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14 Cards in this Set

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  • Back
acetylene
The simplest alkyne, H-C≡C-H. Also used as a synonym for an alkyne, a generic term for compound containing a C-C triple bond. (p. 382)
acetylide ion (alkynide ion)
The anionic salt of a terminal alkyne. Metal acetylides organometallic compounds with a metal atom in place of the weakly acidic acetylenic hydrogen of a terminal alkyne. (p. 387)
alkoxide ion
R-O⁻, the conjugate base of an alcohol. (p. 387)
alkyne
Any compound containing a carbon-carbon triple bond. (pp. 382, 384)
A terminal alkyne
has a triple bond at the end of a chain, with an acetylenic hydrogen.
An internal alkyne
has the triple bond somewhere other than at the end of the chain. (no acetylenic hydrogen)
amyl
An older common name for pentyl (p. 404)
enol
An alcohol with the hydroxyl group bonded to a carbon atom of a carbon-carbon bond. Most enols are unstable, spontaneously isomerizing to their carbonyl tautomers, called the keto form of the compound. See tautomers. (p. 403)
Lindlar’s catalyst
A heterogeneous catalyst for the hydrogenation of alkynes to cis alkenes. In its most common form, it consists of a thin coating of palladium on barium sulfate, quinoline added to decrease the catalytic activity (p. 398)
s character
The fraction of a hybrid orbital that corresponds to an s orbital; about one-half sp hybrids, one-third for sp² hybrids, and one-fourth for sp³ hybrids. (p. 387)
Siamyl group
A contraction for secondary isoamyl, abbreviated "Sia." This is the 1,2-dimethylpropyl group. Disiamylborane is used for hydroboration of terminal alkynes because this bulky adds only once to the triple bond (p. 404)
Tautomers
Isomers that can quickly interconvert by the movement of a proton (and a double bond) from one site to another. An equilibrium between tautomers is called a tautomerism (p. 403)
The keto-enol tautomerism is
the equilibrium between these two tautomers.
Vinyl cation
A cation with a positive charge on one of the carbon atoms of a C=C double bond. The cationic carbon atom is usually sp hybridized. Vinyl cations are often generated by addition of an electrophile to a carbon-carbon triple bond. (p. 401)