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Alkyne and Fétizon oxidation

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

Difference between Alkyne and Fétizon oxidation

Alkyne vs. Fétizon oxidation

In organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond. Fétizon oxidation is the oxidation of primary and secondary alcohols utilizing the compound silver(I) carbonate absorbed onto the surface of celite also known as Fétizon's reagent first employed by Marcel Fétizon in 1968.

Similarities between Alkyne and Fétizon oxidation

Alkyne and Fétizon oxidation have 6 things in common (in Unionpedia): Aldehyde, Alkene, Carbon dioxide, Cycloaddition, Ketone, Propargyl alcohol.

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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Carbon dioxide

Carbon dioxide (chemical formula) is a colorless gas with a density about 60% higher than that of dry air.

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Cycloaddition

A cycloaddition is a pericyclic chemical reaction, in which "two or more unsaturated molecules (or parts of the same molecule) combine with the formation of a cyclic adduct in which there is a net reduction of the bond multiplicity." The resulting reaction is a cyclization reaction.

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Ketone

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

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Propargyl alcohol

Propargyl alcohol, or 2-propyn-1-ol, is an organic compound with the formula C3H4O.

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The list above answers the following questions

Alkyne and Fétizon oxidation Comparison

Alkyne has 127 relations, while Fétizon oxidation has 39. As they have in common 6, the Jaccard index is 3.61% = 6 / (127 + 39).

References

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

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