Name: hückel rule and aromatic ring criteria
Uploaded: 2023-04-30T10:31:08.000Z
Duration: 1 min 20 s
Channel: JoVE

Benzen, cyklobutadien i cyklooktatetraen są reprezentowane jako hybryda dwóch równoważnych struktur.
Jednak w przeciwieństwie do benzenu, cyklobutadien i cyklooktatetraen są niestabilne i nie są aromatyczne.
Aby wyjaśnić te różnice, Erich Hückel nakreślił zestaw cech strukturalnych leżących u podstaw aromatyczności, znanych jako reguła Hückla lub reguła 4n + 2.
Reguła Hückla mówi, że związek aromatyczny musi być cykliczny i płaski, z niehybrydyzowanym orbitalem p na każdym węglu.
Orbitale p muszą zachodzić na siebie, tworząc ciągłą pętlę (4n + 2) π elektronów, gdzie n jest dodatnią liczbą całkowitą.
Benzen spełnia wszystkie kryteria reguły Hückela, ustalając jego aromatyczność.
W przeciwieństwie do tego, cyklooktatetraen przyjmuje niepłaską konformację wanny bez nakładania się sąsiednich orbitali p. Dodatkowo brakuje mu (4n + 2) π elektronów i dlatego nie jest aromatyczny.
Podobnie cyklobutadien jest cykliczny, płaski i ma ciągłe nakładanie się orbitali p. Brakuje mu jednak (4n + 2) π elektronów i traci aromatyczność.

kryteria aromatyczności i reguła hückela 4n + 2

Criteria for Aromaticity and the H&uuml;ckel 4n + 2 Rule

Podobnie jak benzen, cyklobutadien i cyklooktatetraen są związkami cyklicznymi z naprzemiennymi wiązaniami pojedynczymi i podwójnymi. Jednak ich zachowanie chemiczne różni się od benzenu, ponieważ nie są stabilne i aromatyczne. Jakie są zatem cechy strukturalne związków nienasyconych zaliczanych do aromatycznych?

Po raz pierwszy Eric Hückel, niemiecki fizyk chemiczny, wyprowadził zestaw cech strukturalnych pozwalających sklasyfikować związek jako aromatyczny. Jest to obecnie znane jako reguła Hückela lub reguła 4n + 2. Zgodnie z tą zasadą związek aromatyczny musi być cykliczny, planarny, sprzężony w sposób ciągły, posiadający nieparzystą liczbę par elektronów π lub 4n + 2 elektronów π, gdzie n jest liczbą całkowitą (n = 0, 1, 2…). Dlatego związek aromatyczny powinien mieć 2 (n = 0), 6 (n = 1), 10 (n = 2), 14 (n = 3) itd., liczbę elektronów π lub 1, 3, 5, 7 itp., pary elektronów π.

Na przykład 1,3,5-heksatrien i benzen mają 6 elektronów π; nawet wtedy 1,3,5-heksatrien nie jest aromatyczny, ponieważ orbitale p na dwóch końcowych atomach węgla nie nakładają się, ponieważ wiązanie nie łączy tych węgli. Dlatego związki muszą być cykliczne, aby były aromatyczne.

<img alt="Figure1" src="/files/ftp_upload/12453/12453_PT-Figure_1.svg" style="text-align: center; height: 150px;">

Chociaż jest to ośmioczłonowy związek cykliczny z ciągłymi czterema wiązaniami π, cyklooktatetraen nie jest stabilny i aromatyczny. Dzieje się tak, ponieważ cyklooktatetraen nie jest płaski; przyjmuje konformację wanny. W rezultacie efektywne nakładanie się orbitali p w celu utworzenia zamkniętej pętli chmury elektronów π nie jest możliwe. Warto zauważyć, że w przeciwieństwie do benzenu ulega reakcjom addycji.

Aby związek mógł być sprzęgany w sposób ciągły, musi mieć wszystkie węgle hybrydyzacji sp^2 z w połowie wypełnionym niezhybrydyzowanym orbitalem p na każdym. Na przykład 1,3-cykloheksadien i 1,3,5-cykloheptatrien mają zhybrydyzowane atomy węgla sp^3, które nie mają niezhybrydyzowanego orbitalu p, więc ciągłe nakładanie się jest nieosiągalne. Dlatego oba nie są aromatyczne.

<img alt="Figure2" src="/files/ftp_upload/12453/12453_PT-Figure_2.svg" style="text-align: center; height: 85px;">

Z drugiej strony cyklobutadien, cykliczny, planarny związek z ciągłą koniugacją, nie jest stabilny i aromatyczny. Ma 2 pary elektronów π lub 4 elektrony π, co nie spełnia kryterium posiadania 4n + 2 elektronów π. Dlatego nie jest aromatyczny.

Kryteria aromatyczności i reguła Hückela 4n + 2

Podobnie jak benzen, cyklobutadien i cyklooktatetraen są cyklicznymi związkami z naprzemiennymi wiązaniami pojedynczymi i podwójnymi. Jednak ich zachowanie chemiczne różni się ...

criteria-for-aromaticity-and-the-hckel-4n-2-rule

Education

JoVE Core

Organic Chemistry

Chemia organiczna

Unit 1

Jednostka 1

Aromatic Compounds

Związki aromatyczne

KEY TERMS AND CONCEPTS

Kluczowe terminy i pojęcia

h&uuml;ckel rule and aromatic ring criteria

Aromatic rings follow H&amp;uuml;ckel’s rule, also called the 4n + 2 rule. This rule helps identify which unsaturated cyclic compounds are aromatic and why some ring systems are unstable instead. Benzene is the classic example, while cyclobutadiene and cyclooctatetraene show different behavior and are not aromatic.

Eric H&amp;uuml;ckel, a German chemical physicist, first described the structural features needed for aromaticity. An aromatic compound must be cyclic, planar, and continuously conjugated. It must also contain an odd number of pairs of pi electrons, which means it has 4n + 2 pi electrons, where n is an integer.

That electron pattern gives possible counts of 2, 6, 10, 14, and so on pi electrons. These are the same as 1, 3, 5, 7, and so on pairs of pi electrons. Benzene fits this pattern, and it is aromatic. Cyclobutadiene does not, even though it is cyclic and planar with continuous conjugation. It has 4 pi electrons, or 2 pairs of pi electrons, so it fails the 4n + 2 rule and is not aromatic.

A ring must also stay closed to count as aromatic. 1,3,5-Hexatriene has 6 pi electrons, like benzene, but it is not aromatic because it is not cyclic. The p orbitals on the two terminal carbon atoms do not overlap, since no bond connects those carbons.

Planarity is another key requirement. Cyclooctatetraene has four pi bonds in an eight-membered ring, but it is nonplanar and adopts a tub shape. Because of that shape, its p orbitals cannot overlap well enough to form a closed loop of pi electrons. It is unstable, not aromatic, and unlike benzene it undergoes addition reactions.

Continuous conjugation also matters. Every carbon in the ring must be sp2 hybridized and have a half-filled unhybridized p orbital. In 1,3-cyclohexadiene and 1,3,5-cycloheptatriene, some carbons are sp3 hybridized, so they do not have the needed p orbital. As a result, continuous overlap cannot happen, and both compounds are not aromatic.

H&uuml;ckel Rule and Aromatic Ring Criteria

aromatic compounds: overview

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Aromatic compounds are linked to both pleasant smells and important chemical structures. The word aromatic first came from fragrant natural sources such as fresh flowers and spices. Early organic chemists isolated benzene derivatives from oils of plants, including vanillin from vanilla, methyl salicylate from wintergreen, and cinnamaldehyde from cinnamon. The history of benzene also helped shape the idea of aromatic compounds. In 1825, Faraday isolated benzene from compressed illuminating gas,...

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Benzene derivatives with one substituent are named by attaching the substituent name to benzene. Benzene is the simplest aromatic hydrocarbon, also called an arene. For simple monosubstituted benzene compounds, IUPAC naming uses the group name as a prefix. Halogen-substituted benzene compounds follow this pattern. The halogen prefix can be fluoro, chloro, bromo, or iodo. When an alkyl group is attached to the benzene ring, the name depends on the chain length of that group. If the alkyl chain...

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Naming Benzene Rings with Multiple Groups

Naming benzene rings with multiple groups depends on how many substituents are attached. For benzene derivatives with two groups, three constitutional isomers are possible. The position of each group is described with IUPAC naming rules. For disubstituted benzene compounds, the relative positions can be shown with ortho, meta, and para. These terms are also written as o, m, and p. They can also be written with numbers, such as 1,2- for ortho, 1,3- for meta, and 1,4- for para. Dimethyl benzene,...

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Kekule’s benzene model describes benzene as a six-carbon ring with alternating pi bonds. August Kekule proposed this structure in 1865 from the formula C6H6, the idea that all benzene hydrogens are equivalent, and the rule that each carbon has four bonds because of tetravalency. In this model, each carbon is attached to one hydrogen atom. It also predicts two isomers for 1,2-disubstituted benzene derivatives. In one form, the substituted carbons are linked by a double bond, and in the other...

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Benzene π Orbitals and Electron Delocalization

Benzene has a planar ring structure with delocalized π electrons. Its six carbon atoms form a regular hexagon, and each carbon is sp2 hybridized. The C–C–C and H–C–C bond angles are 120°, which matches the flat shape of the ring. Each carbon is bonded to three other atoms. The C–H bond length is 109 pm, and the C–C bond length is 139 pm. That C–C distance is midway between the single bond length of sp3 hybridized carbons, 154 pm, and the sp2 value, 133 pm. Beneath and above the ring plane,...

criteria for aromaticity and the h&uuml;ckel 4n + 2 rule

Aromatic rings follow H&amp;uuml;ckel’s rule, also called the 4n + 2 rule. This rule helps identify which unsaturated cyclic compounds are aromatic and why some ring systems are unstable instead. Benzene is the classic example, while cyclobutadiene and cyclooctatetraene show different behavior and are not aromatic. Eric H&amp;uuml;ckel, a German chemical physicist, first described the structural features needed for aromaticity. An aromatic compound must be cyclic, planar, and continuously...

h&uuml;ckel's rule diagram of &pi; mos: frost circle

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The Frost circle is a graphical method for showing the relative energies of pi molecular orbitals in planar, fully conjugated, monocyclic compounds. It is also called the inscribed polygon method. A. A. Frost and Boris Musulin first described this method in 1953. To build a Frost circle, draw a polygon with the same number of edges as the number of carbons in the cyclic system. Place one vertex pointing downward. Then draw a circle around the polygon so that every vertex touches the circle.

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Using Frost Circles to Test Aromaticity

Frost circles help test whether a cyclic compound is aromatic by using the inscribed polygon method and Hückel’s 4n + 2 rule. A compound is stable and aromatic when every bonding molecular orbital (MO) is completely filled with a pair of electrons. If electrons occupy non-bonding or antibonding orbitals, the compound is unstable and not aromatic. Frost circle diagrams for cycloalkenes with 4 to 8 carbons show a clear pattern. The number of bonding MOs is always odd. The electrons needed to...

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Cyclopentadienyl Anion and Aromaticity

Cyclopentadiene is a neutral hydrocarbon that is not aromatic. It contains an odd number of carbon atoms and one CH2 group in the ring. With only 4 pi electrons, it does not follow the 4n + 2 pi electron rule. The CH2 carbon is sp3 hybridized, so it has no vacant p orbital to keep p orbitals overlapped around the ring. That break in overlap stops pi electrons from spreading across the entire ring. As a result, cyclopentadiene does not meet the usual aromaticity criteria. If one hydrogen is...

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Cycloheptatrienyl Cation and Aromaticity

Cycloheptatriene is a neutral monocyclic unsaturated hydrocarbon with seven carbon atoms. One carbon in the ring is sp3 hybridized, which breaks the continuous overlap of p orbitals. Even though the ring has three double bonds and 6 π electrons, cycloheptatriene is not aromatic because the p orbitals do not form one uninterrupted loop. Removing one hydrogen from the CH2 group changes the ring. If that hydrogen is removed with both, one, or no electrons, the products are the cycloheptatrienyl...

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Five-Membered Aromatic Rings with Heteroatoms

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Aromatic Ring Shifts in NMR Spectra

Aromatic ring shifts in NMR spectra help identify aromatic compounds using proton NMR and carbon-13 NMR. Aromatic hydrogens are often strongly deshielded by the aromatic ring current, so they usually appear in the 6.5–8.0 ppm range in proton NMR. In benzene, the hydrogens directly bonded to the ring absorb at 7.3 ppm. Larger aromatic rings can place hydrogens outside the usual range. In [18]annulene, the 12 outer hydrogens are highly deshielded by the ring current and absorb downfield at 9.3...

key terms and concepts

Learn the H&uuml;ckel 4n + 2 rule and the key features of aromatic rings, including cyclic shape, planarity, continuous conjugation, and pi electrons.

H&uuml;ckel Rule and Aromatic Ring Criteria | JoVE K12

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Hückel Rule and Aromatic Ring Criteria

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