scholarly journals Chemical Reactions, Reactions in Aqueous Solution, and Oxidation Reduction Reactions, Review II (Weyh, J. A.; Crook, J. R.; Hauge, L. N.)

1989 ◽  
Vol 66 (6) ◽  
pp. A172
Author(s):  
William F. Coleman
2021 ◽  
pp. 365-388
Author(s):  
Christopher O. Oriakhi

Oxidation and Reduction Reactions deals with chemical reactions involving electron transfer. It begins with oxidation numbers and their applications in naming complex molecular or ionic compounds. Rules for assigning oxidation numbers and how to calculate the oxidation number of any atom in a compound or ion are described. Extensive coverage is given to oxidizing and reducing agents, including how to identify them in a given process. Half-cell reactions are defined. Balancing redox equations with the oxidation number method and the half-reaction method are emphasized. The chapter concludes with an overview of oxidation-reduction titration and calculations based on redox titration analysis.


1960 ◽  
Vol 29 ◽  
pp. 49 ◽  
Author(s):  
W. C. E. Higginson ◽  
D. R. Rosseinsky ◽  
J. B. Stead ◽  
A. G. Sykes

1994 ◽  
Vol 59 (3) ◽  
pp. 549-557
Author(s):  
František Skopal ◽  
Václav Dušek

Theoretical relationships and simplifying conditions have been derived for the feed of two reaction components into a nonisochoric reactor with ideal stirring. The feed of reaction components is controlled by the negative feedback at a constant absorbance of the reaction mixture. The theoretical relationships have been verified using model 2. order oxidation-reduction reactions of Ce(IV)/V(IV) and Fe(III)/V(III) in 1 M sulfuric acid at 20 °C.


2020 ◽  
Vol 85 (2) ◽  
pp. 464-466
Author(s):  
Kenzo Yokozeki ◽  
Isao Abe

ABSTRACT Here, we report a novel industrial aspartame production route, involving the enzymatic production of α-l-aspartyl-l-phenylalanine β-methylester from l-aspartic acid dimethylester and l-phenylalanine by α-amino acid ester acyl transferase. The route also involves the chemical transformation of α-l-aspartyl-l-phenylalanine β-methylester to α-l-aspartyl-l-phenylalanine methylester hydrochloride (aspartame hydrochloride) in an aqueous solution with methanol and HCl, followed by HCl removal to form aspartame.


1958 ◽  
Vol 19 ◽  
pp. 10-11 ◽  
Author(s):  
Balwant Singh ◽  
Sardul Singh

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