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Question: Hydrocarbons like benzene are metabolized in the body to arene oxides, which rearrange to form phenols. This is an example of a general process in the body, in which an unwanted compound (benzene) is converted to a more water-soluble derivative called a metabolite, so that it can be excreted more readily from the body.

a. Classify each of these reactions as oxidation, reduction, or neither.

b. Explain why phenol is more water soluble than benzene. This means that phenol dissolves in urine, which is largely water, to a greater extent than benzene.

Short Answer

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Answer

  1. The conversion of benzene to arene oxide is an oxidation reaction. The conversion of arene oxide to phenol is neither a reduction reaction nor an oxidation reaction.
  2. Phenol is more soluble in water because it is a polar compound with an O-H bond that binds with the molecules of water.

Step by step solution

01

Oxidation reactions

Oxidation reactions are characterized either by the gain of an electronegative element or the loss of an electropositive element.

02

Reduction reactions

Reduction reactions are characterized either by the gain of an electropositive element or the loss of an electronegative element.

03

Solubility

Like dissolves like;polar solvents dissolve only polar compounds into them. In contrast, non-polar solvents dissolve only non-polar compounds.

For example, water (polar solvent) dissolves ethanol, salts, some bases, and acids. On the contrary, benzene (non-polar solvent) can dissolve only non-polar substances such as some ketones, ethers, and substituted benzene compounds.

04

Types of reaction in the given compounds

a. In the reaction of benzene to form arene oxide in step [1], two C-O bonds are added to the benzene ring. Hence, benzene is said to be oxidized.

In the reaction of arene oxide to form phenol in step [2], a C-O bond and a C-H bond are broken. Hence, this reaction is neither reduction nor oxidation.

Types of Reactions

b. Phenol is a polar compound with an O-H bond. These O-H groups bind with the water molecules. Hence, phenol is more soluble in water, a polar solvent, than in benzene, which is a non-polar solvent.

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Most popular questions from this chapter

Question: Consider rotation around the carbon-carbon bond in 1,2-dichloroethane (ClCH2CH2Cl).

a.Using Newman projections, draw all of the staggered and eclipsed conformations that result from rotation around this bond.

b. Graph energy versus dihedral angle for rotation around this bond.

Question: Read Appendix B on naming bicyclic compounds. Then give the IUPAC name for each of the following compounds.

a.

b.

c.

d.

Question: Answer the following questions about compounds A–D.

a. How are the compounds in each pair related? Choose from constitutional isomers, stereoisomers, or identical molecules: A and B; A and C; B and D.

b. Label each compound as a cis or trans isomer.

c. Draw B as a hexagon with wedges and dashed wedges to show the stereochemistry of substituents.

d. Draw a stereoisomer of A as a hexagon using wedges and dashed wedges to show the orientation of substituents.

Question: Using the cyclohexane with the C’s numbered as shown, draw a chair form that fits each description.

a. The ring has an axial CH3group at C1 and an equatorial OH on C2.

b. The ring has an equatorial CH3group on C6 and an axial OH group on C4.

c. The ring has equatorial OH groups on C1, C2, and C5.

Question: For each compound drawn below:

a. Draw representations for the cis and trans isomers using a hexagon for the six membered ring, and wedges and dashed wedges for substituents.

b. Draw the two possible chair conformations for the cis isomer. Which conformation, if either, is more stable?

c. Draw the two possible chair conformations for the trans isomer. Which conformation, if either, is more stable?

d. Which isomer, cis or trans, is more stable and why?

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