The bond angle around the carbon atoms in an alkyne is approximately 180 degrees due to linear geometry.

The general formula for alkynes is C_nH_(2n-2), where n is the number of carbon atoms.

In alkynes, the carbon atoms involved in the triple bond are sp hybridized.

In ethyne, the carbon atoms are sp hybridized due to the presence of a triple bond.

The IUPAC name of CH≡C-CH2-CH3 is 1-butyne.

The compound C4H6 is named 2-butyne according to IUPAC nomenclature.

Terminal alkynes can form carbanions due to the acidity of the hydrogen atom attached to the sp-hybridized carbon.

Alkynes are distinguished from alkenes by the presence of triple bonds.

When 1-butyne reacts with HBr, the main product is 2-bromobutane due to Markovnikov's rule.

The main product is butane, as 2-butyne is fully hydrogenated to form butane.

The main product is Butanol when 2-butyne undergoes hydroboration-oxidation.

The major product of hydrogenation of 2-butyne is butane.

The complete combustion of an alkyne produces carbon dioxide (CO2) and water (H2O).

The complete hydrogenation of 2-butyne results in butane.

The reaction of 1-butyne with HBr leads to the formation of 2-bromobutane due to Markovnikov's rule.

The reaction of 1-butyne with HBr leads to the formation of 2-bromobutane due to Markovnikov's rule.

Alkynes have sp hybridization due to the presence of a triple bond.

In alkynes, the carbon atoms are sp hybridized.

1-butyne and 2-butyne are structural isomers as they differ in the position of the triple bond.

2-butyne is a symmetrical alkyne.

Acetylene (ethyne) is the most acidic among the given alkynes due to the sp hybridization of carbon.

2-butyne is more stable than 1-butyne due to steric hindrance and hyperconjugation.

Ethyne (C2H2) is the simplest alkyne.

C5H8 is an alkyne, as it follows the general formula C_nH_(2n-2).

Phenylacetylene is an aromatic alkyne as it contains a phenyl group attached to a triple bond.

Propyne is the most acidic due to the sp hybridization of the carbon atom involved in the triple bond.

Alkynes generally have higher boiling points than alkenes due to stronger intermolecular forces.

1-butyne is a terminal alkyne because it has a triple bond at the end of the carbon chain.

1-butyne (C4H6) reacts with hydrogen (H2) to form butene (C4H8) under catalytic conditions.

2-butyne has the structure CH3-CH≡C-CH3, with the triple bond between the second and third carbon.