Answered: Show how you would convert…

Show how you would convert 2-methylcyclopentanol to the following products. Any of these products may be used as thereactant in any subsequent part of this problem.(a) 1-methylcyclopentene

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter22: Carbonyl Alpha-substitution Reactions

Section22.SE: Something Extra

Problem 26MP: Nonconjugated , -unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium...

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Concept explainers

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.

Question

Show how you would convert 2-methylcyclopentanol to the following products. Any of these products may be used as the
reactant in any subsequent part of this problem.
(a) 1-methylcyclopentene

Expert Solution

Step 1

The functional group present in 2-methylcyclopentanol is alcohol that is -OH group. There is the conversion of 2-methylcyclopentanol to 1-methylcyclopentene. Here there is the conversion from alcohol to an alkene. It can be carried out by heating alcohol with an acid.

Step 2

The structure of 2-methylcyclopentanol is given below:

The structure of 1-methylcyclopentene is given below:

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