Question

Devise a three‑step synthesis of the product from 1‑methylcyclohexene

Answer 1

The three step synthesis of the product from 1-methyl cyclohexane includes the addition of;

• C6H5CO3H in CH2Cl2
• C6H5Li in ether
• PCC in CH2Cl2.

Three step synthesis from 1 methyl cyclohexene

The three steps reaction involves the use of Reagannts such as;

• Reagent 1: C6H5CO3H in CH2Cl2.
• Reagent 2: C6H5Li in ether.
• Reagent 3: PCC in CH2Cl2.

Each step in the synthesis is arranged in the order:

• Step 1: Epoxide formation
• Step 2: Nucleophilic addition
• Step 3: Oxidation of OH group.

Read more on three step synthesis;

brainly.com/question/14596275

Answer 2

Three step synthesis of the product from 1‑methylcyclohexene includes epoxide formation, nucleophilic attack and oxidation of -OH group.

What is synthesis reaction?

Synthesis reactions are those reactions in which formation of new product takes place by the rearrangement or combination of reactant molecules.

Given question is incomplete so the complete pic of the question is attached below. In the given reaction reagents 1, 2 and 3 are used is C₆H₅CO₃H in CH₂Cl₂, C₆H₅Li in ether and PCC in CH₂Cl₂ respectively.

In the tree step synthesis process, in the first step formation of epoxide takes place, in the second step attack of nucleophile on epoxide takes place and finally in the third step oxidation of hydroxyl group to ketone group takes plce.

Hence 3 step synthesis includes epoxide formation, nucleophilic attack and oxidation of -OH group.

To know more about three step synthesis, visit the below link:

brainly.com/question/14596275

#SPJ4