23Mar 2014 by Vincent Summers No Comments

The Quintessential Aromatic Hydrocarbon Benzene (Pt.2)

Chemistry
[caption id="attachment_6069" align="alignright" width="440"] Benzene De-localized Pi-system - CCA Share Alike 3.0 Unported by Vladsinger[/caption] In Part One of The Quintessential Aromatic Hydrocarbon Benzene, we saw that the so-called 1,3,5-cyclohexatriene was really not completely described by the structure that that name implies. It is equivalent to 2,4,6-cyclohexatriene (if you flip the 1,3,5- structure over, and you get the 2,4,6- structure), and includes a variety of other contributing factors. Although we did not list them, they may include ionic contributors.1 In general, these are discounted. Visualizing Benzene's Structure The conclusion is that the compound actually has six equivalent bonds between adjacent carbon atoms, forming six internal angles angle each equal to 60°. The bonds are each, then, “single-and-one-half” bonds between each carbon pair. The molecule is flat, even as a collection…
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23Mar 2014 by Vincent Summers No Comments

The Quintessential Aromatic Hydrocarbon Benzene (Pt.1)

Chemistry
[caption id="attachment_14959" align="alignright" width="440"] Cyclohexane - Chair Form[/caption] Benzene? What's that? Living creatures universally share an important characteristic: they all are constructed of carbon-containing compounds. For that reason, chemists call such compounds organic. Now the term organic has taken on additional meaning. Compounds that are similar, but not found in nature, are also called organic compounds. One group of organic compounds, whether found in nature or not, possess special properties—chemical and physical—that put them into a category apart. Once it was thought such compounds were distinguishable by smell or aroma. Each was labeled an aromatic, and—the property itself—aromaticity. Simple Hydrocarbons The simplest hydrocarbon1 is methane (CH4)—a gas. It possesses a tetrahedral structure, with a carbon atom at its center and four hydrogen atoms at the corners (See Figure 1). Since…
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21Mar 2014 by Vincent Summers 2 Comments

The Aromatic Cyclopentadienyl Anion

Chemistry, Education
[caption id="attachment_16480" align="alignright" width="440"] Cyclopentadienyl Anion[/caption] Is it possible that for an ion to be aromatic? Yes. Consider the aromatic cyclopentadienyl anion. Hückel’s Rule dictates a flat ring with 4n + 2 π (pi) conjugated electrons. The smallest neutral ring with these qualifications has n = 1. It is benzene (C₆H₆). But Hückel’s law does not require an electronically neutral structure. The smallest aromatic ion is the cyclopropenyl cation¹ (C₃H₃⁺). Is there a negative ion that has 6 π electrons and is aromatic? The answer is yes. The aromatic cyclopentadienyl anion (C₅H₅⁻). Neutral Cyclopentadiene Neutral cyclopentadiene is flat. It is pentagon shaped. Three of the carbon-carbon bonds are single bonds. The other two are double bonds. At each of the four ends of the two double bonds there is one…
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14Dec 2012 by Vincent Summers No Comments

Aromatic Tropylium Ion

Chemistry
[caption id="attachment_20212" align="alignright" width="440"] Aromatic tropylium cation[/caption] Aromatics are separate category of organic compounds. Often aromatic compounds are electrically neutral. However, a few do carry a charge. They are ions.¹ In fact many aromatic ions would not be aromatic if they lost their charge. We will consider the aromatic tropylium cation in this article. Three Carbon Atoms The smallest aromatic ion is the cyclopropenyl cation. The neutral cyclopropene molecule possesses 4 π-electrons. That is not an aromatic number. By making it a cation, it loses 2 of them, meeting the qualification for aromatic compounds.¹ [caption id="attachment_16191" align="alignright" width="240"] Spacefill Model.[/caption] Four Carbon Atoms On the basis of π-electron count alone, one might suppose a cyclobutadienyl di-anion or a cyclobutadienyl di-cation, would display aromaticity. That is not the case. There are…
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