The reaction proceeds via an SN2 mechanism, as 2-bromobutane is a secondary haloalkane and the nucleophile attacks from the opposite side.

2,3-dimethylpentane has a total of 7 carbons and 16 hydrogens, giving it the molecular formula C7H16.

2-butyne is an alkyne with the formula C4H6, as it contains a triple bond.

3-methyl-1-butyne has the molecular formula C5H8, as it contains a triple bond.

2,3-dimethylbutane has a total of 7 carbon atoms and 16 hydrogen atoms, giving the formula C7H16.

2-butyne has a triple bond and contains 4 carbons and 6 hydrogens, giving the formula C4H6.

In the complex [Fe(CN)6]3-, each cyanide (CN) has a charge of -1. Therefore, to balance the overall charge of -3, iron must be in the +3 oxidation state.

Werner's theory emphasizes the importance of ligands surrounding a central metal ion, which defines the structure and properties of coordination compounds.

Chemisorption involves stronger interactions and is often irreversible, while physisorption is weaker and reversible.

Addition polymers are primarily formed through a free radical mechanism, where free radicals initiate the polymerization process.

Adsorption can occur through physical or chemical means, but chemical adsorption (chemisorption) involves the formation of a chemical bond between the adsorbate and the surface.

During the electrolysis of aqueous NaCl, chlorine gas is produced at the anode due to the oxidation of chloride ions.

The reaction is an elimination reaction (E2) where sodium ethoxide acts as a strong base, leading to the formation of 2-methylpropene.

Colligative properties depend on the concentration of solute particles in a solution, not their identity.

The addition of a solute decreases the vapor pressure of the solvent, which requires a higher temperature to reach the boiling point.

Intermolecular forces cause real gases to deviate from ideal behavior, especially at high pressures and low temperatures.

Sodium has an atomic number of 11, and its outermost electrons are in the n=3 energy level.

The complete combustion of 2-butyne produces carbon dioxide (CO2) and water (H2O).

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

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

The dehydration of an alcohol typically results in the formation of an alkene.

E1 elimination of 2-bromo-2-methylpropane leads to the formation of 2-methylpropene as the major product.

The E2 elimination of 2-bromobutane primarily yields 2-butene as the product due to the formation of a double bond between the second and third carbons.

The product is toluene sulfonic acid, formed when toluene reacts with sulfuric acid in an electrophilic substitution reaction.

The major product is but-2-ene due to the formation of the more stable alkene through elimination.

The product of the Friedel-Crafts acylation of benzene with acetyl chloride is acetophenone, where an acyl group is introduced to the benzene ring.

The product is acetophenone, formed when benzene reacts with acetyl chloride in the presence of a Lewis acid catalyst.

The product is acetophenone, formed by the acylation of benzene with acetyl chloride.

The product of the Friedel-Crafts acylation of benzene with acetyl chloride is acetophenone, formed by the introduction of the acetyl group onto the benzene ring.

The product is propylbenzene, formed when benzene reacts with 1-bromopropane in the presence of AlCl3, which generates a propyl cation.