Question: Identify the common name for each of
Identify the common name for each of the following compounds:
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(а) (Б) OH (c) H OH (d) HO он
> Enaminoesters (also called vinylogous carbamates), such as compound 4 below, can serve as building blocks in the synthesis of nitrogen heterocycles. Compound 4 was prepared from compound 1 in a one-pot method (the entire transformation took place in one
> Piperazinone derivatives, such as compound 4, are being investigated for their potential use in the treatment of migraines as well as a variety of other diseases, including hypertension and sepsis. The following two-step synthetic procedure was developed
> Dogs are used by police and emergency personnel to detect a variety of things, including drugs, explosives, and humans (both as missing persons and as deceased bodies). Canines that are trained to detect human remains (aka, cadaver dogs) can be trained u
> Draw the structure of each of the following compounds: a. Cyclohexylmethylamine b. Tricyclobutylamine c. 2,4-Diethylaniline d. (1R,2S)-2-Methylcyclohexanamine e. ortho-Aminobenzaldehyde
> Assign a name for each of the following compounds: NH2 (a) NH2 (b) (c) NH2 но, NH2 (d) (e) (f)
> When the following compound is treated with concentrated HCl at 100ºC for several hours, hydrolysis occurs, producing one of the 20 naturally occurring amino acids. Identify which one. H,N Ine
> We saw in Section 25.6 that DCC can be used to form a peptide bond. We explored the mechanism, and we saw that DCC activates the COOH group so that it readily undergoes nucleophilic acyl substitution. An alternative method for activating a COOH group inv
> Proton NMR spectroscopy provides evidence for the restricted rotation of a peptide bond. For example, N,N dimethylformamide exhibits three signals in its proton NMR spectrum at room temperature. Two of those signals are observed upfield, at 2.9 and 3.0
> Compound A is a D-aldopentose. When treated with sodium borohydride, compound A is converted into an alditol that exhibits three signals in its 13C NMR spectrum. Compound A undergoes a Kiliani–Fischer synthesis to produce two aldohexoses, compounds B and
> Compound X is a d-aldohexose that can adopt a β-pyranose form with only one axial substituent. Compound X undergoes a Wohl degradation to produce an aldopentose, which is converted into an optically active alditol when treated with sodium borohydride. Fr
> When optically active (S)-2-methylcyclopentanone is treated with aqueous base, the compound loses its optical activity. Explain this observation and draw a mechanism that shows how racemization occurs.
> A carboxylic acid with the molecular formula C5H10O2 is treated with thionyl chloride to give compound A. Compound A has only one signal in its 1 H NMR spectrum. Draw the structure of the product that is formed when compound A is treated with excess ammo
> Draw a plausible mechanism for the following transformation: te H,0 * но
> Using acetonitrile (CH3CN) and CO2 as your only sources of carbon atoms, identify how you could prepare each of the following compounds: OH OH он OH (a) (b) (c) (d)
> Starting with benzene and using any other reagents of your choice, devise a synthesis for acetaminophen: но Acetaminophen (Tylenol) エーZ
> Propose an efficient synthesis for each of the following transformations: OH (a) `NH (b) (c) S. (d) OMe H. COOH (e) OH
> meta-Hydroxybenzoyl chloride is not a stable compound, and it polymerizes upon preparation. Show a mechanism for the polymerization of this hypothetical compound.
> Identify what monomers you would use to produce the following polymer: Zーエ Zーエ Zーエ Zーエ
> Draw the structure of the polymer produced when the following two monomers are allowed to react with each other: OH CI но
> Dexon (below) is a polyester that is spun into fibers and used for surgical stitches that dissolve over time, eliminating the need for a follow-up procedure to remove the stitches. The ester groups are slowly hydrolyzed by enzymes present in the body, an
> Pivampicillin is a penicillin prodrug: The prodrug ester group (in red) enables a more rapid delivery of the prodrug to the bloodstream, where the ester group is subsequently hydrolyzed by enzymes, releasing the active drug. a. Draw the structure of th
> When 2-hepten-4-one is treated with LDA, a proton is removed from one of the gamma (γ) positions. Identify which γ position is deprotonated and explain why the γ proton is the most acidic proton in the compound.
> Draw the structure of the diol that is produced when the following carbonate is heated under aqueous acidic conditions: H20 ? O: Heat
> Ethyl trichloroacetate is significantly more reactive toward hydrolysis than ethyl acetate. Explain this observation.
> Draw a plausible mechanism for each of the following transformations: -он Pyridine (a) 1) NaOH O. OH (Ь) 21 H,0 HO но OH 1) NAOH 2) H,0* HO (c) CI H,N-NH, Excess pyridine .CI H. (d) 1) Excess EtMgBr 2) H,0 OH (e)
> Aspartame (below) is an artificial sweetener used in diet soft drinks and is marketed under many trade names, including Equal and Nutrasweet. In the body, aspartame is hydrolyzed to produce methanol, aspartic acid, and phenylalanine. The production of ph
> Benzyl acetate is a pleasant-smelling ester found in the essential oil of jasmine flowers and is used in many perfume formulations. Starting with benzene and using any other reagents of your choice, design an efficient synthesis for benzyl acetate. B
> Fluphenazine is an antipsychotic drug that is administered as an ester prodrug via intramuscular injection: The hydrophobic tail of the ester is deliberately designed to enable a slow release of the prodrug into the bloodstream, where the prodrug is rap
> Phosgene is highly toxic and was used as a chemical weapon in World War I. It is also a synthetic precursor used in the production of many plastics. a. When vapors of phosgene are inhaled, the compound rapidly reacts with any nucleophilic sites present
> When acetic acid is treated with isotopically labeled water (18O, shown in red) in the presence of a catalytic amount of acid, it is observed that the isotopic label becomes incorporated at both possible positions of acetic acid. Draw a mechanism that ac
> Predict the products that are formed when diphenyl carbonate is treated with excess methyl magnesium bromide. 1) Excess MeMgBr 2) H0"
> DEET is the active ingredient in many insect repellants, such as OFFTM. Starting with meta-bromotoluene and using any other reagents of your choice, devise an efficient synthesis for DEET. Br ?. N,N-Diethyl-m-toluamide (DEET) m-Bromotoluene
> Draw the enolate that is formed when each of the following compounds is treated with LDA: (a) H. (b) OEt (c)
> Identify reagents that can be used to accomplish each of the following transformations: H. OR *NH, | -
> When methyl benzoate bears a substituent at the para position, the rate of hydrolysis of the ester group depends on the nature of the substituent at the para position. Apparently, a methoxy substituent renders the ester less reactive, while a nitro subst
> Propose an efficient synthesis for each of the following transformations: Br (a) OH (b) Br (c) Br (d)
> Starting with benzene and using any other reagents of your choice, show how you would prepare each of the following compounds: OH of 'N. (а) (b) он (c) (d) エーZ
> Identify the reagents you would use to convert 1-bromopentane into each of the following compounds: a. Pentanoic acid b. Hexanoic acid c. Pentanoyl chloride d. Hexanamide e. Pentanamide f. Ethyl hexanoate
> Determine the structures of compounds A through F: но. Na,Cr,0, OH *osH xs NH, B A 1) LIAI(OR);H 2) H20 [H*] EIOH 오
> Identify the carboxylic acid and the alcohol that are necessary in order to make each of the following compounds via a Fischer esterification: (a) (Б)
> Predict the major product(s) for each of the following reactions: 1) xs LIAIH OH 2) H,0 ? 1) SOCI, 2) xs (CH),NH ? Он (b) ? NH, (c) 1) H,0 OMe 2) CH,COCI, pyridine ? (d) OMe 1) DIBAH 2) H,0 LOH ? (f) Pyridine (h)
> Predict the major product(s) formed when cyclopentanecarboxylic acid is treated with each of the following reagents: a. SOCl2 b. LiAlH4 (excess), followed by H2O c. NaOH d. [H+], EtOH
> Predict the major product(s) formed when hexanoyl chloride is treated with each of the following reagents: a. CH3CH2NH2 (excess) b. LiAlH4 (excess), followed by H2O c. CH3CH2OH, pyridine d. H2O, pyridine e. C6H5CO2Na f. NH3 (excess) g. Et2CuLi h.
> Ethyl acetoacetate has three enol isomers. Draw all three.
> Careful measurements reveal that para-methoxybenzoic acid is less acidic than benzoic acid, while meta-methoxybenzoic acid is more acidic than benzoic acid. Explain these observations.
> Identify the reagents you would use to convert each of the following compounds into pentanoic acid: a. 1-Pentene b. 1-Bromobutane
> Identify the reagents you would use to convert pentanoic acid into each of the following compounds: a. 1-Pentanol b. 1-Pentene c. Hexanoic acid
> Draw and name all constitutionally isomeric acid chlorides with the molecular formula C4H7ClO. Then provide a systematic name for each isomer.
> Draw the structures of eight different carboxylic acids with the molecular formula C6H12O2. Then, provide a systematic name for each compound and identify which three isomers exhibit chiral centers.
> Identify a systematic (IUPAC) name for each of the following compounds: он NH2 (а) (b) (c) (d) (e) CH3(CH2)CO2H (f) CH;(CH,);COCI (g) CH,(CH,),CONH2
> Malonic acid has two acidic protons: The pKa of the first proton (pK1) is measured to be 2.8, while the pKa of the second proton (pK2) is measured to be 5.7. a. Explain why the first proton is more acidic than acetic acid (pKa=4.76). b. Explain why th
> Rank each set of compounds in order of increasing acidity: .COOH COOH COOH .COOH .COOH Вг O,N HC (a) Br Br HO. он OH Br (b)
> Compound A has the molecular formula C9H8O2 and exhibits a strong signal at 1740 cm−1 in its IR spectrum. Treatment with two equivalents of LiAlH4 followed by water gives the following diol. Identify the structure of compound A. OH
> Draw the enol of each of the following compounds and identify whether the enol exhibits a significant presence at equilibrium. Explain. (a) (b) (c)
> α-Bisabolol is the primary constituent of the essential oil of the chamomile plant. It has a long history of use in cosmetics due to its anti-inflammatory and skin-soothing properties. One laboratory synthesis involved the conversion of com
> Propose an efficient synthesis for each of the following transformations: OH Br он (a) (b) CN
> Juvabione is produced by fir trees of the genus Abies and is known to inhibit insect reproduction and growth, thereby offering the trees some protection from insect infestations. One laboratory synthesis of juvabione involved the conversion of compound 1
> Identify reagents that will accomplish each of the following transformations: HO. NH2 > (a) OMe (b) OEt NH2 > (c) (d) CN OH (e) (f) он OEt NH2 H. (h) CN .CN HO. HO, (i)
> Propose a mechanism for the following transformation: NH2 CN H,O Heat
> Identify reagents that can be used to achieve each of the following transformations: CN CI (a) OH Br (b)
> Predict the major product(s) for each of the following reactions: CN 1) xs LIAIH, 2 H0 ? (a) 1) NaCN 2) MeMgBr 3) H,0 ? Br (6) CN 1) EIMgBr ? 2) H,O 3) LIAIH, 4) H,0 (c) CN H,0 ? heat (d)
> Propose a mechanism for each of the following transformations: H,0 H OH Нeat (a) NaOH H. O Na Heat (b) Z-I
> Identify reagents that can be used to achieve the following transformation: NH2
> Predict the major product(s) for each of the following reactions: 1) Excess LIAIH, NH, 2) H0 ? (a) ? CI Excess NH, (b) `NH2 H,0 ? Heat (c)
> Rank the following compounds in terms of increasing acidity: он
> Draw the enolate ion that is formed when each of the following compounds is treated with sodium ethoxide. In each case, draw all resonance structures of the enolate ion and predict whether a substantial amount of starting ketone will be present together
> Propose a mechanism for the following transformation: H,0 но OH
> Predict the major product(s) for each of the following reactions: 1) xs LIAIH, 2) H0 1) xs EtMgBr 2) H,0 ? 1) xs LIAIH, 2) H0 ? OMe OMe (a) (b) (c) OE! H,0 ? HO, 1) NaOH 2) Etl ? 1) xs EtMger 2) H,0 ? (d) (e) (f)
> Identify reagents that can be used to accomplish each of the following transformations: он OEt (a) OEt (b)
> In this section, we have seen three ways to achieve the following transformation. Identify the reagents necessary for all three methods. OH OEt
> Predict the major product(s) for each of the following reactions: -OH .O. (xs) (a) (b) OH ? ? (c) (d) (xs) エーズ エーZ
> Propose a mechanism for the following transformation: .CI 1) xs EIMgBr 2) conc. H,SO, heat
> Identify reagents that can be used to achieve the following transformation: OH
> Predict the major product(s) for each of the following reactions: 1) xs LIAIH, 2) H,0 ? 1) xs PhMgBr 2) H,0 1) LIAI(OR),H ? CI 2) EIMgBr 3) Н,О (b) (c) OH N-H "CI 1) El,CuLi ? CI 2) LIAIH, 3) H,0 Pyridine (two equivalents) (e) (f)
> Chlorocatechelin A was isolated from a bacterial culture, but it had to be synthesized in the laboratory in order to obtain enough pure material for the study of its antimicrobial activity. Shown below is the first step of a 15-step synthesis of chloroca
> Propose a plausible mechanism for each of the following transformations. These reactions will all appear later in this chapter, so practicing their mechanisms now will serve as preparation for the rest of this chapter: NH, O Na NH2 (a) (Ь) MEOH (c) H
> Draw resonance structures for the conjugate base that is produced when each of the following compounds is treated with sodium ethoxide: CN OEt (a) OEt (b) (c)
> Draw a structure for each of the following compounds: a. Dimethyl oxalate b. Phenyl cyclopentanecarboxylate c. N-Methylpropionamide d. Propionyl chloride
> Provide a name for each of the following compounds: (b) (c) (d) (f) (h) (1)
> Identify the reagents you would use to achieve each of the following transformations: Br HO. HO. (b)
> Identify the reagents you would use to perform the following transformations: a. Ethanol → Acetic acid b. Toluene → Benzoic acid c. Benzene → Benzoic acid d. 1-Bromobutane → Pentanoic acid e. Ethylbenzene → Benzoic acid f. Bromocyclohexane → Cycloh
> Rank each set of compounds in order of increasing acidity: a. 2,4-Dichlorobutyric acid 2,3-Dichlorobutyric acid 3,4-Dimethylbutyric acid b. 3-Bromopropionic acid 2,2-Dibromopropionic acid 3,3-Dibromopropionic acid
> Acetic acid was dissolved in a solution buffered to a pH of 5.76. Determine the ratio of the concentrations of acetate ion and acetic acid in this solution. Which species predominates under these conditions?
> When formic acid is treated with potassium hydroxide (KOH), an acid-base reaction occurs, forming a carboxylate ion. Draw a mechanism for this reaction and identify the name of the carboxylate salt.
> Based on your answer to the previous question, would you expect meta-hydroxyacetophenone to be more or less acidic than para-hydroxyacetophenone? Explain your answer. но. но meta-Hydroxyacetophenone para-Hydroxyacetophenone
> Consider the structure of para-hydroxyacetophenone, which has a pKa value in the same range as a carboxylic acid, despite the fact that it lacks a COOH group. Offer an explanation for the acidity of para-hydroxyacetophenone. но para-Hydroxyacetopheno
> The following two compounds are constitutional isomers. Identify which of these is expected to be more acidic and explain your choice. OH H3C OH
> One of the compounds from the previous problem has a pKa < 10. Identify that compound and explain why it is so much more acidic than all of the other compounds.
> Provide an IUPAC name for each of the following compounds: он (а) (b)
> Draw the structure of each of the following compounds: a. Cyclobutanecarboxylic acid b. 3,3-Dichlorobutyric acid c. 3,3-Dimethylglutaric acid
> Provide both an IUPAC name and a common name for each of the following compounds: a. HO2C(CH2)3CO2H b. CH3(CH2)2CO2H c. C6H5CO2H d. HO2C(CH2)2CO2H e. CH3COOH f. HCO2H
> Each of the following compounds does not participate as a diene in a Diels–Alder reaction. Explain why in each case. (a) (b) (c) (d)
> After performing the reaction from Problem 16.37, the reaction flask is heated to 40ºC and two of the products become the major products. When the flask is then cooled to 0ºC, no change occurs in the product distribution. Explain why an increase in tempe
> Draw all products that are expected when 2-ethyl-3-methyl 1,3-cyclohexadiene is treated with HBr at room temperature, and show a mechanism of their formation.
> In each of the following pairs of compounds identify the compound that liberates the most heat upon hydrogenation: (a) (b)
> Treatment of 1,2-dibromocycloheptane with excess potassium tert-butoxide yields a product that absorbs UV light. Identify the product.
> Circle each compound that has a conjugated π system:
> Draw the structure of each of the following compounds: a. 1,4-Cyclohexadiene b. 1,3-Cyclohexadiene c. (Z)-1,3-Pentadiene d. (2Z,4E)-Hepta-2,4-diene e. 2,3-Dimethyl-1,3-butadiene
> Identify which of the following compounds are expected to have a pKa он H.
> For each of the following tasks, use the color wheel in Figure 16.37. a. Identify the color of a compound that absorbs orange light. b. Identify the color of a compound that absorbs blue-green light. c. Identify the color of a compound that absorbs or
