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Chapter 10: Q10-25E-a (page 308)

How would you prepare the following compounds, starting with cyclopentene and any other reagents needed? (a) Chlorocyclopentane.

Short Answer

Expert verified

Chlorocyclopentane can be formed in the following way:

Step by step solution

01

Chlorination 

It means substitution of one hydrogen from the reactant, so that halogen atom can be added there.

02

Alkyl halide

Alkyl halides are also known as haloalkanes or halogenoalkanes. They contains one or more halogen substituents i.e. –Br, -Cl,-I,-F.

03

Preparation of chlorocyclopentane

The desired product chlorocyclopentane can be prepared by chlorinating cyclopantene.

The reaction is as follows:

Preparation of chlorocyclopentane

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Most popular questions from this chapter

Name the following alkyl halides:

How would you prepare the following compounds, starting with cyclopentene and any other reagents needed? (d) Cyclopentanol.

Predict the product and provide the entire catalytic cycle for theSuzuki–Miyaura reactions below.

Draw three resonance forms for the cyclohexadienyl radical.

Cyclohexadienyl radical

Question: How strong a base would you expect a Grignard reagent to be? Look at Table 9-1 on page 276, and predict whether the following reactions will occur as written. (The pKaof NH3is 35.)
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