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Chapter 8: 8-110P (page 381)

Identify the product of the following reaction. (Hint:It has a fused bicyclic ring.)

Short Answer

Expert verified

The product of the following reaction is:

Step by step solution

01

Step 1:Diels-Alder reaction:

The cyclo addition reaction of diene with a dienophile yields a cyclo hexene.

Example: 1,3 butadiene undergoes cyclo addition reaction with ethylene (diene) to form a cyclohexene. This reaction takes place through a six membered cyclic transition state.

02

Final answer

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Most popular questions from this chapter

a. In what direction is the dipole moment in fulvene? Explain.

b. In what direction is the dipole moment in calicene? Explain.

What orbitals contain the electrons represented as lone pairs in the structures of quinoline, indole, imidazole, purine, and pyrimidine?

The experiment shown next and discussed in Section 8.13 shows that the proximity of the chloride ion to C−2 in the transition state causes the 1,2−addition product to be formed faster than the 1,4−addition product.

a. Why was it important for the investigators to know that the preceding reaction was being carried out under kinetic control?

b. How could the investigators know that the reaction was being carried out under kinetic control?

The following equilibrium is driven to the right if the reaction is carried out in the presence of maleic anhydride (see Problem 106). What is the function of maleic anhydride?

Explain why the following compounds are not optically active:

a. the product obtained from the reaction of 1,3-butadiene with cis-1,2-dichloroethene

b. the product obtained from the reaction of 1,3-butadiene with trans-1,2-dichloroethene
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