Archive for the ‘reaction mechanism’ Category

Enantioselective epoxidation of alkenes using the Shi Fructose-based catalyst. An undergraduate experiment.

Tuesday, April 15th, 2014

The journal of chemical education can be a fertile source of ideas for undergraduate student experiments. Take this procedure for asymmetric epoxidation of an alkene.[1] When I first spotted it, I thought not only would it be interesting to do in the lab, but could be extended by incorporating some modern computational aspects as well. 

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References

  1. A. Burke, P. Dillon, K. Martin, and T.W. Hanks, "Catalytic Asymmetric Epoxidation Using a Fructose-Derived Catalyst", Journal of Chemical Education, vol. 77, pp. 271, 2000. https://doi.org/10.1021/ed077p271

Aromatic electrophilic substitution. A different light on the bromination of benzene.

Wednesday, March 12th, 2014

My previous post related to the aromatic electrophilic substitution of benzene using as electrophile phenyl diazonium chloride. Another prototypical reaction, and again one where benzene is too inactive for the reaction to occur easily, is the catalyst-free bromination of benzene to give bromobenzene and HBr. 

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The mechanism of diazo coupling: more hidden mechanistic intermediates.

Saturday, March 8th, 2014

The diazo-coupling reaction dates back to the 1850s (and a close association with Imperial College via the first professor of chemistry there, August von Hofmann) and its mechanism was much studied in the heyday of physical organic chemistry.[1] Nick Greeves, purveyor of the excellent ChemTube3D site, contacted me about the transition state (I have commented previously on this aspect of aromatic electrophilic substitution). ChemTube3D recruits undergraduates to add new entries; Blue Jenkins is one such adding a section on dyes.

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References

  1. S.B. Hanna, C. Jermini, H. Loewenschuss, and H. Zollinger, "Indices of transition state symmetry in proton-transfer reactions. Kinetic isotope effects and Bronested's .beta. in base-catalyzed diazo-coupling reactions", Journal of the American Chemical Society, vol. 96, pp. 7222-7228, 1974. https://doi.org/10.1021/ja00830a009

The wrong trousers: the anti-Markovnikov addition of borane to 2-methylpropene.

Sunday, March 2nd, 2014

A staple of introductory undergraduate teaching in organic chemistry is Markovnikov’s rule, which states: “the addition of a protic acid HX to an alkene results in the acid hydrogen (H) becoming attached to the carbon with fewer alkyl substituents and the halide (X) group to the carbon with more alkyl substituents“. Shortly thereafter, students are exposed to the “anti-Markovnikov” addition of borane to e.g. 2-methylpropene. In order to achieve a consistent explanation for both reactions, I normally show students the following mechanism. Here I introduce a “reality check” to the first component of that mechanism (for the oxidative step, see this post).

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Intersecting paths in molecular energy surfaces.

Sunday, February 16th, 2014

The potential energy surface for a molecule tells us about how it might react. These surfaces have been charted for thousands of reactions using quantum mechanics, and their basic features are thought to be well understood. Coming across an entirely new feature is rare. So what do you make of the following?

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Three-for-one: a pericyclic brain teaser.

Sunday, January 12th, 2014

A game one can play with pericyclic reactions is to ask students to identify what type a given example is. So take for example the reaction below.

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A simple pericyclic reaction encapsulating the four thermal selection rules.

Thursday, January 2nd, 2014

As my previous post hints, I am performing my annual spring-clean of lecture notes on pericyclic reactions. Such reactions, and their stereochemistry, are described by a set of selection rules. I am always on the lookout for a simple example which can most concisely summarise these rules. The (hypothetical) one shown below I think nicely achieves this, and raises some interesting issues in the process.14vs12

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A curly-arrow pushing manual

Wednesday, December 4th, 2013

I have several times used arrow pushing on these blogs. But since the rules for this convention appear to be largely informal, and there appears to be no definitive statement of them, I thought I would try to produce this for our students. This effort is here shared on my blog. It is what I refer to as the standard version; an advanced version is in preparation. Such formality might come as a surprise to some; arrow-pushing is often regarded as far too approximate to succumb to any definition, although it is of course often examined.

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Avoided (pericyclic) anti-aromaticity: Reactions of t-butyl-hydroxycarbene.

Wednesday, November 13th, 2013

Not long ago, I described a cyclic carbene in which elevating the carbene lone pair into a π-system transformed it from a formally 4n-antiaromatic π-cycle into a 4n+2 aromatic π-cycle. From an entirely different area of chemistry, another example of this behaviour emerges; Schreiner’s[1] trapping and reactions of t-butyl-hydroxycarbene, as described on Steve Bachrach’s blog. A point I often make is that chemistry is all about connections, and so here I will discuss such a connection.schreiner

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References

  1. D. Ley, D. Gerbig, and P.R. Schreiner, "Tunneling control of chemical reactions: C–H insertion versus H-tunneling in tert-butylhydroxycarbene", Chem. Sci., vol. 4, pp. 677-684, 2013. https://doi.org/10.1039/c2sc21555a

Kinetic vs thermodynamic enolization.

Tuesday, November 5th, 2013

The concept of kinetic vs thermodynamic control of a reaction is often taught in the context of the enolisation of e.g. 1-methylcyclohexanone as induced by a base. The story goes that at low temperatures (-78°C), the rate of the sterically more hindered thermodynamic enolisation does not compete with the faster kinetic product but that at higher temperatures when an equilibrium is possible, the thermodynamically more stable tetrasubstituted enol is formed. I set out to see if this result can be modelled.

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