Organic peroxides containing functional groups. Part II. The reaction of hydrogen peroxide with β- and γ-oxo-acids and esters

1968 ◽  
Vol 0 (0) ◽  
pp. 2983-2986 ◽  
Author(s):  
R. C. P. Cubbon ◽  
C. Hewlett
2007 ◽  
Vol 85 (1) ◽  
pp. 7-11 ◽  
Author(s):  
Mohammad Mehdi Khodaei ◽  
Kiumars Bahrami ◽  
Mohammad Khedri

Hydrogen peroxide together with MoO3 as catalyst can efficiently and chemoselectivity oxidize sulfides to sulfoxides and sulfones in the presence of other oxidized functional groups in ethanol at 50 °C in short reaction times.Key words: oxidation, sulfides, sulfoxides, sulfones, H2O2–MoO3 system.


1964 ◽  
Vol 47 (2) ◽  
pp. 363-366
Author(s):  
James T Taylor

Abstract A quantitative and a qualitative method for the determination of acetone peroxides were subjected to collaborative study. Quantitative analyses are based upon liberation and titration of hydrogen peroxide from acyclic peroxides and hydroperoxides by dilute sulfuric acid and standardized potassium permanganate, respectively. Single determination of 6 samples (varying in per cent levels of peroxide equivalent) each of baking premixes and milling premixes produced very good collaborative results. Qualitative analyses, achieved by comparing infrared spectra of acetone-extracted organic peroxides with acetone-extracted organic peroxides from a reference premix, gave peaks characteristic of the premixes. No interferences were seen from various starch blanks. Both the quantitative and the qualitative methods are recommended for adoption as official, first action.


Fuel ◽  
1994 ◽  
Vol 73 (3) ◽  
pp. 387-395 ◽  
Author(s):  
V GOMEZSERRANO ◽  
M ACEDORAMOS ◽  
A LOPEZPEINADO ◽  
C VALENZUELACALAHORRO

1997 ◽  
Vol 51 (1) ◽  
pp. 74-80 ◽  
Author(s):  
Peter Jacob ◽  
Bernhard Wehling ◽  
Wieland Hill ◽  
Dieter Klockow

The described investigations are focused on peroxides occurring as products in atmospheric chemical processes, namely, hydrogen peroxide, methylhydroperoxide, hydroxymethylhydroperoxide, bis-(hydroxymethyl)peroxide, 1-hydroxyethylhydroperoxide, bis-(hydroxyethyl)peroxide, and hydroxymethylmethylperoxide. The compounds are identified and determined through the position and intensity of their characteristic O–O stretching bands in the range between 767 and 878 cm−1. Time-resolved Raman spectroscopy of peroxide solutions permits the in situ investigation of pathways and kinetics of reactions between peroxides and aldehydes.


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