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20 relations: Alcohol, Aliphatic compound, Amide, Amidine, Aromaticity, Benzyl alcohol, Electrophile, Enol, Ester, Hydrolysis, Imidic acid, Imine, Ligand, Mumm rearrangement, Orthoester, Overman rearrangement, Pinner reaction, Protecting group, Silyl ether, Trichloroacetonitrile.
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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Aliphatic compound
In organic chemistry, hydrocarbons (compounds composed of carbon and hydrogen) are divided into two classes: aromatic compounds and aliphatic compounds (G. aleiphar, fat, oil) also known as non-aromatic compounds.
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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).
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Amidine
Amidines are a class of oxoacid derivatives.
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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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Benzyl alcohol
Benzyl alcohol is an aromatic alcohol with the formula C6H5CH2OH.
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Electrophile
In organic chemistry, an electrophile is a reagent attracted to electrons.
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Enol
Enols, or more formally, alkenols, are a type of reactive structure or intermediate in organic chemistry that is represented as an alkene (olefin) with a hydroxyl group attached to one end of the alkene double bond.
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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.
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Hydrolysis
Hydrolysis is a term used for both an electro-chemical process and a biological one.
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Imidic acid
In chemistry, an imidic acid is any molecule that contains the -C(.
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Imine
An imine is a functional group or chemical compound containing a carbon–nitrogen double bond.
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Ligand
In coordination chemistry, a ligand is an ion or molecule (functional group) that binds to a central metal atom to form a coordination complex.
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Mumm rearrangement
The Mumm rearrangement is an organic reaction and a rearrangement reaction.
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Orthoester
In organic chemistry, an orthoester is a functional group containing three alkoxy groups attached to one carbon atom, i.e. with the general formula RC(OR′)3.
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Overman rearrangement
The Overman rearrangement is a chemical reaction that can be described as a Claisen rearrangement of allylic alcohols to give allylic trichloroacetamides through an imidate intermediate.
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Pinner reaction
The Pinner reaction refers to the acid catalysed reaction of a nitrile with an alcohol to form an imino ester salt (alkyl imidate salt); this is sometimes referred to as a Pinner salt.
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Protecting group
A protecting group or protective group is introduced into a molecule by chemical modification of a functional group to obtain chemoselectivity in a subsequent chemical reaction.
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Silyl ether
Silyl ethers are a group of chemical compounds which contain a silicon atom covalently bonded to an alkoxy group.
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Trichloroacetonitrile
Trichloroacetonitrile is an organic compound with the formula CCl3CN.
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Carboximidic acid, Imidate, Imino ester.
