Benzyl ethers make excellent protecting groups according to the general scheme shown here.
(a) How would you protect the 1° alcohol as a benzyl ether in the first step?

Mullins 1st Edition
Ch. 13 - Alcohols, Ethers and Related Compounds: Substitution and Elimination
Problem 112
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Benzyl ethers make excellent protecting groups according to the general scheme shown here.
(a) How would you protect the 1° alcohol as a benzyl ether in the first step?
Thiols are prone to dimerize through the formation of a disulfide bond in a reaction that stylists use to induce permanent curls in hair. What type of reagent would you use to effect this transformation?
Triphenylphosphine and iodine can be used to convert alcohols to iodoalkanes. Suggest a mechanism for this reaction. [Triphenylphosphine first acts as a nucleophile in this reaction.]
A chemist attempted the reaction below, one we introduce in Chapter 17, expecting the reaction between a strong nucleophile and a ketone in water to give an alkoxide product.
(a) Why did the reaction fail?
(b) How could the reaction conditions be changed to give a successful reaction?
Another method for converting alcohols to chloroalkanes makes use of chlorotrimethylsilane (TMSCl) and DMSO. Suggest a mechanism for this reaction to form (a) a 1° chloroalkane and (b) a 3° chloroalkane. [The reaction begins by the reaction of DMSO and TMSCl and is analogous to the Swern oxidation.]
We explain in Chapter 24 that bisphenols can be oxidized to quinones.
(a) Calculate the oxidation numbers of C1 and C₂ in going from reactant to product.
(b) Provide a mechanism for this transformation. [The reaction begins like the alcohol oxidations of Section 13.9.]