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Chapter 6: 46P-b (page 330)

Question: Using cyclohexane as one of your starting materials, show how you would synthesize the following compounds.

b)

Short Answer

Expert verified

b) The synthesis reaction of given compound is as follows,

Step by step solution

01

Concept

The bromination reaction is the process by which one or more bromine atoms are added to a chemical. Halogen reaction is also include bromination reactions.

Any chemical reaction is referred to as a substitution reaction if one functional group is replaced or substituted with different functional group.

02

Step 2:

In the 1st step cyclohexane is converted to cyclohexyl bromide (Refer:971371-6-46P-a)

In this process of turning cyclohexyl bromide into Cyclohexanol, bromine atoms are substituted via SN1 mechanism, and silver ions are employed as silver bromide by getting rid of the bromide anion. The presence of water causes the hydroxyl group to bind the ring.

03

Step 3:

The synthesis reaction of given compound is as follows,

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Most popular questions from this chapter

Give systematic (IUPAC) names for the following compounds.

Give two syntheses for (CH3)2CH-OCH3, and explain which synthesis is better.

Propose a mechanism involving a hydride shift or alkyl shift for each solvolysis reaction. Explain howeach rearrangement forms a more stable intermediate.

(a)

(b)

(c)

(d)

Predict the major product of the following reaction, and give a mechanism to support your prediction.

For each pair of compounds, predict which one has the higher molecular dipole moment, and explain your reasoning.

(a) ethyl chloride or ethyl iodide

(b) 1-bromopropane or cyclopropane

(c) cis-2,3-dibromobut-2-ene or trans-2,3-dibromobut-2-ene

(d) cis-1,2-dichlorocyclobutane or trans-1,3-dichlorocyclobutane.
See all solutions

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