Abstract:Notes 627 excess of water is zero. The Gibbsian surface excess will be proportional to the difference between the area under the concentration curve and the area of the rectangle --0-s. For this case it is easy to see that, even though there is a surface layer of solute (positive adsorption at the interface), the Gibbsian surface excess may be positive, zero or negative depending on the concentrations in the double layer region below the interface. It is also plausible that changes in the bulk concentration wi… Show more
“…cis-Piperylene has been shown (21) to react only very slowly with maleic anhydride under the conditions just set forth. The Zrans-isomer reacts rapidly and quantitatively.…”
Section: Conjugated Diolefinsmentioning
confidence: 94%
“…(1600 °F. ), for example (21). Moreover, the piperylenes are removed, in most cases, from trimethylethylene, the closest boiling tertiary mono-olefin, by superfractional distillation, as is pointed out below.…”
“…cis-Piperylene has been shown (21) to react only very slowly with maleic anhydride under the conditions just set forth. The Zrans-isomer reacts rapidly and quantitatively.…”
Section: Conjugated Diolefinsmentioning
confidence: 94%
“…(1600 °F. ), for example (21). Moreover, the piperylenes are removed, in most cases, from trimethylethylene, the closest boiling tertiary mono-olefin, by superfractional distillation, as is pointed out below.…”
“…There appears to be a substantial difference (309) in the rates of addition of maleic anhydride by the cis-and ¿rans-isomers of piperylene. The analysis of a pure mixture of cis-and ¿raras-piperylenes was attempted by Robey and his coworkers, who found that addition ceases between 65 and 78 per cent of completion.…”
Analysis of a simple NMR spectrum is fairly easy and straight forward for undergraduate students but analyzing a fairly complex NMR can be very daunting and requires a methodical approach. This work uses the ubiquitous Diels-Alder reaction of methylcyclopentadiene and maleic anhydride to introduce students to an NMR spectrum that consist of inseparable mixtures of isomers and their analysis using advanced NMR spectroscopic techniques. This laboratory experiment further outlines the use of derivatization techniques for the separation of isomeric mixtures by preparing diastereomers and using NMR spectroscopy for their identification.
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