91Ó°ÊÓ

In the first step, the given starting material cyclopentylmethanol is treated with ${\mathrm{PBr}}_3$to form a P-O bond by displacing bromide ion. In the complex cation, the oxygen atom in the alcohol group bears a positive on it and making it as a good leaving group.This process is known as activation. The bromide ion attacks the carbon atom through${\mathrm{S}}_{\mathrm{N}}2$mechanism to form a new carbon-bromine bond as shown below.

In the second step, (bromomethyl)cyclopentane reacts with$\mathrm{NaCH}$to give 2-

cyclopentylacetonitrile through an${\mathrm{S}}_{\mathrm{N}}2$nucleophilic substitution pathway. In the third

step, the hydrolysis of 2- cyclopentylacetonitrile in the presence of aqueous acid

$\left({\mathrm{H}}_3{\mathrm{O}}^{+}\right)$to produce 2-cyclopentylacetic acid as shown below

In the fourth step, 2-cyclopentylacetic acid is successfully converted to 2-

cyclopentyl-1-ethanol by using the strong reducing agent,${\mathrm{LiAIH}}_4$This above

said reaction is drawn as follows.