For each reaction, give the expected substitution product, and predict whether the ­mechanism will be predominantly first order (SN1) or second order (SN2).
c. 1-iodo-1-methylcyclohexane + ethanol

Predict the major products of the following substitutions.

f.

Chlorocyclohexane reacts with sodium cyanide (NaCN) in ethanol to give cyanocyclohexane. The rate of formation of cyanocyclohexane increases when a small amount of sodium iodide is added to the solution. Explain this acceleration in the rate.

Draw perspective structures or Fischer projections for the substitution products of the following reactions.

(b)

a. Optically active 2-bromobutane undergoes racemization on treatment with a solution of KBr. Give a mechanism for this racemization.

b. In contrast, optically active butan-2-ol does not racemize on treatment with a solution of KOH. Explain why a ­reaction like that in part (a) does not occur.

The following reaction takes place under second-order conditions (strong nucleophile), yet the structure of the product shows rearrangement. Also, the rate of this reaction is several thousand times faster than the rate of substitution of ­hydroxide ion on 2-chlorobutane under similar conditions. Propose a mechanism to explain the enhanced rate and ­rearrangement observed in this unusual reaction. (“Et” is the abbreviation for ethyl.)

Using the given starting material, any necessary inorganic reagents and catalysts, and any carbon-containing compounds with no more than three carbons, indicate how each of the following compounds can be prepared:

a.

For each reaction, give the expected substitution product, and predict whether the ­mechanism will be predominantly first order (S_N1) or second order (S_N2).

a. 2-chloro-2-methylbutane + CH₃COOH

b. isobutylbromide + sodium methoxide

Show how you might use S_N2 reactions to convert 1-chlorobutane into the following compounds.

a. butan-1-ol