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synthesized by reaction with N-p-nitrophenyl-N′-nitrosocarbamide (generated in situ by oxidation of the corresponding hydroxyurea) under anhydrous conditions at ambient temperature or below. When these Diels-Alder adducts are heated under aqueous conditions, they undergo retrocycloaddition to free the diene “cargo”. The released nitroso dienophile hydrolyzes rapidly to produce 4-nitroaniline, nitroxyl (H-N=O), and carbon dioxide (CO2). The rate studies for the decomposition were carried out by warming our
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all my design choices.Lianne Tjoelker BIO Lianne Tjoelker is a senior at Pacific Lutheran University in Tacoma, Washington. She is will be graduating with her Bachelor of Fine Arts in graphic design and a minor in Chinese Studies in the spring of 2017. She plans to pursue her passion for video games by making a career in the video game industry. Lianne has done work and commissions for Pacific Lutheran University’s student run advertising agency, Impact, as well as PLU’s School of Art and Design
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