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EXISTING SUBSTITUENTS DIRECT THE POSITION OF ELECTROPHILIC AROMATIC SUBSTITUTION An existing group on a benzene ring can direct the position of a new group added by an electrophilic aromatic substitution (EAS) reaction. Ortho-para directors predominantly direct the incoming group to an ortho or para position. (FIGURE CANNOT COPY) G is an ortho-para director. Ortho product Para product Meta directors predominantly direct the incoming group to a meta position. (FIGURE CANNOT COPY) G is a meta director. Meta product These directing effects stem the initial substituent's electron-donating or electron withdrawing properties. Electron-donating and electron-withdrawing effects are caused by resonance, induction, or both. Of these two, when both effects are possible, resonance plays a greater role than induction. As we shall also see, electron-donating groups activate (enhance) the reactivity of a ring toward EAS, and electron-withdrawing groups deactivate (reduce) EAS reactivity. A Ortho-Para Directors The unshared electron pair of an existing ring substituent causes electrophilic aromatic substitution to take place at the ortho and para positions. Para substitution usually predominates over ortho due to steric effects. For example, acetanilide undergoes nitration primarily at the para position, with only a trace of the ortho product formed. (FIGURE CANNOT COPY) Acetanilide $p$ -Nitroacetanilide $(90 \%)$ o-Nitroacetanilide (trace) Strongly activating groups can cause substitution at both the ortho and para positions. For example, aniline and phenol both react with bromine to produce products that are fully substituted at their ortho and para positions. Amino and hydroxyl substituents are strong activating groups. (FIGURE CANNOT COPY) 2,4,6 -Tribromoaniline $(-100 \%)$ $2,4,6-$ Tribromophenol $(-100 \%)$ We can account for the predominance of ortho and para versus meta substitution, as well as the greater reactivity of aniline and phenol relative to acetanilide, by considering resonance structures for the arenium ions that would result from attack on aniline by a generic electrophile $\mathrm{E}^{+}$ at the ortho, meta, and para positions, as shown here. Ortho Attack (FIGURE CANNOT COPY) Meta Attack (FIGURE CANNOT COPY) Para Attack (FIGURE CANNOT COPY) Relatively stable contributor As we see here, four reasonable resonance structures can be written for the arenium ions resulting from ortho and para attack, whereas only three can be written for the arenium ion that results from meta attack. This observation, in itself, suggests that the ortho-and para-substituted arcnium ions should be more stable. Of greater importance, however, are the relatively stable structures that contribute to the hybrid for the ortho- and para-substituted arenium ions. In these structures, nonbonding pairs of clectrons from nitrogen form an additional covalent bond to the carbon of the ring. This extra bond-and the fact that every atom in each of these structures has a complete outer octet of electrons makes these structures the most stable of all of the contributors. Because these structures are unusually stable, they make a large - and stabilizing - contribution to the hybrid. This means, of course, that the ortho- and para-substituted arenium ions themselves are considerably more stable than the arenium ion that results from the meta attack. As a result, electrophiles react at the ortho and para positions very rapidly. Use resonance theory to explain why the hydroxyl group of phenol is an activating group and an ortho-para director. Illustrate your explanation by showing the arenium ions formed when phenol reacts with a Br' ion at the ortho, meta, and para positions. We can account for the lower reactivity of acctanilide relative to aniline and phenol on the basis of resonance involving the carbonyl group in acctanilide. In acctanilide the unshared electron pair on the nitrogen can be delocalized into the carbonyl of the amide functional group, thus diminishing availability of the electron pair for contribution to the resonance structures of the arenium ion. In aniline or phenol, this resonance effect is not possible due to absence of the carbonyl group. Thus, the amide group of acctanilide is less activating than the amino group of aniline or the hydroxyl group of phenol. (FIGURE CANNOT COPY) Electron donation to the ring by resonance is reduced when there is an alternative resonance pathway away from the ring. Phenol reacts with acetic anhydride in the presence of sodium acetate to produce the ester phenyl acetate: (FIGURE CANNOT COPY) Phenol Phenyl acetate The $-\mathrm{OCOCH}_{3}$ group of phenyl acetate, like the $-\mathrm{OH}$ group of phenol (Practice Problem 15.6 ), is an ortho-para director. (a) What structural feature of the $-$ OCOCH $_{3}$ group explains this? (b) Phenyl acetate, although undergoing reaction at the ortho and para positions, is less reactive toward electrophilic aromatic substitution than phenol. Use resonance theory to explain why this is so. Halogen atoms are also ortho-para directors by resonance, but they deactivate the ring toward electrophilic aromatic substitution by their electronegativity. Their unshared clectron pairs stabilize the arenium ion by resonance, but this stabilization is limited by the mismatch in atomic size and orbital overlap between carbon and the halogens (except for fluorine), versus the more effective resonance orbital overlap between carbon and oxygen or nitrogen. Thus, halogens are deactivating because their electronegativity destabilizes the arenium ion, yet they are ortho-para directors as a result of resonance. Alkyl groups are ortho-para directors, as well. Alkyl groups stabilize the arenium ion through inductive release of electrons, similar to the way an ordinary carbocation (e.g., a carbocation that is not conjugated like an arenium ion) is stabilized by adjacent alkyl groups. We find, for example, that when toluene undergoes electrophilic substitution, most of the substitution takes place at its ortho and para positions. When we nitrate toluene with nitric and sulfuric acids, we get mononitrotoluenes in the following relative proportions:
(FIGURE CANNOT COPY) o-Nitrotoluene $(59 \%)$ $p$ -Nitrotoluene $(37 \%)$ $m$ -Nitrotoluene $(4 \%)$ Of the mononitrotoluenes obtained from the reaction, $96 \%$ ( $59 \%+37 \%$ ) have the nitro group in an ortho or para position. Only $4 \%$ have the nitro group in a meta position. Predominant substitution of toluene at the ortho and para positions is not restricted to nitration reactions. The same behavior is observed in halogenation, sulfonation, and so forth. To understand the predominance of ortho and para substitution in toluene, let's consider the arenium ions that would result from attack on toluene by a generic electrophile $\mathrm{E}^{+}$ at the ortho, meta, and para positions. The trifluoromethyl group is a meta dircctor. Explain why this is so using resonance structures for the arenium ions that would result upon ortho, meta, and para bromination of trifluoromethylbenzene. (TABLE CANNOT COPY) Label each of the following aromatic rings as activated or deactivated based on the substituent attached, and state whether the group is an ortho-para or meta director. (FIGURE CANNOT COPY) STRATEGY AND ANSWER: If a substituent donates electron density it will activate the ring and cause ortho and para substitution. If a substituent withdraws electron density it will deactivate the ring and cause meta substitution (except for halogens, which are electron withdrawing but cause ortho-para substitution). (a) Activated; an ether is an ortho-para dircctor; (b) deactivated; the ester carbonyl is a meta dircctor; (c) activated; the single-bonded oxygen of the ester is directly bonded to the ring, and therefore it is an ortho-para dircctor; (d) activated; the amide nitrogen is an ortho-para director; (e) deactivated; however, the halogen is ortho-para director through resonance; (f) deactivated; the sulfonate group is a meta director. Predict the major products formed for each of the following. If the major products would be a mixture of ortho and para isomers, you should so state. (a) Toluene is sulfonated. (c) Nitrobenzene is brominated. (b) Benzoic acid is nitrated. (d) Isopropylbenzene reacts with acetyl chloride and AlCl_s.

Fennel visited, which can be produced from funeral, is less reactive than funeral in automatic. There are a few exceptions fearful. Explain what it's this, but the group is still Order Pereira director. Just like hydroxy group, you know, So I don't see a group in. Fino is a force of credit director because over too long in the pants, which supplies elections, most it through the orphan and better positions, this group still has to look natural in prayer on oxygen, which pretty X the same way as the age group. In funeral, however, the compound is less reactive because for conjugation off long and compare with adjusting Gruber. No, which most away park the church former our since one So the little there compares on oxygen become less active.

Explain why the connection without good excites and we've been excited. It's two different products. Let's look at the mechanism with our without backsides but the Nation actress first step and it produces Benzie like Come Pick a Time which is further stabilized by untraditional. Were fifteens in it in, for instance. Oh, structure was shows conjugation and this camera car time is most stable with public art time at this common, which is making conjugation with the benzene in. That's why this the assured direction off the reaction and a combination with BR minus gives you the major product in the prisons or both sides they have taken. Spacious is different. That's the radical of woman and unethical of woman. Also wants toe form Benzia political fishhook, and it's, ah, most able than medical at this carbon. For the same reason that would be liking education off the benzene green. And then on the next step over chain propagation, the medical reacts with them. HBR Junior is another. They are dark and gives the product


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