Additional Problems 22

Visualizing Chemistry

Problem 22-17

Show the steps in preparing each of the following substances using either a malonic ester synthesis or an acetoacetic ester synthesis:

(a)

(b)

Problem 22-18

Unlike most β-diketones, the following β-diketone has no detectable enol content and is about as acidic as acetone. Explain.

Problem 22-19

For a given α hydrogen atom to be acidic, the C–H bond must be parallel to the p orbitals of the C=O double bond (that is, perpendicular to the plane of the adjacent carbonyl group). Identify the most acidic hydrogen atom in the conformation shown for the following structure. Is it axial or equatorial?

Mechanism Problems

Problem 22-20

Draw the corresponding keto or enol tautomer for each of the following molecules.

(a)

(b)

Problem 22-21

Predict the product(s) and show the mechanism for each of the following reactions:

(a)

(b)

Problem 22-22

Predict the product(s) and show the mechanism for each of the following reactions:

(a)

(b)

Problem 22-23

The following two optically active β-keto acids were decarboxylated under the conditions typically used for the acetoacetic ester synthesis. Will the ketone products be optically active? Explain.

(a)

(b)

Problem 22-24

In the Hell–Volhard–Zelinskii reaction, only a catalytic amount of PBr3 is necessary because of the following equilibrium. Propose a mechanism for formation of the equilibrium.

Problem 22-25

When a ketone is treated with a halogen under acidic conditions, the α-monohalogenated product can be obtained in high yield. Under basic conditions however it is difficult to isolate the monohalogenated product. Explain.

Problem 22-26

Nonconjugated β,γ-unsaturated ketones, such as 3-cyclohexenone, are in an acid-catalyzed equilibrium with their conjugated α,β-unsaturated isomers. Propose a mechanism for the isomerization.

Problem 22-27

2-substituted 2-cyclopentenones can be interconverted with 5-substituted 2- cyclopentenones under basic conditions. Propose a mechanism for this isomerization.

Problem 22-28

Using curved arrows, propose a mechanism for the following reaction, one of the steps in the metabolism of the amino acid alanine.

Problem 22-29

Using curved arrows, propose a mechanism for the following reaction, one of the steps in the biosynthesis of the amino acid tyrosine.

Problem 22-30

One of the later steps in glucose biosynthesis is the isomerization of fructose 6-phosphate to glucose 6-phosphate. Propose a mechanism, using acid or base catalysis as needed.

Problem 22-31

The Favorskii reaction involves treatment of an α-bromo ketone with base to yield a ring- contracted product. For example, reaction of 2-bromocyclohexanone with aqueous NaOH yields cyclopentanecarboxylic acid. Propose a mechanism.

Problem 22-32

Treatment of a cyclic ketone with diazomethane is a method for accomplishing a ring- expansion reaction. For example, treatment of cyclohexanone with diazomethane yields cycloheptanone. Propose a mechanism.

Problem 22-33

The final step in an attempted synthesis of laurene, a hydrocarbon isolated from the marine alga Laurencia glandulifera, involved the Wittig reaction shown. The product obtained, however, was not laurene but an isomer. Propose a mechanism to account for the unexpected results.

Problem 22-34

Amino acids can be prepared by reaction of alkyl halides with diethyl acetamidomalonate, followed by heating the initial alkylation product with aqueous HCl. Show how you would prepare alanine, CH3CH(NH2)CO2H, one of the twenty amino acids found in proteins, and propose a mechanism for acid-catalyzed conversion of the initial alkylation product to the amino acid.

Problem 22-35

Amino acids can also be prepared by a two-step sequence that involves Hell–Volhard– Zelinskii reaction of a carboxylic acid followed by treatment with ammonia. Show how you would prepare leucine, (CH3)2CHCH2CH(NH2)CO2H, and identify the mechanism of the second step.

Problem 22-36

Heating carvone with aqueous sulfuric acid converts it into carvacrol. Propose a mechanism for the isomerization.

Acidity of Carbonyl Compounds

Problem 22-37

Identify all the acidic hydrogens (pKa < 25) in the following molecules:

(a)

(b)

(c)

(d)

(e)

(f)

Problem 22-38

Rank the following compounds in order of increasing acidity:

(a) (b) (c) (d) (e)(f)

Problem 22-39

Write resonance structures for the following anions:

(a)

(b)

(c)

(d)

(e)

Problem 22-40

Base treatment of the following α,β-unsaturated carbonyl compound yields an anion by removal of H+ from the γ carbon. Why are hydrogens on the γ carbon atom acidic?

Problem 22-41

Treatment of 1-phenyl-2-propenone with a strong base such as LDA does not yield an anion, even though it contains a hydrogen on the carbon atom next to the carbonyl group. Explain.

α-Substitution Reactions

Problem 22-42

Predict the product(s) of the following reactions:

(a)

(b)

(c)

(d)

Problem 22-43

Which, if any, of the following compounds can be prepared by a malonic ester synthesis? Show the alkyl halide you would use in each case.

(a) Ethyl pentanoate(b) Ethyl 3-methylbutanoate(c) Ethyl 2-methylbutanoate

(d) Ethyl 2,2-dimethylpropanoate Problem 22-44

Which, if any, of the following compounds can be prepared by an acetoacetic ester synthesis? Explain.

(a)(b) (c)

Problem 22-45

How would you prepare the following ketones using an acetoacetic ester synthesis?

(a)

(b)

Problem 22-46

How would you prepare the following compounds using either an acetoacetic ester synthesis or a malonic ester synthesis?

(a)

(b)

(c)

(d)

Problem 22-47

Which of the following substances would undergo the haloform reaction?

(a) CH3COCH3(b) Acetophenone(c) CH3CH2CHO(d) CH3CO2H(e) CH3C≡N

Problem 22-48

How might you convert geraniol into either ethyl geranylacetate or geranylacetone?

Problem 22-49

Aprobarbital, a barbiturate once used in treating insomnia, is synthesized in three steps from diethyl malonate. Show how you would synthesize the necessary dialkylated intermediate, and then propose a mechanism for the reaction of this intermediate with urea to give aprobarbital.

General Problems

Problem 22-50

One way to determine the number of acidic hydrogens in a molecule is to treat the compound with NaOD in D2O, isolate the product, and determine its molecular weight by mass spectrometry. For example, if cyclohexanone is treated with NaOD in D2O, the product has MW = 102. Explain how this method works.

Problem 22-51

When optically active (R)-2-methylcyclohexanone is treated with either aqueous base or acid, racemization occurs. Explain.

Problem 22-52

Would you expect optically active (S)-3-methylcyclohexanone to be racemized on acid or base treatment in the same way as 2-methylcyclohexanone (Problem 22-51)? Explain.

Problem 22-53

When an optically active carboxylic acid such as (R)-2-phenylpropanoic acid is brominated under Hell–Volhard–Zelinskii conditions, is the product optically active or racemic?

Explain.

Problem 22-54

Fill in the reagents a–c that are missing from the following scheme:

Problem 22-55

Although 2-substituted 2-cyclopentenones are in a base-catalyzed equilibrium with their 5- substituted 2-cyclopentenone isomers, the analogous isomerization is not observed for 2- substituted 2-cyclohexenones. Explain.

Problem 22-56

How would you synthesize the following compounds from cyclohexanone? More than one step may be required.

(a)

(b)

(c)

(d)

(e)

(f)

Problem 22-57

The two isomers cis– and trans-4-tert-butyl-2-methylcyclohexanone are interconverted by base treatment. Which isomer do you think is more stable, and why?

Problem 22-58

The following synthetic routes are incorrect. What is wrong with each?

(a)

(b)

(c)

Problem 22-59

Attempted Grignard reaction of cyclohexanone with tert-butylmagnesium bromide yields only about 1% of the expected addition product along with 99% unreacted cyclohexanone. If D3O+ is added to the reaction mixture after a suitable period, however, the “unreacted” cyclohexanone is found to have one deuterium atom incorporated into it. Explain.

Problem 22-60

Ketones react slowly with benzeneselenenyl chloride in the presence of HCl to yield α– phenylseleno ketones. Propose a mechanism for this acid-catalyzed α-substitution reaction.

Problem 22-61

South American Incas chewed the leaves of the coca bush, Erythroxylon coca, to combat fatigue. Chemical studies of Erythroxylon coca by Friedrich Wöhler in 1862 resulted in the discovery of cocaine, C17H21NO4, as the active component. Basic hydrolysis of cocaine leads to methanol, benzoic acid, and another compound called ecgonine, C9H15NO3. Oxidation of ecgonine with CrO3 yields a keto acid that readily loses CO2 on heating, giving tropinone.

(a) What is a likely structure for the keto acid?

(b) What is a likely structure for ecgonine, neglecting stereochemistry?

(c) What is a likely structure for cocaine, neglecting stereochemistry?

Problem 22-62

The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?

Problem 22-63

Sodium pentothal is a short-acting barbiturate derivative used as a general anesthetic and known in popular culture as a truth serum. It is synthesized like other barbiturates (see the Chemistry Matters at the end of this chapter), using thiourea, (H2N)2C═S, in place of urea.

How would you synthesize sodium pentothal?