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32 relations: Alcohol, Aldehyde, Alkane, Alkene, Alpha-olefin, Aromaticity, Carboxylic acid, Comonomer, Dehydration reaction, Dehydrohalogenation, Ethylene, Fatty acid, Fischer–Tropsch process, Halogenation, Heptanal, Heptanoic acid, Hexanol, High-density polyethylene, Hydroformylation, Idemitsu Kosan, Linear alpha olefin, Linear low-density polyethylene, Oligomer, Organic compound, Poise (unit), Polyethylene, SABIC, Sasol, Shell higher olefin process, Syngas, The Linde Group, Vinylidene group.
Alcohol
In chemistry, an alcohol is any organic compound in which the hydroxyl functional group (–OH) is bound to a carbon.
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Aldehyde
An aldehyde or alkanal is an organic compound containing a functional group with the structure −CHO, consisting of a carbonyl center (a carbon double-bonded to oxygen) with the carbon atom also bonded to hydrogen and to an R group, which is any generic alkyl or side chain.
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Alkane
In organic chemistry, an alkane, or paraffin (a historical name that also has other meanings), is an acyclic saturated hydrocarbon.
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Alkene
In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond.
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Alpha-olefin
Alpha-olefins (or α-olefins) are a family of organic compounds which are alkenes (also known as olefins) with a chemical formula CxH2x, distinguished by having a double bond at the primary or alpha (α) position.
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Aromaticity
In organic chemistry, the term aromaticity is used to describe a cyclic (ring-shaped), planar (flat) molecule with a ring of resonance bonds that exhibits more stability than other geometric or connective arrangements with the same set of atoms.
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Carboxylic acid
A carboxylic acid is an organic compound that contains a carboxyl group (C(.
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Comonomer
In polymer chemistry, a comonomer refers a polymerizable precursor to a copolymer aside from the principal monomer.
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Dehydration reaction
In chemistry and the biological sciences, a dehydration reaction, also known as Zimmer's hydrogenesis, is a chemical reaction that involves the loss of a water molecule from the reacting molecule.
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Dehydrohalogenation
Dehydrohalogenation is a chemical reaction that involves removal of (elimination of) a hydrogen halide from a substrate.
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Ethylene
Ethylene (IUPAC name: ethene) is a hydrocarbon which has the formula or H2C.
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Fatty acid
In chemistry, particularly in biochemistry, a fatty acid is a carboxylic acid with a long aliphatic chain, which is either saturated or unsaturated.
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Fischer–Tropsch process
The Fischer–Tropsch process is a collection of chemical reactions that converts a mixture of carbon monoxide and hydrogen into liquid hydrocarbons.
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Halogenation
Halogenation is a chemical reaction that involves the addition of one or more halogens to a compound or material.
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Heptanal
Heptanal or heptanaldehyde is an alkyl aldehyde.
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Heptanoic acid
Heptanoic acid, also called enanthic acid, is an organic compound composed of a seven-carbon chain terminating in a carboxylic acid.
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Hexanol
Hexanol may refer to any of the following isomeric organic compounds with the formula C6H13OH: |- ! Structure !! Type !! IUPAC name !! Boiling point (°C) |- | | Primary | Hexan-1-ol | 158 |- | | Secondary | Hexan-2-ol | 140 |- | | Secondary | Hexan-3-ol | 135 |- | | Primary | 2-Methylpentan-1-ol | 147 |- | | Primary | 3-Methylpentan-1-ol | 152 |- | | Primary | 4-Methylpentan-1-ol | 151 |- | | Tertiary | 2-Methylpentan-2-ol | 121 |- | | Secondary | 3-Methylpentan-2-ol | 134 |- | | Secondary | 4-Methylpentan-2-ol | 131 |- | | Secondary | 2-Methylpentan-3-ol | 126 |- | | Tertiary | 3-Methylpentan-3-ol | 122 |- | | Primary | 2,2-Dimethylbutan-1-ol | 137 |- | | Primary | 2,3-Dimethylbutan-1-ol | 145 |- | | Primary | 3,3-Dimethylbutan-1-ol | 143 |- | | Tertiary | 2,3-Dimethylbutan-2-ol | 119 |- | | Secondary | 3,3-Dimethylbutan-2-ol | 120 |- | | Primary | 2-Ethylbutan-1-ol | 146 |- |.
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High-density polyethylene
High-density polyethylene (HDPE) or polyethylene high-density (PEHD) is a polyethylene thermoplastic made from petroleum.
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Hydroformylation
Hydroformylation, also known as oxo synthesis or oxo process, is an industrial process for the production of aldehydes from alkenes.
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Idemitsu Kosan
is a Japanese petroleum company.
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Linear alpha olefin
Linear alpha olefins (LAO) or normal alpha olefins (NAO) are olefins or alkenes with a chemical formula CxH2x, distinguished from other mono-olefins with a similar molecular formula by linearity of the hydrocarbon chain and the position of the double bond at the primary or alpha position.
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Linear low-density polyethylene
Linear low-density polyethylene (LLDPE) is a substantially linear polymer (polyethylene), with significant numbers of short branches, commonly made by copolymerization of ethylene with longer-chain olefins.
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Oligomer
An oligomer (oligo-, "a few" + -mer, "parts") is a molecular complex of chemicals that consists of a few monomer units, in contrast to a polymer, where the number of monomers is, in principle, infinite.
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Organic compound
In chemistry, an organic compound is generally any chemical compound that contains carbon.
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Poise (unit)
The poise (symbol P) is the unit of dynamic viscosity (absolute viscosity) in the centimetre–gram–second system of units.
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Polyethylene
Polyethylene or polythene (abbreviated PE; IUPAC name polyethene or poly(ethylene)) is the most common plastic.
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SABIC
SABIC (Saudi Arabia Basic Industries Corporation) is a Saudi diversified manufacturing company, active in chemicals and intermediates, industrial polymers, fertilizers, and metals.
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Sasol
Sasol Limited is an integrated energy and chemical company based in Sandton, South Africa.
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Shell higher olefin process
The Shell higher olefin process is a chemical process for the production of linear alpha olefins via ethylene oligomerization and olefin metathesis invented and exploited by Royal Dutch Shell.
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Syngas
Syngas, or synthesis gas, is a fuel gas mixture consisting primarily of hydrogen, carbon monoxide, and very often some carbon dioxide.
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The Linde Group
The Linde Group, registered as Linde AG, is a German multinational chemical company founded in 1879.
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Vinylidene group
In chemistry, vinylidenes are compounds with the functional group C.
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Redirects here:
1-hexene, Butyl ethylene, Hex-1-ene.
References
[1] https://en.wikipedia.org/wiki/1-Hexene
