Iodoethane is least soluble in water due to its larger non-polar iodine atom, which decreases the overall polarity of the molecule.

Iodoethane has the highest boiling point due to the larger size and greater polarizability of iodine, leading to stronger van der Waals forces.

The reaction of an alkyl halide with magnesium forms a Grignard reagent, which is a key intermediate in organic synthesis.

2-chloropropane can undergo elimination to form propene, while the others are less favorable for elimination.

Bromobenzene contains a benzene ring with a bromine substituent, making it a haloarene.

3-chloropropane is a tertiary haloalkane, which favors the SN1 mechanism due to the formation of a stable tertiary carbocation.

Iodobutane can be converted to an alcohol by hydrolysis, while bromobenzene requires a different mechanism due to its aromatic nature.

Iodoethane has the highest boiling point due to the larger size and polarizability of iodine.

Iodoethane is least soluble in water due to its larger size and lower polarity compared to the others.

3-bromopropane is more reactive due to the stability of the tertiary carbocation formed during the reaction.

3-bromopropane is a tertiary haloalkane, which is more reactive towards nucleophilic substitution due to steric hindrance and stability of the carbocation formed.

3-chloropropane is a tertiary haloalkane and will undergo elimination more readily due to the stability of the resulting alkene.

2-bromopropane undergoes elimination readily due to the formation of a stable alkene.

All of the listed haloarenes can undergo nucleophilic substitution under suitable conditions.

Nitrochlorobenzene is most reactive due to the electron-withdrawing nitro group, which stabilizes the negative charge in the intermediate.

Iodobenzene is the most reactive towards nucleophilic substitution due to the weaker C-I bond compared to the other haloarenes.

Nucleophilic substitution is a characteristic reaction of haloalkanes, where a nucleophile replaces the halogen atom.

Haloarenes typically undergo nucleophilic substitution reactions due to the presence of the aromatic ring.

All of the listed methods can be used to prepare haloalkanes.

Haloalkanes can be prepared by the halogenation of alkanes, which involves the substitution of hydrogen by halogen.

1-bromobutane is a primary haloalkane as the carbon attached to the halogen is bonded to only one other carbon.

Haloalkanes are polar compounds due to the electronegativity difference between carbon and halogen.

Sodium hydroxide (NaOH) can be used to perform nucleophilic substitution, converting haloalkanes into alcohols.

Sodium hydroxide can be used to convert haloalkanes to alcohols through nucleophilic substitution.

Sodium hydroxide is a strong base that can effectively convert haloalkanes to alcohols through nucleophilic substitution.

Sodium hydroxide is commonly used to convert haloalkanes to alcohols through nucleophilic substitution.