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Original scientific paper

Secondary Hydrogen Isotopes Effects. V. Internal Rearrangement in the Acetolysis of Deuterium Labeled Cyclopropylmethyl Benzenesulfonates

S. Borčić ; Institute »Ruder Boskovic«, Zagreb , Croatia, Yugoslavia
D. E. Sunko ; Institute »Ruder Boskovic«, Zagreb , Croatia, Yugoslavia

Fulltext: english, pdf (5 MB) pages 77-81 downloads: 32* cite
APA 6th Edition
Borčić, S. & Sunko, D.E. (1961). Secondary Hydrogen Isotopes Effects. V. Internal Rearrangement in the Acetolysis of Deuterium Labeled Cyclopropylmethyl Benzenesulfonates. Croatica Chemica Acta, 33 (2), 77-81. Retrieved from https://hrcak.srce.hr/208443
MLA 8th Edition
Borčić, S. and D. E. Sunko. "Secondary Hydrogen Isotopes Effects. V. Internal Rearrangement in the Acetolysis of Deuterium Labeled Cyclopropylmethyl Benzenesulfonates." Croatica Chemica Acta, vol. 33, no. 2, 1961, pp. 77-81. https://hrcak.srce.hr/208443. Accessed 20 Apr. 2021.
Chicago 17th Edition
Borčić, S. and D. E. Sunko. "Secondary Hydrogen Isotopes Effects. V. Internal Rearrangement in the Acetolysis of Deuterium Labeled Cyclopropylmethyl Benzenesulfonates." Croatica Chemica Acta 33, no. 2 (1961): 77-81. https://hrcak.srce.hr/208443
Harvard
Borčić, S., and Sunko, D.E. (1961). 'Secondary Hydrogen Isotopes Effects. V. Internal Rearrangement in the Acetolysis of Deuterium Labeled Cyclopropylmethyl Benzenesulfonates', Croatica Chemica Acta, 33(2), pp. 77-81. Available at: https://hrcak.srce.hr/208443 (Accessed 20 April 2021)
Vancouver
Borčić S, Sunko DE. Secondary Hydrogen Isotopes Effects. V. Internal Rearrangement in the Acetolysis of Deuterium Labeled Cyclopropylmethyl Benzenesulfonates. Croatica Chemica Acta [Internet]. 1961 [cited 2021 April 20];33(2):77-81. Available from: https://hrcak.srce.hr/208443
IEEE
S. Borčić and D.E. Sunko, "Secondary Hydrogen Isotopes Effects. V. Internal Rearrangement in the Acetolysis of Deuterium Labeled Cyclopropylmethyl Benzenesulfonates", Croatica Chemica Acta, vol.33, no. 2, pp. 77-81, 1961. [Online]. Available: https://hrcak.srce.hr/208443. [Accessed: 20 April 2021]

Abstracts
The acetolysis vs. internal rearrangement products ratio was
determined for cyclopropylmethyl, cyclopropylmethyi-1 ,1-dii and
-3,3-d2 benzenesulfonate and was found to remain constant within
the experimental error. The results confirm that both concurrent
reactions proceed through a common intermediate in which the bond
between the carbonium ion and the leaving group must be pureiy
ionic.

Hrčak ID: 208443

URI
https://hrcak.srce.hr/208443

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