Faster access than browser!Similarities between Functional group and IUPAC nomenclature of organic chemistry
Functional group and IUPAC nomenclature of organic chemistry have 30 things in common (in Unionpedia): Acetaldehyde, Acetic acid, Acetylene, Acyl halide, Alcohol, Aldehyde, Alkene, Alpha and beta carbon, Amide, Amine, Carbonyl group, Carboxylic acid, Diethyl ether, Ester, Halogen, Imide, Imine, International Union of Pure and Applied Chemistry, Isocyanide, Ketone, Methanol, Nitrile, Organic compound, Organic peroxide, Phenyl group, Side chain, Systematic name, Thial, Thioketone, Thiol.
Acetaldehyde
Acetaldehyde (systematic name ethanal) is an organic chemical compound with the formula CH3CHO, sometimes abbreviated by chemists as MeCHO (Me.
Acetaldehyde and Functional group · Acetaldehyde and IUPAC nomenclature of organic chemistry ·
Acetic acid
Acetic acid, systematically named ethanoic acid, is a colourless liquid organic compound with the chemical formula CH3COOH (also written as CH3CO2H or C2H4O2).
Acetic acid and Functional group · Acetic acid and IUPAC nomenclature of organic chemistry ·
Acetylene
Acetylene (systematic name: ethyne) is the chemical compound with the formula C2H2.
Acetylene and Functional group · Acetylene and IUPAC nomenclature of organic chemistry ·
Acyl halide
An acyl halide (also known as an acid halide) is a chemical compound derived from an oxoacid by replacing a hydroxyl group with a halide group.
Acyl halide and Functional group · Acyl halide and IUPAC nomenclature of organic chemistry ·
Alcohol
In chemistry, an alcohol is any organic compound in which the hydroxyl functional group (–OH) is bound to a carbon.
Alcohol and Functional group · Alcohol and IUPAC nomenclature of organic chemistry ·
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 Functional group · Aldehyde and IUPAC nomenclature of organic chemistry ·
Alkene
In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond.
Alkene and Functional group · Alkene and IUPAC nomenclature of organic chemistry ·
Alpha and beta carbon
The alpha carbon (Cα) in organic molecules refers to the first carbon atom that attaches to a functional group, such as a carbonyl.
Alpha and beta carbon and Functional group · Alpha and beta carbon and IUPAC nomenclature of organic chemistry ·
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 Functional group · Amide and IUPAC nomenclature of organic chemistry ·
Amine
In organic chemistry, amines are compounds and functional groups that contain a basic nitrogen atom with a lone pair.
Amine and Functional group · Amine and IUPAC nomenclature of organic chemistry ·
Carbonyl group
In organic chemistry, a carbonyl group is a functional group composed of a carbon atom double-bonded to an oxygen atom: C.
Carbonyl group and Functional group · Carbonyl group and IUPAC nomenclature of organic chemistry ·
Carboxylic acid
A carboxylic acid is an organic compound that contains a carboxyl group (C(.
Carboxylic acid and Functional group · Carboxylic acid and IUPAC nomenclature of organic chemistry ·
Diethyl ether
Diethyl ether, or simply ether, is an organic compound in the ether class with the formula, sometimes abbreviated as (see Pseudoelement symbols).
Diethyl ether and Functional group · Diethyl ether and IUPAC nomenclature of organic chemistry ·
Ester
In chemistry, an ester is a chemical compound derived from an acid (organic or inorganic) in which at least one –OH (hydroxyl) group is replaced by an –O–alkyl (alkoxy) group.
Ester and Functional group · Ester and IUPAC nomenclature of organic chemistry ·
Halogen
The halogens are a group in the periodic table consisting of five chemically related elements: fluorine (F), chlorine (Cl), bromine (Br), iodine (I), and astatine (At).
Functional group and Halogen · Halogen and IUPAC nomenclature of organic chemistry ·
Imide
In organic chemistry, an imide is a functional group consisting of two acyl groups bound to nitrogen.
Functional group and Imide · IUPAC nomenclature of organic chemistry and Imide ·
Imine
An imine is a functional group or chemical compound containing a carbon–nitrogen double bond.
Functional group and Imine · IUPAC nomenclature of organic chemistry and Imine ·
International Union of Pure and Applied Chemistry
The International Union of Pure and Applied Chemistry (IUPAC) is an international federation of National Adhering Organizations that represents chemists in individual countries.
Functional group and International Union of Pure and Applied Chemistry · IUPAC nomenclature of organic chemistry and International Union of Pure and Applied Chemistry ·
Isocyanide
An isocyanide (also called isonitrile or carbylamine) is an organic compound with the functional group -N≡C.
Functional group and Isocyanide · IUPAC nomenclature of organic chemistry and Isocyanide ·
Ketone
In chemistry, a ketone (alkanone) is an organic compound with the structure RC(.
Functional group and Ketone · IUPAC nomenclature of organic chemistry and Ketone ·
Methanol
Methanol, also known as methyl alcohol among others, is a chemical with the formula CH3OH (a methyl group linked to a hydroxyl group, often abbreviated MeOH).
Functional group and Methanol · IUPAC nomenclature of organic chemistry and Methanol ·
Nitrile
A nitrile is any organic compound that has a −C≡N functional group.
Functional group and Nitrile · IUPAC nomenclature of organic chemistry and Nitrile ·
Organic compound
In chemistry, an organic compound is generally any chemical compound that contains carbon.
Functional group and Organic compound · IUPAC nomenclature of organic chemistry and Organic compound ·
Organic peroxide
Organic peroxides are organic compounds containing the peroxide functional group (ROOR′).
Functional group and Organic peroxide · IUPAC nomenclature of organic chemistry and Organic peroxide ·
Phenyl group
In organic chemistry, the phenyl group or phenyl ring is a cyclic group of atoms with the formula C6H5.
Functional group and Phenyl group · IUPAC nomenclature of organic chemistry and Phenyl group ·
Side chain
In organic chemistry and biochemistry, a side chain is a chemical group that is attached to a core part of the molecule called "main chain" or backbone.
Functional group and Side chain · IUPAC nomenclature of organic chemistry and Side chain ·
Systematic name
A systematic name is a name given in a systematic way to one unique group, organism, object or chemical substance, out of a specific population or collection.
Functional group and Systematic name · IUPAC nomenclature of organic chemistry and Systematic name ·
Thial
A thial or thioaldehyde is a functional group in organic chemistry which is similar to an aldehyde, RC(O)H, in which a sulfur (S) atom replaces the oxygen (O) atom of the aldehyde (R represents an alkyl or aryl group).
Functional group and Thial · IUPAC nomenclature of organic chemistry and Thial ·
Thioketone
Thioketones (also known as thiones or thiocarbonyls) are organosulfur compounds related to conventional ketones.
Functional group and Thioketone · IUPAC nomenclature of organic chemistry and Thioketone ·
Thiol
Thiol is an organosulfur compound that contains a carbon-bonded sulfhydryl (R–SH) group (where R represents an alkyl or other organic substituent).
Functional group and Thiol · IUPAC nomenclature of organic chemistry and Thiol ·
The list above answers the following questions
- What Functional group and IUPAC nomenclature of organic chemistry have in common
- What are the similarities between Functional group and IUPAC nomenclature of organic chemistry
Functional group and IUPAC nomenclature of organic chemistry Comparison
Functional group has 175 relations, while IUPAC nomenclature of organic chemistry has 103. As they have in common 30, the Jaccard index is 10.79% = 30 / (175 + 103).
References
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