## Abstract The 1โNH structure for 3โazidoindazole has been demonstrated by the observation of ^1^H๏ฃฟ^1^H and ^13^C๏ฃฟ^1^H couplings involving the hydrogen atom attached to nitrogen. A comparison between 3โazidoindazole and indazole shows that both compounds have the same tautomeric structure.
Determination of the structures and abundances of alkanes and olefins in Fischer-Tropsch products using 13C and 1H n.m.r. methods
โ Scribed by David J. Cookson; Brian E. Smith
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 654 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0016-2361
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โฆ Synopsis
13C and 'H n.m.r. methods are shown to provide detailed and quantitative information regarding the structures and abundances of major and minor hydrocarbon components in products from Fischer-Tropsch synthesis. A test jet fuel product (boiling range 19&230"(Z) has been studied together with a test diesel fuel product (23&32O"C). The jet fuel consists primarily of n-alkanes (87 wt%), while branched alkanes with, on average, 12 carbon atoms per molecule and one CH, branch per molecule, represent another 9wt% of the sample. All possible monomethyl branched alkane isomers are shown to occur with approximately equal probability. Olefins represent nearly 4 wt% of the sample. 13C n.m.r. distinguishes l-ene (0.6 wt%), cis-2-ene (0.8 wt%), trans-2-ene (1.4 wt%), 2-methyl-2-ene (0.4 wt%) and trans-3-ene
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