scholarly journals The hydrolysis of C12 primary alkyl sulfates in concentrated aqueous solutions. Part 2. Influence of alkyl structure on hydrolytic reactivity in concentrated aqueous mixtures of sodium primary alkyl sulfates: 1-benzoyl-3-phenyl-1,2,4-triazole as a probe of water activity

Author(s):  
Donald Bethell ◽  
Roger E. Fessey ◽  
Jan B. F. N. Engberts ◽  
David W. Roberts
2021 ◽  
Vol 62 (3) ◽  
pp. 350-359
Author(s):  
S. I. Shabunya ◽  
V. G. Minkina ◽  
V. I. Kalinin ◽  
N. D. Sankir ◽  
C. T. Altaf

2003 ◽  
Vol 76 (8) ◽  
pp. 1296-1298 ◽  
Author(s):  
O. A. Kazantsev ◽  
K. V. Shirshin ◽  
A. P. Sivokhin ◽  
S. V. Tel'nov ◽  
I. V. Zhiganov ◽  
...  

1981 ◽  
Vol 36 (6) ◽  
pp. 691-696 ◽  
Author(s):  
Karl-Peter Steinfeldt ◽  
Gert Heller ◽  
Reinhard Baumert

Abstract In the course of the hydrolysis of tris(alkoxy)boranes B(OR)3 (R = methyl, n-butyl, or 2-ethylhexyl) with a small amount of water in organic solvents, both possible intermediates (RO)2BOH and ROB(OH)2 have been unambiguously identified by Raman spectroscopic measurements. Lines have been found for (CH3O)2BOH at 772.8 cm -1 and for CH3OB(OH)2 at 814.6 cm -1 . The compounds are in equilibrium with the starting material B(OCH3)3 and the product B(OH)3.Potentiometrie and conductometric investigations likewise indicate the existence of these species. A mechanism of the hydrolysis reaction is based on kinetic considerations.With hydroxide ions in non-aqueous solvents or aqueous hydroxide ions the hydrolysis reactions occur differently because in the first case the end product of the hydrolysis is the orthoborate ion [B(OH)4]-, whereas in the second case in concentrated aqueous solutions poly borates are formed.


Sign in / Sign up

Export Citation Format

Share Document