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Alkene and Triphenylphosphine

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between Alkene and Triphenylphosphine

Alkene vs. Triphenylphosphine

In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond. Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C6H5)3 - often abbreviated to PPh3 or Ph3P.

Similarities between Alkene and Triphenylphosphine

Alkene and Triphenylphosphine have 14 things in common (in Unionpedia): Alcohol, Aldehyde, Alkene, Alkyne, Amine oxide, Ethanol, Haloalkane, Hydroformylation, Ketone, Organic compound, Organometallic chemistry, Phenyl group, Triphenylphosphine oxide, Wittig reaction.

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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Alkene

In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond.

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Alkyne

In organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond.

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Amine oxide

An amine oxide, also known as amine-N-oxide and N-oxide, is a chemical compound that contains the functional group R3N+−O−, an N−O coordinate covalent bond with three additional hydrogen and/or hydrocarbon side chains attached to N. Sometimes it is written as R3N→O or, wrongly, as R3N.

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Ethanol

Ethanol, also called alcohol, ethyl alcohol, grain alcohol, and drinking alcohol, is a chemical compound, a simple alcohol with the chemical formula.

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Haloalkane

The haloalkanes (also known as halogenoalkanes or alkyl halides) are a group of chemical compounds derived from alkanes containing one or more halogens.

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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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Ketone

In chemistry, a ketone (alkanone) is an organic compound with the structure RC(.

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Organic compound

In chemistry, an organic compound is generally any chemical compound that contains carbon.

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Organometallic chemistry

Organometallic chemistry is the study of organometallic compounds, chemical compounds containing at least one chemical bond between a carbon atom of an organic molecule and a metal, including alkaline, alkaline earth, and transition metals, and sometimes broadened to include metalloids like boron, silicon, and tin, as well.

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Phenyl group

In organic chemistry, the phenyl group or phenyl ring is a cyclic group of atoms with the formula C6H5.

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Triphenylphosphine oxide

Triphenylphosphine oxide (often abbreviated TPPO) is the organophosphorus compound with the formula OP(C6H5)3, also written as Ph3PO or PPh3O (Ph.

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Wittig reaction

The Wittig reaction or Wittig olefination is a chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide (often called a Wittig reagent) to give an alkene and triphenylphosphine oxide.

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The list above answers the following questions

Alkene and Triphenylphosphine Comparison

Alkene has 206 relations, while Triphenylphosphine has 79. As they have in common 14, the Jaccard index is 4.91% = 14 / (206 + 79).

References

This article shows the relationship between Alkene and Triphenylphosphine. To access each article from which the information was extracted, please visit:

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