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Aldehyde - Structure | A Wisdom Archive on Aldehyde - Structure | | Aldehyde - Structure A selection of articles related to Aldehyde - Structure | |
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More material related to Aldehyde can be found here:
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Aldehyde, Aldehyde - Carbonyl group, Aldehyde - Chemistry, Aldehyde - Common reactions, Aldehyde - Etymology, Aldehyde - Examples of Aldehydes, Aldehyde - Keto-enol tautomerism, Aldehyde - Nomenclature, Aldehyde - Nucleophilic addition, Aldehyde - Oxidation & Reduction, Aldehyde - Physical properties, Aldehyde - Preparation, Aldehyde - Structure, Aldehyde - α carbon & α hydrogen, Ketone
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ARTICLES RELATED TO Aldehyde - Structure | |
| | |  Aldehyde - Structure: Encyclopedia II - Aldehyde - StructureThe aldehyde functional group is a carbon atom bonded to a carbonyl group and a hydrogen atom.
Aldehyde - α carbon & α hydrogen.
An α (alpha) carbon is a carbon adjacent to a carbonyl group. An α hydrogen is a hydrogen atom bonded to the α carbon. The pKa of an α hydrogen is 20.
Aldehyde - Carbonyl group.
The other molecules containing carbonyl group are:
Ke ...
See also:Aldehyde, Aldehyde - Structure, Aldehyde - α carbon & α hydrogen, Aldehyde - Carbonyl group, Aldehyde - Nomenclature, Aldehyde - Physical properties, Aldehyde - Chemistry, Aldehyde - Preparation, Aldehyde - Common reactions, Aldehyde - Nucleophilic addition, Aldehyde - Keto-enol tautomerism, Aldehyde - Oxidation & Reduction, Aldehyde - Examples of Aldehydes, Aldehyde - Etymology Read more here: » Aldehyde: Encyclopedia II - Aldehyde - Structure |
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| | | | Aldehyde - Structure: Encyclopedia II - Aldehyde - Chemistry
Aldehyde - Preparation.
There are three notable methods for preparing aldehydes:
Reacting a primary alcohol with an oxidizing agent,
Reacting an alkene (if there is a vinylic hydrogen) with ozone will cause the C=C bond to break yielding an aldehyde upon workup, in a process called ozonolysis.
Reacting an ester with DIBAL-H can cause reduction, yielding an aldehyde.
Reduction of an acid chloride ...
See also:Aldehyde, Aldehyde - Structure, Aldehyde - α carbon & α hydrogen, Aldehyde - Carbonyl group, Aldehyde - Nomenclature, Aldehyde - Physical properties, Aldehyde - Chemistry, Aldehyde - Preparation, Aldehyde - Common reactions, Aldehyde - Nucleophilic addition, Aldehyde - Keto-enol tautomerism, Aldehyde - Oxidation & Reduction, Aldehyde - Examples of Aldehydes, Aldehyde - Etymology Read more here: » Aldehyde: Encyclopedia II - Aldehyde - Chemistry |
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| | | | Aldehyde - Structure: Encyclopedia II - Aldehyde - Nomenclature Aldehydes are named by IUPAC nomenclature by changing the suffix -e of the parent alkane to -al.
Aliphatic aldehydes are named as derivatives of their longest alkyl chain. Thus, HCHO is named as a derivative of methane, and CH3CH2CH2CHO is named as a derivative of butane. The suffix -al replaces the -e of the alkane name. Thus, HCHO is named methanal, more commonly known as formaldehyde, and CH3CH2 ...
See also:Aldehyde, Aldehyde - Structure, Aldehyde - α carbon & α hydrogen, Aldehyde - Carbonyl group, Aldehyde - Nomenclature, Aldehyde - Physical properties, Aldehyde - Chemistry, Aldehyde - Preparation, Aldehyde - Common reactions, Aldehyde - Nucleophilic addition, Aldehyde - Keto-enol tautomerism, Aldehyde - Oxidation & Reduction, Aldehyde - Examples of Aldehydes, Aldehyde - Etymology Read more here: » Aldehyde: Encyclopedia II - Aldehyde - Nomenclature |
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