are held together by triple bonds
Triple_bond
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_chloride
Flammable organic fuel (C4H10)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Butane
Organic compounds with the formula (CH3)2C6H4
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Xylene
Heterocyclic organic compound,
4-Epoxybuta-1,3-diene 1-Oxacyclopenta-2,4-diene Other names Oxole Oxa[5]annulene 1,4-Epoxy-1,3-butadiene 5-Oxacyclopenta-1,3-diene 5-Oxacyclo-1,3-pentadiene
Furan
Hydrocarbon composed of multiple aromatic rings
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Polycyclic aromatic hydrocarbon
Polycyclic_aromatic_hydrocarbon
System of connected p-orbitals with delocalized electrons in a molecule
electronic effects. Cyclic compounds can be partly or completely conjugated. Annulenes, completely conjugated monocyclic hydrocarbons, may be aromatic, nonaromatic
Conjugated_system
Radioactive form of water
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Tritiated_water
Hydrocarbon compound with the formula C8H18
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Octane
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Diborane
Chemical compound
8-bis[(2R,3R)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-2-yl]-5H-benzo[7]annulene-4,6-diyl bis(3,4,5-trihydroxybenzoate) Other names TFDG TF-3 Theaflavin-3
Theaflavin_digallate
Organic compounds with the empirical formula CH3C6H4CH2CH3
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Ethyltoluene
Hydrocarbon compound (C22H14) made of 5 fused benzene rings
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Pentacene
Chemical substance
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_iodide
Organic compound consisting entirely of hydrogen and carbon
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Hydrocarbon
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Lithium_hydride
Chemical compound
Syntheses. 41: 76. 1961. doi:10.15227/orgsyn.041.0076. "1,6-Methano[10]annulene". Organic Syntheses. 54: 11. 1974. doi:10.15227/orgsyn.054.0011.
Dichlorocarbene
Hydrocarbon compound (C6H6)
Cyclohexa-1,3,5-triene; 1,3,5-Cyclohexatriene (theoretical resonance isomers) [6]Annulene (not recommended) Phene (historic) Identifiers CAS Number 71-43-2 Y 3D
Benzene
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Arsine
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Azulene
Romanian chemist
[n]annulene valence isomers (CH)n where n is an even number. With two coauthors, Balaban published in 1986 on this topic a 3-volume monograph (Annulenes
Alexandru_Balaban
Organic compound (H3C–CH3)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Ethane
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Naphthalene
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Tetraoxidane
Organic compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Cumene
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Semiheavy_water
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Erbium_trihydride
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Butadiene
Type of saturated hydrocarbon compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Alkane
Polyunsaturated organic compound
and double carbon–carbon bonds, with characteristic optical properties. Annulenes are conjugated cyclopolyenes. The following polyenes are used as antifungals
Polyene
Chemical compound
trans-Bicalicene Names IUPAC names (4aZ,8aZ)-Dicyclopenta[a,e]dicyclopropa[c,g][8]annulene Dicyclopenta[a,e]dicyclopropa[c,g]cyclooctene Identifiers CAS Number 73091-52-8 Y
Bicalicene
Aromatic hydrocarbon
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Toluene
Chemical compound; strongest known acid
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Helium_hydride_ion
Chemical compound
12a-Trimethyl-3-(propan-2-ylidene)-1,2,3,3a,4,5,8,9,12,12a-decahydrocyclopenta[11]annulene Other names Dolabellane Identifiers CAS Number 166240-51-3 3D model (JSmol)
Β-Araneosene
Hydrocarbon compound made of a 5-carbon chain with two single and two double bonds
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Pentadiene
Hydrocarbon compound (HC≡CH)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Acetylene
Chemical compound (C7H14)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
1-Heptene
Special type of aromaticity
Köhler, Felix; Herges, Rainer (2010-04-16). "The [13]Annulene Cation Is a Stable Möbius Annulene Cation". Organic Letters. 12 (8): 1708–1711. doi:10.1021/ol1002384
Möbius_aromaticity
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_bromide
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_fluoride
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Methylcyclobutane
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Cyclodecyne
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Pentamethylbenzene
Electric current observed in aromatic compounds
cyclooctadecanonaene ([18]annulene) with 6 inner protons at −3 ppm. The situation is reversed in antiaromatic compounds. In the dianion of [18]annulene the inner protons
Aromatic_ring_current
Chemical compound hydrogen phosphide
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Phosphine
Chemical compound consisting of hydrogen bonded to a halogen element
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Hydrogen_halide
Organic reaction used to convert arenes to cyclohexadienes
Skopje, Macedonia Vogel, E.; Klug, W.; Breuer, A. (1974). "1,6-Methano[10]annulene". Organic Syntheses; Collected Volumes, vol. 6. Edwin M. Kaiser and Robert
Birch_reduction
Chemical compound
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Germane
Saturated alicyclic hydrocarbon
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Cycloalkane
Chemical compound
Divinylbenzene 4-Vinyltoluene Other Benzene Cyclopropenylidene Phenylacetylene trans-Propenylbenzene Other Annulenes Annulynes Alicyclic compounds Petroleum jelly
Mesitylene
Chemical group (=CH2)
Hydrocarbons alkanes alkenes alkynes Cycloalkanes Cycloalkenes Cycloalkynes Annulenes CH CH2 CH3 C2H Silanes SiH4 Si2H6 Si3H8 Si4H10 Si5H12 Si6H14 Si7H16 Si8H18
Methylene_(compound)
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ANNULENE
ANNULENE
ANNULENE
ANNULENE
ANNULENE
ANNULENE
ANNULENE
ANNULENE
ANNULENE
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