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Question: Classify each transformation as an oxidation, reduction, or neither.

a.

b.

c.

d.

Short Answer

Expert verified

Answer

  1. Oxidation takes place due to an increase in the number of carbon-oxygen bonds.
  2. Reduction takes place due to an increase in the number of C-H bonds.
  3. There is neither reduction nor oxidation in this reaction because the number of C-O and C-H bonds remains the same.
  4. Reduction takes place due to an increase in the number of C-H bonds.

Step by step solution

01

Meaning of oxidation and reduction

Oxidation refers to the process when an increase in the number of C-Z bonds or a decrease in the number of C-H bonds takes place. Z refers to elements that are more electronegative than the carbon atom; for example, oxygen, nitrogen, and halogens.

Reduction is a process when a decrease in the number of C-Z bonds and an increase in the number of C-H bonds takes place.

The replacement of C-H bonds with C-Z decreases the electron density around the carbon atom, thereby resulting in oxidation.

02

Step 2:Classification of the reactions into oxidation and reduction

a. In the following reaction, the formation of a new C-O bond has occurred. Since oxygen is more electronegative than carbon, it causes a decrease in the electron density around carbon. Hence, oxidation takes place in the following reaction:

Oxidation takes place

b. In the following reaction, reduction takes place because of the decrease in the number of C-O bonds.

Reduction takes place

The carbon atom in the above reaction has formed two new C-H bonds after removing a double bond with an oxygen atom.

c. In this reaction, there is no overall change in the number of C-H and C-O bonds. Therefore, there is neither oxidation nor reduction taking place in the given reaction.

Neither oxidation nor reduction takes place

d. There is a decrease in the number of C-O bonds, and an increase in the number of C-H bonds. Therefore, reduction takes place in the following reaction:

Reduction takes place

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Most popular questions from this chapter

Question: Draw a chair conformation of cyclohexane with one CH3CH2 group and one role="math" localid="1648542173942" CH3 group that fits each description.

  1. a 1,1-disubstituted cyclohexane with an axial role="math" localid="1648542231267" CH3CH2 group
  2. a cis-1,2-disubstituted cyclohexane with an axial role="math" localid="1648542270917" CH3 group
  3. a trans-1,3-disubstituted cyclohexane with an equatorial CH3 group
  4. a trans-1,4-disubstituted cyclohexane with an equatorialCH3CH2 group

Question: Answer the following questions about compound A, which contains a -CH3group and OH group bonded to the carbon skeleton that consists of three six-membered rings in the conformation shown.

a. Are the -CH3and OH groups oriented cis or trans to each other?

b. Is a substituent on localid="1648626189057" Cathat is cis to the CH3 group located in the axial or equatorial position?

c. Is an equatorial Br at Cboriented cis or trans to the OH group?

d. Is the H atom on Cclocated cis or trans to the OH group?

e. Is a substituent on Cdthat is trans to the OH group located in the axial or equatorial position?

Question: a.Draw the three staggered and three eclipsed conformations that result from rotation around the bond labeled in red using Newman projections. b. Label the most stable and least stable conformation.

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: Haloethanes(CH3CH2X,X=Cl,Br,I) have similar barriers to rotation (13.4–15.5 kJ/mol) despite the fact that the size of the halogen increases, role="math" localid="1648639622891" Cl→Br→I. Offer an explanation.

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