Ethanol is the alcohol contained in alcoholic beverages. CHAPTER 8 Hydroxy Functional Group: Alcohols Properties,Preparation,and 公兰会 Strategy of Synthesis 8-1 Naming the Alcohols dature of alcohols treats them as OH 1-Propandd .5.Triaeth -3-a 8oagareleohakanetandteabonann HO CHCH, 1-Ets Nlcohols can be classified as primary,secondary or tertiary a.sheb28sGo6tes5setooer o860s6a RCH.OH The bond than that o时the 104 kcal 1
1 CHAPTER 8 Hydroxy Functional Group: Alcohols Properties, Preparation, and Strategy of Synthesis Ethanol is the alcohol contained in alcoholic beverages. Yeast enzymes C H O 2 CH CH OH + 2 CO 6 12 6 3 2 2 ⎯⎯⎯⎯⎯→ Alcohols can be thought of as a derivative of water in which a hydrogen atom has been replaced by an alkyl group. Replacement of the 2nd hydrogen on the water molecule leads to an ether. 8-1 Naming the Alcohols The systematic nomenclature of alcohols treats them as derivatives of alkanes. The –e is dropped from the alkane name and is replaced by –ol. Alkane Æ Alkanol In complicated, branched alkanes, the name of the alcohol is based on the longest chain containing the –OH group. Other substituents are then named using the IUPAC rules for hydrocarbons. The number of the chain is from the end closest to the OH group. Cyclic alcohols are called cycloalkanols and the carbon carrying the –OH group is the 1 carbon. Alcohols can be classified as primary, secondary or tertiary: In common notation (non-IUPAC), the word alcohol directly follows the name of the alkane. •Methyl alcohol •Isopropyl alcohol •Tert-Butyl alcohol 8-2 Structural and Physical Properties of Alcohols The structure of alcohols resembles that of water. In the structures of water, methanol, and methoxymethane, the oxygen atoms are all sp3+ hybridized and their bond angles are all nearly tetrahedral. The O-H bond is shorter than the C-H bonds. The bond strength of the O-H bond is greater than that of the C-H bonds: •DHo O-H = 104 kcal mol-1 •DHo C-H = 98 kcal mol-1
ohet0H83aydarencebetwenomygenand Hgdee8nubandeaoiesnhe.boingpointsand orap5hggm522hieentcomparedtothe and hal DHte ~5-6 kcal mol .Covalent O-H DH 104 kcal mol other en吗Tot 88 neettangfnkcaheaersoub Aohols are pua proticsovor B3anoaiconan6neshatofwater The acidity constant for an alcohol can be defined as: Re+R+HO n8e股8e5。 aw←a0 The ea CHCHo f+Na-OH CHCHONa'+HO 2
2 Due to the electronegativity difference between oxygen and hydrogen, the O-H bond is polar. Hydrogen bonding raises the boiling points and water solubilities of alcohols. Alcohols have unusually high boiling points compared to the corresponding alkanes and haloalkanes. Hydrogen bonding between alcohol molecules is much stronger than the London forces and dipole-dipole interactions in alkanes and haloalkanes, although much weaker than O-H covalent bonds. •O···H-O DHo ~ 5-6 kcal mol-1 •Covalent O-H DHo = 104 kcal mol-1. The extensive network of H-bonds between neighboring alcohol molecules makes it difficult for a molecule to leave the surface of the liquid. An alcohol molecule makes slightly less than 2 hydrogen bonds to other alcohol molecules on the average. A water molecule, on the other hand, forms hydrogen bonds to slightly less than 4 other water molecules. Water has an abnormally high boiling point for a molecule of its size due to this hydrogen bonding. Many alcohols are appreciably soluble in water whereas their parent alkanes are not. •Alkanes and most alkyl chains are said to be hydrophobic (water-hating). In order to dissolve, alkanes must interrupt the strong hydrogen bonding between water molecules which is then replaced by weaker dipole-induced dipole forces (ΔH > 0). In addition, long hydrocarbon chains force water molecules to form a cage-like (or clathrate) structure about the nonpolar chain which greatly reduces the entropy of the water molecules involved (ΔS < 0). The –OH groups of alcohols (as well as groups like –COOH and –NH2) are said to be hydrophilic (water-loving) and enhance solubility. The longer the alkyl chain of an alcohol, the lower its solubility in water (it looks more and more like an alkane). Alcohols are popular protic solvents for SN2 reactions. 8-3 Alcohols as Acids and Bases The acidity of alcohols resembles that of water. The acidity constant for an alcohol can be defined as: + - 3 -1 a2 a [H O ][RO ] K = K[H O] = mol L , and pKa = -log K [ROH] Alcohols are acidic compared to alkanes and haloalkanes because the electronegative oxygen atom is able to stabilize the negative charge of the alkoxide ion. To drive the alcohol/alkoxide equilibrium towards the conjugate base, a base stronger than alkoxide must be used to remove the proton: The equilibrium constant for this reaction is about 1019.5. Alkoxides in less that stoichiometric equilibrium concentrations can be generated by adding a metal hydroxide to an alcohol: At equimolar starting concentrations, about ½ of the alcohol is converted to alkoxide. If the alcohol is the solvent, all of the base is in the alkoxide form (Le Châtelier’s principle)
inducive che giore8grbaieasntheaenolncresstheaanyol The lone electron pairs on oxygen make alcohols ndcCono and maanm5c8aayyn C0+25 Ceo0.25oC9010马CH,OH A change of catalyst leads to the production of 1,2-ethanedio 羽 2C0+3H,, CH一CH sgotoaaanoe Synthesis gas itself can be prepared from coal: CmaxC0+y Synthesis of Alcohols by Nucleophilic Substitution CH-CH HOH 父 3
3 Steric disruption and inductive effects control the acidity of alcohols. The acidity of an alcohol varies (relative pKa in solution): Strongest acid Weakest acid CH3OH < primary < secondary < tertiary This ordering is due to solvation and hydrogen bonding in the more sterically hindered alcohols. The presence of halogens in the alcohol increases the acidity of the alcohol due to an inductive effect. The electronegative halogen atom polarizes the X-C bond producing a partial positive charge on the carbon atom. This charge is further transmitted through the C-O σ bond to the oxygen atom which is then better able to stabilize the negative charge on the alkoxide oxygen. Inductive effects increase with the number of electronegative groups and decreases with the distance from the oxygen. The lone electron pairs on oxygen make alcohols basic. Alcohols may be weakly basic as well as being acidic. Molecules that can be both acidic and basic are called amphoteric. Very strong acids are required to protonate alcohols. Industrial Sources of Alcohols: Carbon Monoxide and Ethene 8-4 Methanol is commercially synthesized from synthesis gas, a mixture of CO and H2: A change of catalyst leads to the production of 1,2-ethanediol: Synthesis gas itself can be prepared from coal: Ethanol can be prepared by the fermentation of sugars or the hydration of ethene: 8-5 Synthesis of Alcohols by Nucleophilic Substitution If the required halides are available, the corresponding alcohols can be prepared by SN2 and SN1 processes using hydroxide and water respectively as nucleophiles. These methods have some drawbacks: •Bimolecular elimination is possible in hindered systems •Tertiary halides form carbocations which may undergo E1 reactions. The use of polar, aprotic solvents alleviates some of these problems
8-6 Step1:Acetate formation (S2 reaction) have special meanings in StepCo(hydo) -0R -8e-i-: tmlaenaeantedpyanudophicndr Be代acamtgcsC:ceertanatehedioeon,an 4
4 The problem of elimination in SN2 reactions of oxygen nucleophiles with secondary or sterically encumbered, branched primary substrates is the use of acetate as a less basic nucleophile. Step 1: Acetate formation (SN2 reaction) Step 2: Conversion to alcohol (hydrolysis) Synthesis of Alcohols: Oxidation-Reduction Relation between Alcohols and Carbonyl Compounds 8-6 Oxidation and reduction have special meanings in organic chemistry. A process that adds electronegative atoms such as halogen or oxygen to a molecule constitutes an oxidation. A process that removes hydrogen from a molecule also constitutes an oxidation. The reversal of either of these two steps constitutes a reduction. Step-by-Step Oxidation of CH4 to CO2: Aldehydes and primary alcohols, ketones and secondary alcohols can be interconverted using reduction and oxidation reactions involving 2 atoms of hydrogen: Reduction of carbonyl compounds is carried out using hydride reagents. Alcohols can form by hydride reduction of the carbonyl group The carbonyl functional group is polarized due to the high electronegativity of the carbonyl oxygen atom: The carbonyl carbon can be attacked by a nucleophilic hydride ion, H- , furnished by a hydride reagent. Sodium borohydride, NaBH4, and lithium aluminum hydride, LiAlH4, are commonly used for hydride reductions because their solubilities are higher in common organic solvents than LiH and NaH. These reductions are achieved by the addition of a H- ion to the electropositive carbon and a proton to the electronegative oxygen. The reactivity of NaBH4 is much lower than a free hydride ion, and NaBH4 can be used in protic solvents such as ethanol. The mechanism of a sodium borohydride reduction involves: •Donation of H- to the carbonyl carbon •Simultaneous protonation of the carbonyl oxygen by a solvent molecule •Combination of the boron fragment with the ethoxide ion to yield sodium ethoxyborohydride The resulting sodium ethoxyborohydride is capable of another three reductions, thus four equivalents of aldehyde or ketone can be reduced to alcohol
dcbereverd &oosnRe.8gedekoaehydsandketonsusn iIl。+4H,OH feoerbtgaibn2t ne the ie2taeoergonaomrocdaetoartoyccswh 5c2eaoc3aesnoh Ovo 空 B7ogaeamon6Reatgamasowuceoph natomctaprmoenandaHc0:lon w-OH+ mer()d nto Cr()and Cr(V). me Cr(V)may. 5
5 The reactivity of LiAlH4 is much greater than that of NaBH4 and is less selective in its reactions. LiAlH4 reacts vigorously with water and ethanol and must be used in an aprotic solvent such as diethyl ether. All four hydrogens in a LiAlH4 molecule are available for reductions, thus lithium aluminum hydride can reduce four aldehyde or ketone molecules to alcohols. After the reaction is carried out, aqueous acid is added to consume the excess reagent and release the product alcohol from the tetraalkoxyaluminate. Alcohol synthesis by reduction can be reversed: chromium reagents. Alcohols can be oxidized back to aldehydes and ketones using chromium (VI) compounds. During this process, the yellow-orange Cr(VI) species is reduced to a deep green Cr(III) species. K2Cr2O7 or Na2Cr2O7, or CrO3 are commonly used Cr(VI) reagents. Secondary alcohols can be oxidized to ketones in aqueous solution: Primary alcohols tend to overoxidize to carboxylic acids when oxidized in aqueous solution: Overoxidation of primary alcohols is not a problem in the absence of water. The oxidizing agent, pyridinium chlorochromate (pyH+CrO3Cl- ) can be used in dichloromethane to successfully oxidize these alcohols: PCC oxidation is also used with secondary alcohols instead of the aqueous chromate method to minimize side reactions and improve yields. Tertiary alcohols cannot be oxidized by chromium reagents since the alcoholic carbon atom carries no hydrogen atoms and cannot readily form a double bond with the oxygen. Chromic esters are intermediates in alcohol oxidation. The mechanism of chromium(VI) oxidations involves two steps: •Formation of a chromic ester •E2 elimination of a proton and a HCrO3 - ion. The Cr(IV) species disproportionates into Cr(III) and Cr(V). The Cr(V) may also function as an oxidizing agent. Organometallic Reagents: Sources of Nucleophilic Carbon for Alcohol Synthesis 8-7 If the carbonyl carbon of an aldehyde or ketone could be attacked by a nucleophilic carbon atom, R:- , instead of a hydride ion, both an alcohol and a new carbon-carbon bond would be formed. The class of compounds called organometallic reagents are strong bases and good nucleophiles and are useful in this kind of synthesis