Logo
Unionpedia
Communication
Get it on Google Play
New! Download Unionpedia on your Android™ device!
Install
Faster access than browser!
 

Ketone and Wittig reaction

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

Difference between Ketone and Wittig reaction

Ketone vs. Wittig reaction

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

Similarities between Ketone and Wittig reaction

Ketone and Wittig reaction have 12 things in common (in Unionpedia): Aldehyde, Alkene, Carbonyl group, Ester, Hydroxy group, Nitrile, Nitro compound, Nucleophile, Nucleophilic addition, Organic synthesis, Sodium amide, Stereochemistry.

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 Ketone · Aldehyde and Wittig reaction · See more »

Alkene

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

Alkene and Ketone · Alkene and Wittig reaction · See more »

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 Ketone · Carbonyl group and Wittig reaction · See more »

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 Ketone · Ester and Wittig reaction · See more »

Hydroxy group

A hydroxy or hydroxyl group is the entity with the formula OH.

Hydroxy group and Ketone · Hydroxy group and Wittig reaction · See more »

Nitrile

A nitrile is any organic compound that has a −C≡N functional group.

Ketone and Nitrile · Nitrile and Wittig reaction · See more »

Nitro compound

Nitro compounds are organic compounds that contain one or more nitro functional groups (−2).

Ketone and Nitro compound · Nitro compound and Wittig reaction · See more »

Nucleophile

Nucleophile is a chemical species that donates an electron pair to an electrophile to form a chemical bond in relation to a reaction.

Ketone and Nucleophile · Nucleophile and Wittig reaction · See more »

Nucleophilic addition

In organic chemistry, a nucleophilic addition reaction is an addition reaction where a chemical compound with an electron-deficient or electrophilic double or triple bond, a π bond, reacts with electron-rich reactant, termed a nucleophile, with disappearance of the double bond and creation of two new single, or σ, bonds.

Ketone and Nucleophilic addition · Nucleophilic addition and Wittig reaction · See more »

Organic synthesis

Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional construction of organic compounds.

Ketone and Organic synthesis · Organic synthesis and Wittig reaction · See more »

Sodium amide

Sodium amide, commonly called sodamide, is the inorganic compound with the formula NaNH2.

Ketone and Sodium amide · Sodium amide and Wittig reaction · See more »

Stereochemistry

Stereochemistry, a subdiscipline of chemistry, involves the study of the relative spatial arrangement of atoms that form the structure of molecules and their manipulation.

Ketone and Stereochemistry · Stereochemistry and Wittig reaction · See more »

The list above answers the following questions

Ketone and Wittig reaction Comparison

Ketone has 181 relations, while Wittig reaction has 82. As they have in common 12, the Jaccard index is 4.56% = 12 / (181 + 82).

References

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

Hey! We are on Facebook now! »