1. John E. McMurry http://www.cengage.com/chemistry/mcmurry Paul D. Adams University of Arkansas Chapter 17 Alcohols and Phenols

2.  Alcohols contain an OH group connected to a saturated C (sp 3 )  They are important solvents and synthesis intermediates  Phenols contain an OH group connected to a carbon in a benzene ring  Methanol, CH 3 OH, called methyl alcohol, is a common solvent, a fuel additive, produced in large quantities  Ethanol, CH 3 CH 2 OH, called ethyl alcohol, is a solvent, fuel, beverage  Phenol, C 6 H 5 OH (“phenyl alcohol”) has diverse uses - it gives its name to the general class of compounds  OH groups bonded to vinylic sp 2 -hybridized carbons are called enols Alcohols and Phenols

3.  To begin to study oxygen-containing functional groups  These groups lie at the heart of biological chemistry Why this Chapter?

4.  General classifications of alcohols based on substitution on C to which OH is attached  Methyl (C has 3 H’s), Primary (1°) (C has two H’s, one R), secondary (2°) (C has one H, two R’s), tertiary (3°) (C has no H, 3 R’s) 17.1 Naming Alcohols and Phenols

5.  Select the longest carbon chain containing the hydroxyl group, and derive the parent name by replacing the -e ending of the corresponding alkane with -ol  Number the chain from the end nearer the hydroxyl group  Number substituents according to position on chain, listing the substituents in alphabetical order IUPAC Rules for Naming Alcohols

6.  Use “phenol” (the French name for benzene) as the parent hydrocarbon name, not benzene  Name substituents on aromatic ring by their position from OH Naming Phenols

7.  The structure around O of the alcohol or phenol is similar to that in water, sp 3 hybridized.  Alcohols and phenols have much higher boiling points than similar alkanes and alkyl halides.  A positively polarized  OH hydrogen atom from one molecule is attracted to a lone pair of electrons on a negatively polarized oxygen atom of another molecule.  This produces a force that holds the two molecules together  These intermolecular attractions are present in solution but not in the gas phase, thus elevating the boiling point of the solution. 17.2 Properties of Alcohols and Phenols

8.  Weakly basic and weakly acidic  Alcohols are weak Brønsted bases  Protonated by strong acids to yield oxonium ions, ROH 2 + Properties of Alcohols and Phenols: Acidity and Basicity

9.  Can transfer a proton to water to a very small extent  Produces H 3 O + and an alkoxide ion, RO , or a phenoxide ion, ArO  Alcohols and Phenols are Weak Brønsted Acids

10.  The acidity constant, K a, measures the extent to which a Brønsted acid transfers a proton to water [A  ] [H 3 O + ] K a = —————and pK a =  log K a [HA]  Relative acidities are more conveniently presented on a logarithmic scale, pK a, which is directly proportional to the free energy of the equilibrium  Differences in pK a correspond to differences in free energy  Table 17.1 presents a range of acids and their pK a values Acidity Measurements

11. pK a Values for Typical OH Compounds

12.  Simple alcohols are about as acidic as water  Alkyl groups make an alcohol a weaker acid  The more easily the alkoxide ion is solvated by water the more its formation is energetically favored  Steric effects are important Relative Acidities of Alcohols

13.  Electron-withdrawing groups make an alcohol a stronger acid by stabilizing the conjugate base (alkoxide) Inductive Effects Also Important in Determining Acidity of Alcohols

14.  Alcohols are weak acids – requires a strong base to form an alkoxide such as NaH, sodium amide NaNH 2, and Grignard reagents (RMgX)  Alkoxides are bases used as reagents in organic chemistry Generating Alkoxides from Alcohols

15.  Phenols (pK a ~10) are much more acidic than alcohols (pK a ~ 16) because of resonance stabilization of the phenoxide ion  Phenols react with NaOH solutions (but alcohols do not), forming salts that are soluble in dilute aqueous solution  A phenolic component can be separated from an organic solution by extraction into basic aqueous solution and is isolated after acid is added to the solution Phenol Acidity

16.  Phenols with nitro groups at the ortho and para positions are much stronger acids Nitro-Phenols

17.  Alcohols are derived from many types of compounds  The alcohol hydroxyl can be converted to many other functional groups  This makes alcohols useful in synthesis 17.3 Preparation of Alcohols: A Review

18.  Hydroboration/oxidation: syn, anti-Markovnikov hydration  Oxymercuration/reduction: Markovnikov hydration Review: Preparation of Alcohols by Regiospecific Hydration of Alkenes

19.  Review: Cis-1,2-diols from hydroxylation of an alkene with OsO 4 followed by reduction with NaHSO 3  Trans-1,2-diols from acid-catalyzed hydrolysis of epoxides 1,2-Diols

20. What is the major product?

21.  Reduction of a carbonyl compound in general gives an alcohol  Note that organic reduction reactions add the equivalent of H 2 to a molecule 17.4 Alcohols from Carbonyl Compounds: Reduction

22.  Aldehydes gives primary alcohols  Ketones gives secondary alcohols Reduction of Aldehydes and Ketones

23.  NaBH 4 is not sensitive to moisture and it does not reduce other common functional groups  Lithium aluminum hydride (LiAlH 4 ) is more powerful, less specific, and very reactive with water  Both add the equivalent of “H - ” Reduction Reagent: Sodium Borohydride

24.  The reagent adds the equivalent of hydride to the carbon of C=O and polarizes the group as well Mechanism of Reduction

25.  Carboxylic acids and esters are reduced to give primary alcohols  LiAlH 4 is used because NaBH 4 is not effective Reduction of Carboxylic Acids and Esters

26. From carboxylic acids and esters

27. summary

28. What is the reagent

29.  Alkyl, aryl, and vinylic halides react with magnesium in ether or tetrahydrofuran to generate Grignard reagents, RMgX  Grignard reagents react with carbonyl compounds to yield alcohols 17.5 Alcohols from Carbonyl Compounds: Grignard Reagents

30. Reactions of Grignard Reagents with Carbonyl Compounds

31.  Yields tertiary alcohols in which two of the carbon substituents come from the Grignard reagent  Grignard reagents do not add to carboxylic acids – they undergo an acid-base reaction, generating the hydrocarbon of the Grignard reagent Reactions of Esters and Grignard Reagents

32.  Cannot be prepared if there are reactive functional groups in the same molecule, including proton donors Grignard Reagents and Other Functional Groups in the Same Molecule

33.  Grignard reagents act as nucleophilic carbon anions (carbanions = : R  ) in adding to a carbonyl group  The intermediate alkoxide is then protonated to produce the alcohol Mechanism of the Addition of a Grignard Reagent

35.  Conversion of alcohols into alkyl halides: - 3˚ alcohols react with HCl or HBr by S N 1 through carbocation intermediate - 1˚ and 2˚ alcohols converted into halides by treatment with SOCl 2 or PBr 3 via S N 2 mechanism 17.6 Reactions of Alcohols

36. Reactions of 1˚ and 2˚ alcohols

37.  Reaction with p-toluenesulfonyl chloride (tosyl chloride, p- TosCl) in pyridine yields alkyl tosylates, ROTos  Formation of the tosylate does not involve the C–O bond so configuration at a chirality center is maintained  Alkyl tosylates react like alkyl halides Conversion of Alcohols into Tosylates

38.  The S N 2 reaction of an alcohol via an alkyl halide proceeds with two inversions, giving product with same arrangement as starting alcohol  The S N 2 reaction of an alcohol via a tosylate, produces inversion at the chirality center Stereochemical Uses of Tosylates

39.  The general reaction: forming an alkene from an alcohol through loss of O-H and H (hence dehydration) of the neighboring C–H to give  bond  Specific reagents are needed Dehydration of Alcohols to Yield Alkenes

40.  Tertiary alcohols are readily dehydrated with acid  Secondary alcohols require severe conditions (75% H 2 SO 4, 100°C) - sensitive molecules do not survive  Primary alcohols require very harsh conditions – impractical  Reactivity is the result of the nature of the carbocation intermediate Acid- Catalyzed Dehydration

43.  Phosphorus oxychloride in the amine solvent pyridine can lead to dehydration of secondary and tertiary alcohols at low temperatures  An E2 reaction via an intermediate ester of POCl 2 (see Figure 17.7) Dehydration with POCl 3

44. Incorporation of Alcohols into Esters

45.  Can be accomplished by inorganic reagents, such as KMnO 4, CrO 3, and Na 2 Cr 2 O 7 or by more selective, expensive reagents 17.7 Oxidation of Alcohols

46.  To aldehyde: pyridinium chlorochromate (PCC, C 5 H 6 NCrO 3 Cl) in dichloromethane  Other reagents produce carboxylic acids Oxidation of Primary Alcohols

47.  Effective with inexpensive reagents such as Na 2 Cr 2 O 7 in acetic acid  PCC is used for sensitive alcohols at lower temperatures Oxidation of Secondary Alcohols

48.  Alcohol forms a chromate ester followed by elimination with electron transfer to give ketone  The mechanism was determined by observing the effects of isotopes on rates Mechanism of Chromic Acid Oxidation

49.  Hydroxyl groups can easily transfer their proton to a basic reagent  This can prevent desired reactions  Converting the hydroxyl to a (removable) functional group without an acidic proton protects the alcohol 17.8 Protection of Alcohols

50.  Reaction with chlorotrimethylsilane in the presence of base yields an unreactive trimethylsilyl (TMS) ether  The ether can be cleaved with acid or with fluoride ion to regenerate the alcohol Methods to Protect Alcohols

52.  An example of TMS-alcohol protection in a synthesis Protection-Deprotection

53.  Industrial process from readily available cumene  Forms cumene hydroperoxide with oxygen at high temperature  Converted into phenol and acetone by acid 17.9 Phenols and Their Uses

54. Mechanism of Formation of Phenol

55.  The hydroxyl group is a strongly activating, making phenols substrates for electrophilic halogenation, nitration, sulfonation, and Friedel–Crafts reactions  Reaction of a phenol with strong oxidizing agents yields a quinone  Fremy's salt [(KSO 3 ) 2 NO] works under mild conditions through a radical mechanism 17.10 Reactions of Phenols

56.  Ubiquinones mediate electron-transfer processes involved in energy production through their redox reactions Quinones in Nature

57.  Characteristic O–H stretching absorption at 3300 to 3600 cm  1 in the infrared  Sharp absorption near 3600 cm -1 except if H-bonded: then broad absorption 3300 to 3400 cm  1 range  Strong C–O stretching absorption near 1050 cm  1 (See Figure 17.11)  Phenol OH absorbs near 3500 cm -1 17.11 Spectroscopy of Alcohols and Phenols

58.  13 C NMR: C bonded to  OH absorbs at a lower field,  50 to 80  1 H NMR: electron-withdrawing effect of the nearby oxygen, absorbs at  3.5 to 4 (See Figure 17-13)  Usually no spin-spin coupling between O–H proton and neighboring protons on C because of exchange reactions with moisture or acids  Spin–spin splitting is observed between protons on the oxygen-bearing carbon and other neighbors  Phenol O–H protons absorb at  3 to 8 Nuclear Magnetic Resonance Spectroscopy

59.  Alcohols undergo alpha cleavage, a C–C bond nearest the hydroxyl group is broken, yielding a neutral radical plus a charged oxygen-containing fragment  Radical cation alcohols undergo dehydration to yield an alkene radical anion Mass Spectrometry

60. Predict the product from reaction of the following substance with NaBH 4 ; then H 3 O +. Let’s Work a Problem

61. Answer There is no product formed with this series of reagents because NaBH 4 reduces esters very slowly and does not reduce carboxylic acids at all.