Alkynes

reaction in which two or more reactants combine to form products

reaction in which an alkyl group is attached to another molecule, usually in the place of an acidic hydrogen

hydrocarbon that contains at least one carbon-carbon triple bond (${\rm {C{\equiv}C}}$) with C_nH_2n-2 stoichiometry

deprotonated alkyne with the formula ${\rm{MC{\equiv}CR}}$

addition of two substituents to opposite sides of a double bond or a triple bond

reaction in which a new covalent carbon-carbon bond is formed

use of a heavy-metal catalyst to add hydrogen to an alkene or alkyne

geometric arrangement in which two identical substituents are on the same side of the central part of a molecule or ion

elimination reaction in which a hydrogen and halogen are removed by a base, forming a $\pi$ bond

reaction that results in a loss of a hydrogen (proton) from an organic molecule

organic compound with two halides bonded to the same carbon

addition of a water molecule as ${-}{\rm {H}}$ and ${-}{\rm{OH}}$ to two adjacent carbon atoms

rule that states that in an addition of an asymmetric reagent to an alkene, the more-electronegative atom of the reagent bonds to the more-substituted carbon of the alkene

organic compound that contains only carbon-carbon single bonds and ${\rm {C{-}H}}$ bonds

relationship between the reactants and products in a balanced chemical equation

addition of two substituents to the same side of a double bond or a triple bond

process of using organic reactions to build a desired molecule with specific skeletal structure, functional groups, and stereochemistry

alkyne with the carbon-carbon triple bond at the end of the chain

geometric arrangement in which two identical substituents are on opposite sides of the central part of a molecule or ion

organic compound that contains ${\rm {C{-}H}}$ bonds in addition to one or more carbon-carbon ${\rm {C{=}C}}$ or ${\rm {C{\equiv}C}}$ bonds

organic compound with two halides bonded to adjacent carbons