Benzylbromide

Bromoethane

Cyclopentylbromide

3-methyl-3-iodopentane

Cis-2-bromo-1-methylcyclohexane

Benzylbromide

Bromoethane

Cyclopentylbromide

3-methyl-3-iodopentane

Cis-2-bromo-1-methylcyclohexane

I

II

III

IV

V

I

II

III

IV

V

All of these are true statements

SN1 reactions follow a 2-step mechanism; SN2 reactions follow a 1-step mechanism

Acetate is a better nucleophile than acetic acid

The more hindered a strong base is, the more likely it is to produce an E2 reaction

In the absence of heat, strong bases, and good nucleophiles, tertiary alkyl halides will react via the SN1 mechanism

All of these are true statements

SN1 reactions follow a 2-step mechanism; SN2 reactions follow a 1-step mechanism

Acetate is a better nucleophile than acetic acid

The more hindered a strong base is, the more likely it is to produce an E2 reaction

In the absence of heat, strong bases, and good nucleophiles, tertiary alkyl halides will react via the SN1 mechanism

No reaction.

More than one of these.

No reaction.

More than one of these.

Tertiary, secondary, primary, methyl

Methyl, primary, secondary, tertiary

Primary, secondary, tertiary, methyl

Methyl, tertiary, secondary, primary

The stability of a carbocation depends only on the solvent of the solution

None of these