Triethyloxonium tetrafluoroborate, (CH₃CH₂)₃O⁺ BF₄^–, is a solid with melting point 91–92°C. Show how this reagent can transfer an ethyl group to a nucleophile (Nuc:⁻) in an S_N2 reaction. What is the leaving group? Why might this reagent be preferred to using an ethyl halide? (Consult Table 6-2)

Draw a perspective structure or a Fischer projection for the products of the following S_N2 reactions.

(e)

Draw a perspective structure or a Fischer projection for the products of the following S_N2 reactions.

(f)

Predict the compound in each pair that will undergo the S_N2 reaction faster.

(c)

(d)

For each pair of compounds, state which compound is the better S_N2 substrate.

c. 2-bromobutane or isopropyl bromide

d. 1-chloro-2,2-dimethylbutane or 2-chlorobutane

e. 1-iodobutane or 2-iodopropane

Explain why a much better yield of primary amine is obtained from the reaction of an alkyl halide with azide ion (^-N₃), followed by catalytic hydrogenation. (Hint: An alkyl azide is not nucleophilic.)

Consider the reaction of 1-bromobutane with a large excess of ammonia (NH₃). Draw the reactants, the transition state, and the products. Note that the initial product is the salt of an amine (RNH₃⁺Br⁻), which is deprotonated by the excess ammonia to give the amine.

Draw a perspective structure or a Fischer projection for the products of the following S_N2 reactions.

(a) trans-1-bromo-3-methylcyclopentane + KOH

(b) (R)-2-bromopentane + KCN

Draw a perspective structure or a Fischer projection for the products of the following S_N2 reactions.

(c)

(d)