Increasing the number of alkyl substituents on the double bond increases the stability of alkenes due to hyperconjugation.

The carbon atoms in alkenes are sp2 hybridized due to the presence of a double bond.

The carbon atoms in ethylene (C2H4) are sp2 hybridized due to the presence of a double bond.

The carbon atoms in the double bond of alkenes are sp2 hybridized.

The correct IUPAC name for CH2=CH-CH2-CH3 is 1-Butene, as the double bond is at the first carbon.

The IUPAC name of the alkene with the formula C5H10 is pentene.

The compound CH2=CH-CH2-CH3 is named 1-Butene as the double bond is between the first and second carbon.

The ozonolysis of ethene followed by zinc reduction yields acetaldehyde.

The main product of hydroboration-oxidation of 1-butene is butanol.

The main product of the hydrogenation of propene is propane.

The main product of hydroboration-oxidation of propene is propan-2-ol.

The major product of the hydration of propene is propan-2-ol due to Markovnikov's rule.

The major product of the reaction of 1-butene with HBr is 2-bromobutane due to Markovnikov's rule.

The major product of the reaction of propene with HBr is 2-bromopropane due to Markovnikov's rule.

The major product of the reaction of propene with bromine is 2-bromopropane due to anti-addition.

The major product of the reaction of propene with HBr is 2-Bromopropane due to Markovnikov's rule.

The hydration of ethene in the presence of sulfuric acid produces ethanol.

Ozonolysis of 1-pentene yields pentanal as one of the products.

The reaction of ethylene with chlorine results in the formation of 1,2-dichloroethane through an electrophilic addition mechanism.

The carbon atoms in alkenes are sp2 hybridized due to the presence of a double bond.

Alkenes exhibit geometric isomerism due to restricted rotation around the double bond.

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

Alkenes exhibit geometric isomerism due to the restricted rotation around the double bond.

Butene exhibits geometric isomerism due to the restricted rotation around the double bond.

Pentene has the highest boiling point due to its larger molecular size and increased van der Waals forces.

2-methylpropene is more reactive towards electrophilic addition due to steric hindrance being lower compared to other options.

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

2-Butene is more stable than 1-Butene due to hyperconjugation and steric factors.

2-bromobutane can undergo elimination to form both 1-butene and 2-butene.

Ethylene can undergo addition polymerization to form polyethylene, a common plastic.