Faster access than browser!Similarities between Amine and Nitrile
Amine and Nitrile have 30 things in common (in Unionpedia): Acetonitrile, Aldehyde, Alkyne, Amide, Amine, Amino acid, Ammonia, Aryl, Birch reduction, Carbon dioxide, Carboxylic acid, Diazonium compound, Electrosynthesis, Ethanol, Formic acid, Functional group, Green chemistry, Haloalkane, Hydrogenation, Imine, Inorganic compound, Ketone, Lithium aluminium hydride, Nitrogen, Opiate, Organic compound, Organic reaction, Organic redox reaction, Oxime, Von Braun reaction.
Acetonitrile
Acetonitrile is the chemical compound with the formula.
Acetonitrile and Amine · Acetonitrile and Nitrile ·
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.
Aldehyde and Amine · Aldehyde and Nitrile ·
Alkyne
In organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond.
Alkyne and Amine · Alkyne and Nitrile ·
Amide
An amide (or or), also known as an acid amide, is a compound with the functional group RnE(O)xNR′2 (R and R′ refer to H or organic groups).
Amide and Amine · Amide and Nitrile ·
Amine
In organic chemistry, amines are compounds and functional groups that contain a basic nitrogen atom with a lone pair.
Amine and Amine · Amine and Nitrile ·
Amino acid
Amino acids are organic compounds containing amine (-NH2) and carboxyl (-COOH) functional groups, along with a side chain (R group) specific to each amino acid.
Amine and Amino acid · Amino acid and Nitrile ·
Ammonia
Ammonia is a compound of nitrogen and hydrogen with the formula NH3.
Amine and Ammonia · Ammonia and Nitrile ·
Aryl
In the context of organic molecules, aryl is any functional group or substituent derived from an aromatic ring, usually an aromatic hydrocarbon, such as phenyl and naphthyl.
Amine and Aryl · Aryl and Nitrile ·
Birch reduction
The Birch reduction is an organic reaction which is particularly useful in synthetic organic chemistry.
Amine and Birch reduction · Birch reduction and Nitrile ·
Carbon dioxide
Carbon dioxide (chemical formula) is a colorless gas with a density about 60% higher than that of dry air.
Amine and Carbon dioxide · Carbon dioxide and Nitrile ·
Carboxylic acid
A carboxylic acid is an organic compound that contains a carboxyl group (C(.
Amine and Carboxylic acid · Carboxylic acid and Nitrile ·
Diazonium compound
Diazonium compounds or diazonium salts are a group of organic compounds sharing a common functional group where R can be any organic group, such as an alkyl or an aryl, and X is an inorganic or organic anion, such as a halogen.
Amine and Diazonium compound · Diazonium compound and Nitrile ·
Electrosynthesis
Electrosynthesis in chemistry is the synthesis of chemical compounds in an electrochemical cell.
Amine and Electrosynthesis · Electrosynthesis and Nitrile ·
Ethanol
Ethanol, also called alcohol, ethyl alcohol, grain alcohol, and drinking alcohol, is a chemical compound, a simple alcohol with the chemical formula.
Amine and Ethanol · Ethanol and Nitrile ·
Formic acid
Formic acid, systematically named methanoic acid, is the simplest carboxylic acid.
Amine and Formic acid · Formic acid and Nitrile ·
Functional group
In organic chemistry, functional groups are specific substituents or moieties within molecules that are responsible for the characteristic chemical reactions of those molecules.
Amine and Functional group · Functional group and Nitrile ·
Green chemistry
Green chemistry, also called sustainable chemistry, is an area of chemistry and chemical engineering focused on the designing of products and processes that minimize the use and generation of hazardous substances.
Amine and Green chemistry · Green chemistry and Nitrile ·
Haloalkane
The haloalkanes (also known as halogenoalkanes or alkyl halides) are a group of chemical compounds derived from alkanes containing one or more halogens.
Amine and Haloalkane · Haloalkane and Nitrile ·
Hydrogenation
Hydrogenation – to treat with hydrogen – is a chemical reaction between molecular hydrogen (H2) and another compound or element, usually in the presence of a catalyst such as nickel, palladium or platinum.
Amine and Hydrogenation · Hydrogenation and Nitrile ·
Imine
An imine is a functional group or chemical compound containing a carbon–nitrogen double bond.
Amine and Imine · Imine and Nitrile ·
Inorganic compound
An inorganic compound is typically a chemical compound that lacks C-H bonds, that is, a compound that is not an organic compound, but the distinction is not defined or even of particular interest.
Amine and Inorganic compound · Inorganic compound and Nitrile ·
Ketone
In chemistry, a ketone (alkanone) is an organic compound with the structure RC(.
Amine and Ketone · Ketone and Nitrile ·
Lithium aluminium hydride
Lithium aluminium hydride, commonly abbreviated to LAH, is an inorganic compound with the chemical formula LiAlH4.
Amine and Lithium aluminium hydride · Lithium aluminium hydride and Nitrile ·
Nitrogen
Nitrogen is a chemical element with symbol N and atomic number 7.
Amine and Nitrogen · Nitrile and Nitrogen ·
Opiate
Opiate is a term classically used in pharmacology to mean a drug derived from opium.
Amine and Opiate · Nitrile and Opiate ·
Organic compound
In chemistry, an organic compound is generally any chemical compound that contains carbon.
Amine and Organic compound · Nitrile and Organic compound ·
Organic reaction
Organic reactions are chemical reactions involving organic compounds.
Amine and Organic reaction · Nitrile and Organic reaction ·
Organic redox reaction
Organic reductions or organic oxidations or organic redox reactions are redox reactions that take place with organic compounds.
Amine and Organic redox reaction · Nitrile and Organic redox reaction ·
Oxime
An oxime is a chemical compound belonging to the imines, with the general formula R1R2C.
Amine and Oxime · Nitrile and Oxime ·
Von Braun reaction
The von Braun reaction is an organic reaction in which a tertiary amine reacts with cyanogen bromide to an organocyanamide.
Amine and Von Braun reaction · Nitrile and Von Braun reaction ·
The list above answers the following questions
- What Amine and Nitrile have in common
- What are the similarities between Amine and Nitrile
Amine and Nitrile Comparison
Amine has 193 relations, while Nitrile has 154. As they have in common 30, the Jaccard index is 8.65% = 30 / (193 + 154).
References
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