Structure 2.2.12—Benzene, C6H6, is an important example of a molecule that has resonance. Discuss the structure of benzene from physical and chemical evidence.

Draw the structure of one other isomer of xylene which retains the benzene ring.

Draw the structure of one other isomer of xylene which retains the benzene ring.

Draw the structure of one other isomer of xylene which retains the benzene ring.

Draw the structure of one other isomer of xylene which retains the benzene ring.

Draw the structure of one other isomer of xylene which retains the benzene ring.

Draw the structure of one other isomer of xylene which retains the benzene ring.

The minor product, C₆H₅–CH₂–CH₂Br, can exist in different conformational forms (isomers).

Outline what this means.

The minor product, C₆H₅–CH₂–CH₂Br, can exist in different conformational forms (isomers).

Outline what this means.

The minor product, C₆H₅–CH₂–CH₂Br, can exist in different conformational forms (isomers).

Outline what this means.

The minor product, C₆H₅–CH₂–CH₂Br, can exist in different conformational forms (isomers).

Outline what this means.

The minor product, C₆H₅–CH₂–CH₂Br, can exist in different conformational forms (isomers).

Outline what this means.

The minor product, C₆H₅–CH₂–CH₂Br, can exist in different conformational forms (isomers).

Outline what this means.

Draw the structure of one other isomer of xylene which retains the benzene ring.

Draw the structure of one other isomer of xylene which retains the benzene ring.

Draw the structure of one other isomer of xylene which retains the benzene ring.

Draw the structure of one other isomer of xylene which retains the benzene ring.

Draw the structure of one other isomer of xylene which retains the benzene ring.

Draw the structure of one other isomer of xylene which retains the benzene ring.

Draw the structure of the conjugate base of benzoic acid showing all the atoms and all the bonds.

Draw the structure of the conjugate base of benzoic acid showing all the atoms and all the bonds.

Draw the structure of the conjugate base of benzoic acid showing all the atoms and all the bonds.

The pH of an aqueous solution of benzoic acid at 298 K is 2.95. Determine the concentration of hydroxide ions in the solution, using section 2 of the data booklet.

The pH of an aqueous solution of benzoic acid at 298 K is 2.95. Determine the concentration of hydroxide ions in the solution, using section 2 of the data booklet.

The pH of an aqueous solution of benzoic acid at 298 K is 2.95. Determine the concentration of hydroxide ions in the solution, using section 2 of the data booklet.

Formulate the equation for the complete combustion of benzoic acid in oxygen using only integer coefficients.

Formulate the equation for the complete combustion of benzoic acid in oxygen using only integer coefficients.

Formulate the equation for the complete combustion of benzoic acid in oxygen using only integer coefficients.

Suggest how benzoic acid, M_r = 122.13, forms an apparent dimer, M_r = 244.26, when dissolved in a non-polar solvent such as hexane.

Suggest how benzoic acid, M_r = 122.13, forms an apparent dimer, M_r = 244.26, when dissolved in a non-polar solvent such as hexane.

Suggest how benzoic acid, M_r = 122.13, forms an apparent dimer, M_r = 244.26, when dissolved in a non-polar solvent such as hexane.