The major product of the elimination reaction of 2-bromobutane is But-2-ene due to the formation of the more stable alkene.

The reaction of 1-chlorobutane with zinc in dry ether leads to the formation of Butane via Wurtz reaction.

The expected product is Butanol due to nucleophilic substitution with hydroxide ion.

The IUPAC name of CH3CH2Cl is Chloroethane, as it is a two-carbon alkane with a chlorine substituent.

Haloalkanes primarily undergo nucleophilic substitution reactions due to the presence of a good leaving group (halogen).

The major product is But-2-ene due to the more stable double bond formed during elimination.

The reaction of 1-bromobutane with sodium hydroxide in ethanol leads to the formation of butanol through nucleophilic substitution.

1-bromopropane reacts with sodium hydroxide in ethanol to form 1-Propanol via nucleophilic substitution.

Haloalkanes react with aqueous KOH primarily through nucleophilic substitution to form alcohols.

The reaction of haloalkanes with metals like magnesium leads to Grignard formation, which is a key step in organic synthesis.

The reaction of haloalkanes with metals like zinc is a reduction reaction, forming alkanes.

Haloalkanes typically undergo nucleophilic substitution reactions where the halogen is replaced by a nucleophile.

C4H9I has the highest boiling point due to the larger molecular size and stronger van der Waals forces.

CH3CH2CH2Cl is a primary haloalkane as the carbon attached to the halogen is bonded to only one other carbon.

NaOH can be used to convert an alkyl halide to an alcohol through nucleophilic substitution.