91Ó°ÊÓ

Farnesyl diphosphates are familiar by another name, farnesyl pyrophosphate. They serve as intermediates in the preparation of terpenes and terpenoids.

Several biological reactions utilize allylic carbocations that are generated from diphosphates as intermediates. A new carbon-carbon bond is created in this biological process.

In biological reactions, allylic carbocations serve as intermediates for the formation of farnesyl diphosphate.

The first step of this reaction is the generation of allylic carbocation by losing the diphosphate group. The second step is the nucleophilic attack of isopentyl diphosphate leading to the formation of a new bond.

The third step is deprotonation leading to the final product.

The reaction can be given as:

Reaction of isopentyl diphosphate leading to farnesyl diphosphate

Hence the structure of X can be given as:

Structure of X