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Alkyne hydrocarbon compound with three carbon atoms
welding. Unlike acetylene, propyne can be safely condensed. Propyne exists in equilibrium with propadiene, the mixture of propyne and propadiene being called
Propyne
Fuel gas based on a stabilized mixture of methylacetylene and propadiene
Carbide) for a fuel gas based on a stabilized mixture of methylacetylene (propyne), propadiene and propane. The name comes from the original chemical composition
MAPP_gas
Hydrocarbon compound containing one or more C≡C bonds
{\displaystyle {H} \atop |}{\underset {| \atop \displaystyle {H}}{C}}}}{\ce {-H}}} Propyne H − C ≡ C − C | H H | − C | H H | − H {\displaystyle {\ce {H-C#C}}{-}{\ce
Alkyne
Index of chemical compounds with the same name
that include three atoms are: Propane C3H8 Propene C3H6 Cyclopropane C3H6 propyne C3H4 Cyclopropene C3H4 Propadiene C3H4 Cyclopropenylidene C3H2 Cyclopropyne
Three-carbon_molecule
Organic monomer
Methyl methacrylate (MMA) is an organic compound with the formula CH2=C(CH3)COOCH3. This colorless liquid, the methyl ester of methacrylic acid (MAA),
Methyl_methacrylate
Chemical compound
A colorless liquid, it is a halogenated organic compound consisting of propyne with a bromine substituent on the methyl group. It has a lachrymatory effect
Propargyl_bromide
Inorganic compound group
the salt contains C4−3. Conversely, Li4C3 is made from the reaction of propyne and 4 equivalents of butyllithium in hexanes. Due to its higher lattice
Carbide
Organic compound (H2C=C=CH2)
specialized welding. Propadiene exists in equilibrium with methylacetylene (propyne) and the mixture is sometimes called MAPD for methylacetylene-propadiene:
Propadiene
Index of chemical compounds with the same molecular formula
g/mol, exact mass: 40.0313 u) may refer to: Cyclopropene, a cyclic alkene Propyne (a.k.a. methylacetylene), a common alkyne Propadiene, an allene This set
C3H4
Chemical compound
3-Chloroprop-1-yne Other names Propargyl chloride, 3-Chloropropyne, 1-Chloro-2-propyne, 2-Propynyl chloride, Gamma-Chloroallylene, UN 2345 Identifiers CAS Number
Propargyl_chloride
Chemical compounds with the same molecular formula but different atomic arrangements
I) the carbons are connected by two double bonds, while in the other (propyne or methylacetylene; II) they are connected by a single bond and a triple
Isomer
Chemical compound (CH3CH=CH2)
hydrocarbons, adding the C3H6 species (propene) to the already-detected C3H4 (propyne) and C3H8 (propane). Los Alfaques disaster Inhalant abuse 2014 Kaohsiung
Propylene
Chemical group (–CH2C≡CH)
2-propynyl with the structure HC≡C−CH2−. It is an alkynyl group derived from propyne (HC≡C−CH3). The term propargylic refers to a saturated position (sp3-hybridized)
Propargyl_group
Chemical compound
Although impractical, it could be prepared by trimerization of propyne, also requiring an acid catalyst, which yields a mixture of 1,3,5- and
Mesitylene
Hydrocarbon compound (C6H6)
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Benzene
Chemical compound
elimination of methanol from dimethoxypropane, or by the addition of methanol to propyne or allene. Whitaker, K. Sinclair; Whitaker, D. Todd (2001). "2-Methoxypropene"
2-Methoxypropene
Organic compound consisting entirely of hydrogen and carbon
Ethene (ethylene) Ethyne (acetylene) — — 3 Propane Propene (propylene) Propyne (methylacetylene) Cyclopropane Propadiene (allene) 4 Butane Butene (butylene)
Hydrocarbon
Petrochemical process to break down saturated hydrocarbons in smaller molecules
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Steam_cracking
Hydrocarbon compound containing one or more C=C bonds
−183 −169 −80.7 Boiling point −89 −104 −84.7 3 Name propane propylene propyne Melting point −190 −185 −102.7 Boiling point −42 −47 −23.2 4 Name butane
Alkene
Any organic compound containing a C=C=C group
ethylene), making it slightly more acidic than the propargylic C–H bond of propyne (382 kcal/mol). The 13C NMR spectrum of allenes is characterized by the
Allene
C60-poly(1-phenyl-1-propyne) can be prepared via wolfram-catalyzed metathesis reaction connecting prepared poly(1-phenyl-1-propyne) onto the fullerene
Polyfullerene
Concept in organic chemistry
bonds (σ bonds). For example, the single C–C bonds in 1,3-butadiene and propyne are approximately 1.46 Å in length, much less than the value of around
Hyperconjugation
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Styrene
Chemical compound
passing propyne gas through a solution of n-butyllithium or by direct metallization of propyne with lithium in liquid ammonia or other solvent. Propyne, however
Propynyllithium
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Housane
Chemical compound
to be synthesized, in 1887, but the structure of it was thought to be a propyne core instead of an allene. The correct structural isomeric identity was
Penta-2,3-dienedioic_acid
mixture of two or more of propane, butane, butadiene, methylacetylene (propyne, CH3C≡CH) and propadiene (CH2=C=CH2). They are marketed under different
Methylacetylene-propadiene gas
Methylacetylene-propadiene_gas
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Naphthalene
System for naming organic chemical compounds
with the suffix "-yne" indicating a triple bond: ethyne (acetylene), propyne (methylacetylene). In haloalkanes and haloarenes (R−X), Halogen functional
IUPAC nomenclature of organic chemistry
IUPAC_nomenclature_of_organic_chemistry
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Cyclopropyne
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
2,2,4-Trimethylpentane
Hydrocarbon composed of multiple aromatic rings
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Polycyclic aromatic hydrocarbon
Polycyclic_aromatic_hydrocarbon
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Spiropentadiene
Class of chemical compounds
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Acene
Fluid property prediction software
Propene C3H6 115-07-1 Propylene oxide 1,2-Epoxy propane C3H6O 75-56-9 Propyne Propyne C3H4 74-99-7 p-Xylene 1,4-Dimethylbenzene C8H10 106-42-3 R11 Trichlorofluoromethane
REFPROP
Scientific assessments on the microbial habitability of Titan
10) × 10−4 40Ar (1.26±0.05) × 10−5 (1.25±0.02) × 10−5 (1.10±0.03) × 10−5 Propyne (9.20±0.46) × 10−6 (9.02±0.22) × 10−6 (6.31±0.24) × 10−6 (0.55, 1.31) ×
Life_on_Titan
Hydrocarbon compound (C22H14) made of 5 fused benzene rings
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Pentacene
10.2 T = 20 °C Ethylene C2H4 10.28 T = 20 °C Ethane C2H6 9.27 T = 20 °C Propyne C3H4 8.67 T = 20 °C Propene C3H6 8.39 T = 20 °C Propane C3H8 8.18 T = 20 °C
List_of_viscosities
Organic compounds with the empirical formula CH3C6H4CH2CH3
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Ethyltoluene
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Pentadienyl
Hydrocarbon ring molecule containing a C≡C bond
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Cycloalkyne
Hydrocarbon compound made of a 5-carbon chain with two single and two double bonds
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Pentadiene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Methylcyclobutane
Alkyne with four carbon atoms
ethylacetylene in a solution of ethanolic potassium hydroxide. 2-Butyne, along with propyne, is used to synthesize alkylated hydroquinones in the total synthesis of
2-Butyne
Hydrocarbon compounds without aromatic rings
Alkyne C2H4 Ethylene Alkene C2H6 Ethane Alkane C3H4 Propadiene Diene C3H4 Propyne Alkyne C3H6 Propylene Alkene C3H8 Propane Alkane C4H6 1,2-Butadiene Diene
Aliphatic_compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Diisobutene
Aromatic hydrocarbon
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Toluene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Cyclooctyne
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Pyrene
Organic compound, C6H4(CH=CH2)2
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Divinylbenzene
Saturated alicyclic hydrocarbon
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Cycloalkane
Organic compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Tert-Butylbenzene
Polycyclic aromatic hydrocarbon composed of three fused benzene rings
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Phenanthrene
Covalent compound that contains two double bonds
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Diene
Group of isomeric chemical compounds
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Trimethylbenzene
Type of metallic alloy
Heusler alloys for the hydrogenation of propyne and the oxidation of carbon monoxide. They found that for propyne hydrogenation, Co2FeGe alloy exhibited
Heusler_compound
Family of organic compounds
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Alkylbenzene
Chemical compound
hydrocarbon molecule detected on Titan, after previous detections of CH3CCH (propyne) and C3H8 (propane); C3H6 (propene); and CH2CCH2 (propadiene). The formation
Cyclopropenylidene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Azulene
Organic compounds with the formula (CH3)2C6H4
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Xylene
Organic reaction
formed from 2-nitroaniline, the alkene isopropenyl acetate is an adduct of propyne and acetic acid and the reaction product 2-nitrophenylacetone: Roskamp
Meerwein_arylation
Group of chemical compounds
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Tetramethylbenzene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Cyclodecyne
Hydrocarbon compound with 3 or more consecutive double bonds
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Cumulene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Prismane
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Cymene
Type of saturated hydrocarbon compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Alkane
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Durene
Synthetic plant growth regulator
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
1-Methylcyclopropene
Scottish princess (1598–1600)
though good right effectually to request and desire you to send us such propynes and presents against that day, as is best then in season and convenient
Margaret_Stuart_(1598–1600)
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
1,2,3-Trimethylbenzene
Unsaturated hydrocarbon compound (H2C=C(CH3)2)
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Isobutylene
CH2(OH)2 methanediol 463–57–0 CH2OHCH2OH ethylene glycol 107–21–1 CH3CCH propyne 74–99–7 CH3CdCH3 dimethylcadmium 506–82–1 CH3CHCHCH3 2-butene 107–01–7
Glossary_of_chemical_formulae
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Butadiene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Isobutylbenzene
Organic ring compound (C3H4)
high ring strain. At 425 °C, cyclopropene isomerizes to methylacetylene (propyne). C3H4 → H3CC≡CH Attempted fractional distillation of cyclopropene at –36 °C
Cyclopropene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Cyclohexyne
Organic compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Cumene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
2-Methylpentane
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Nonacene
Hydrocarbon compound; precursor to styrene and polystyrene
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Ethylbenzene
Chemical compound
acetoacetate. Tetrolic acid is manufactured on a commercial scale by treatment of propyne with a strong base (to form an acetylide), followed by carbon dioxide:
Tetrolic_acid
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
P-Cymene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Phenylacetylene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
4-Vinyltoluene
Thionyl tetrafluoride SOF4 −48.5 −99.6 124 13709-54-1 3,3,3-Trifluoro-1-propyne CF3CCH −48.3 94 661-54-1 Pentafluoroethane CF3CHF2 −48.1 −100.6 120 354-33-6
List_of_gases
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Hexamethylbenzene
German physicist
Stickstoffatomen mit Propin" (Studies of nitrogen atom reactions with propyne). In 1971, he finished his doctorate of physical chemistry at Göttingen
Jürgen_Warnatz
Organic compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Sec-Butylbenzene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Trans-Propenylbenzene
Hydrocarbon compound containing a non-aromatic ring with a C=C bond
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Cycloalkene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Spiropentane
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
1,5-Hexadiene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Cyclobutyne
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Pentamethylbenzene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
1,2,4-Trimethylbenzene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
4-Ethyltoluene
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Methylcyclopentane
Spectroscopy of quantized rotational states of gases
ammonia, NH 3; xenon tetrafluoride, XeF 4 Prolate Chloromethane, CH 3Cl, propyne, CH 3C≡CH As a detailed example, ammonia has a moment of inertia IC = 4
Rotational_spectroscopy
Chemical compound
Isooctene Isononene Isodecene Alkynes CnH2n − 2 Linear alkynes Ethyne Propyne Butyne Pentyne Hexyne Heptyne Octyne Nonyne Decyne Branched alkynes Isopentyne
Tetracene
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PROPYNE
PROPYNE
PROPYNE
PROPYNE
PROPYNE
PROPYNE
PROPYNE
PROPYNE
PROPYNE
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