Kinetics of redox reaction of lactic acid with bromate ions, and Belousov-Zhabotinskii oscillator with lactic acid

1985 ◽  
Vol 50 (7) ◽  
pp. 1588-1593 ◽  
Author(s):  
Ľubica Adamčíková ◽  
Irena Halinárová
Keyword(s):  
Lactic Acid ◽  
Induction Period ◽  
Redox Reaction ◽  
Kinetic Data ◽  
Activation Parameters ◽  
Oscillation Period ◽  
Probable Mechanism ◽  
Hydrogen Ions ◽  
First Order ◽  
Kinetics Of

The kinetics and mechanism of the redox reaction of bromate ions with lactic acid was studied in the medium of sulphuric acid. The reaction is of first order with respect to both reactants. The dependence of the measured rate constant on the concentration of hydrogen ions was analysed and the activation parameters of the reaction were determined. Based on the experimental kinetic data, the probable mechanism is discussed. Oscillations of bromine and catalyst are observed in the system KBrO3-CH3CHOHCOOH-H2SO4-MnSO4 if the solution is bubbled with nitrogen. The dependence of the induction period and oscillation period on the concentration of the reactants was evaluated.

scholarly journals Kinetics and mechanism of the C-S coupling reactions of aryl Grignard reagents with aryl arenesulfonates

2008 ◽  
Vol 6 (2) ◽  
pp. 237-244 ◽  
Author(s):  
Ender Erdik ◽  
Fatma Eroğlu
Keyword(s):  
Nucleophilic Addition ◽  
Kinetic Data ◽  
Grignard Reagent ◽  
Activation Parameters ◽  
Grignard Reagents ◽  
Coupling Reactions ◽  
Sulfonyl Group ◽  
First Order ◽  
Kinetics Of ◽  
Hammett Relationship

AbstractThe kinetics of the C-S coupling of arylmagnesium bromides with phenyl tosylate has been studied in THF: toluene at 90°C. The reaction is first order in Grignard reagent and first order in phenyl tosylate. Kinetic data, Hammett relationship and activation parameters are consistent with a nucleophilic addition mechanism involving rate determining attack of carbanion to sulfonyl group followed by a fast phenoxide group leaving.

Kinetics of oxidation of α-ketoglutaric acid with Ce(IV) ions in relation to Belousov-Zhabotinskii reaction

1982 ◽  
Vol 47 (11) ◽  
pp. 2831-2837 ◽  
Author(s):  
Ľudovít Treindl ◽  
Vasil Dorovský
Keyword(s):  
Redox Reaction ◽  
Platinum Electrode ◽  
Activation Parameters ◽  
Enol Form ◽  
Kinetics Of Oxidation ◽  
First Order ◽  
Redox Catalyst ◽  
Oscillation Reaction ◽  
Belousov Zhabotinskii Reaction ◽  
Kinetics Of

Oxidation of α-ketoglutaric acid with Ce(IV) ions in a solution of sulphuric acid is a reaction of the first order with respect to both Ce(IV) ions and substrate, is acid catalysed, and its rate is proportional to the reciprocal square of the equilibrium HSO4- concentration. From the temperature dependence of the rate constant in 1.5M-H2SO4, the activation parameters were determined as ΔH##f = 57 kJ/mol and ΔS##f = -45 J mol-1 K-1. The redox reaction proper consists apparently of two steps: in the first one, the enol form of α-ketoglutaric acid reacts with Ce(IV) ions with the formation of the corresponding radical; in the second one, the latter is oxidized further with Ce(IV) to give malonic and succinic acids. Conditions are indicated under which α-ketoglutaric acid serves as substrate for the Belousov-Zhabotinskii oscillation reaction in the presence of Ce(IV)-Ce(III) redox catalyst. Oscillations of Ce(IV) and Br2 concentrations, shifted in phase, can be recorded polarographically with a rotating platinum electrode.

Kinetics and mechanism of oxidation of lactic acid by KMnO4 in H2SO4 medium

1985 ◽  
Vol 63 (12) ◽  
pp. 3317-3321 ◽  
Author(s):  
M. M. Girgis ◽  
S. A. El-Shatoury ◽  
Z. H. Khalil
Keyword(s):  
Lactic Acid ◽  
Oxidation Rate ◽  
Arrhenius Equation ◽  
Activation Parameters ◽  
Initial Oxidation ◽  
Kinetics Of Oxidation ◽  
First Order ◽  
Acid Catalyzed ◽  
Mechanism Of Oxidation ◽  
Kinetics Of

The initial oxidation stages of lactic acid by acid permanganate were investigated. The rate of the induction period was slow and then gradually increased. The kinetics of oxidation were second order, first order with respect to both lactic acid and Mn(VII). The reaction was acid catalyzed. Addition of Mn(II) ions largely increased the rate of the initial stages and decreased the rate of the following stages. The oxidation rate was decreased by the addition of F− or [Formula: see text] ions. The Arrhenius equation was valid for the reaction between 16.5 and 34 °C. Activation parameters were evaluated and a mechanism consistent with the results obtained was proposed.

scholarly journals Kinetics and Mechanism of Oxidation of Benzyl Alcohol by Benzimidazolium Fluorochromate

2008 ◽  
Vol 5 (4) ◽  
pp. 754-760
Author(s):  
J. Dharmaraja ◽  
K. Krishnasamy ◽  
M. Shanmugam
Keyword(s):  
Benzyl Alcohol ◽  
Sodium Perchlorate ◽  
Activation Parameters ◽  
Aqueous Acetic Acid ◽  
Hydrogen Ions ◽  
Acetic Acid Medium ◽  
Kinetics Of Oxidation ◽  
First Order ◽  
Oxidation Of Benzyl Alcohol ◽  
Kinetics Of

The kinetics of oxidation of benzyl alcohol (BzOH) by benzimidazolium fluorochromate (BIFC) has been studied in 50% aqueous acetic acid medium at 308 K. The reaction is first order with respect to [oxidant] and [benzyl alcohol]. The reaction is catalysed by hydrogen ions. The decrease in dielectric constant of the medium increases the rate of the reaction. Addition of sodium perchlorate increases the rate of the reaction appreciably. No polymerization with acrylonitrile. The reaction has been conducted at four different temperature and the activation parameters were calculated. From the observed kinetic results a suitable mechanism was proposed.

Kinetics and Mechanism of Hexachloroiridate(IV) Oxidation of Arsenic(III) in Acidic Perchlorate Solutions

1992 ◽  
Vol 57 (7) ◽  
pp. 1451-1458 ◽  
Author(s):  
Refat M. Hassan
Keyword(s):  
Ionic Strength ◽  
Fractional Order ◽  
Activation Parameters ◽  
Order Reaction ◽  
First Order Reaction ◽  
Intermediate Complex ◽  
Constant Ionic Strength ◽  
Kinetics Of Oxidation ◽  
First Order ◽  
Kinetics Of

The kinetics of oxidation of arsenic(III) by hexachloroiridate(IV) at lower acid concentrations and at constant ionic strength of 1.0 mol dm-3 have been investigated spectrophotometrically. A first-order reaction in [IrCl62-] and fractional order with respect to arsenic(III) have been observed. A kinetic evidence for the formation of an intermediate complex between the hydrolyzed arsenic(III) species and the oxidant was presented. The results showed that decreasing the [H+] is accompanied by an appreciable acceleration of the rate of oxidation. The activation parameters have been evaluated and a mechanism consistent with the kinetic results was suggested.

The kinetics of the decarboxylation of β-resorcylic acid in catechol

1976 ◽  
Vol 29 (2) ◽  
pp. 443 ◽  
Author(s):  
MA Haleem ◽  
MA Hakeem
Keyword(s):  
Rate Equation ◽  
Kinetic Data ◽  
Reaction Rate ◽  
Complex Mechanism ◽  
First Order ◽  
Absolute Reaction Rate ◽  
First Time ◽  
Kinetics Of ◽  
Absolute Reaction ◽  
Reaction Rate Equation

Kinetic data are reported for the decarboxylation of β-resorcylic acid in resorcinol and catechol for the first time. The reaction is first order. The observation supports the view that the decomposition proceeds through an intermediate complex mechanism. The parameters of the absolute reaction rate equation are calculated.

scholarly journals Reactivity of Phenol and Aniline towards Quinolinium Chloro Chromate: A Comparative Oxidation Kinetic Study

2015 ◽  
Vol 59 ◽  
pp. 81-92
Author(s):  
Seplapatty Kalimuthu Periyasamy ◽  
H. Satham Hussain ◽  
R. Manikandan
Keyword(s):  
Oxidation Kinetic ◽  
Activation Parameters ◽  
Dipole Interaction ◽  
Reaction Rates ◽  
Hydrogen Ion ◽  
Aqueous Acetic Acid ◽  
Acetic Acid Medium ◽  
First Order ◽  
Different Temperatures ◽  
Kinetics Of

The kinetics of Oxidation of Phenol and aniline by quinolinium Chlorochromate (QCC) in aqueous acetic acid medium leads to the formation of quinone and azobenzene respectively. The reactions are first order with respect to both Phenol and aniline. The reaction is first order with respect to quinolinium chlorochromate (QCC) and is catalyzed by hydrogen ion. The hydrogen-ion dependence has the form: kobs = a+b [H+]. The rate of oxidation decreases with increasing dielectric constant of solvent, indicating the presence of an ion-dipole interaction. The reaction does not induced the polymerization of acrylonitrile. The retardation of the rate by the addition of Mn2+ ions confirms that a two electron transfer process is involved in the reaction. The reaction rates have been determined at different temperatures and the activation parameters have been calculated. From the above observations kinetic results a probable mechanism have been proposed.

scholarly journals The alcoholysis of 1,2,2-trimethylpropyl-methylfluorophosphonate

2000 ◽  
Vol 65 (12) ◽  
pp. 857-866
Author(s):  
Mladjen Micevic ◽  
Slobodan Petrovic
Keyword(s):  
Kinetic Data ◽  
Reaction Rate ◽  
Frequency Factor ◽  
Reaction Rate Constant ◽  
Order Reaction ◽  
Activation Entropy ◽  
Second Order Reaction ◽  
Third Order ◽  
First Order ◽  
Kinetics Of

The alcoholysis of 1,2,2-trimethylpropyl-methylfluorophosphonate (soman) was examined with a series of alkoxides and in corresponding alcohols: methanol, ethanol, 1-propanol, 2-propanol, 2-methoxyethanol and 2-ethoxyethanol. Soman reacts with the used alkoxides in a second order reaction, first order in each reactant. The kinetics of the reaction between 1,2,2-trimethylpropyl-methylfluorophosphonate and ethanol in the presence of diethylenetriamine was also examined. A third order reaction rate constant was calculated, first order in each reactant. The activation energy, frequency factor and activation entropy were determined on the basis of the kinetic data.

scholarly journals Notizen: Kinetics of the Oxidation of Acetaldehyde by Manganese(III) Sulphate

1974 ◽  
Vol 29 (9-10) ◽  
pp. 691-693 ◽  
Author(s):  
M. S. Murdia ◽  
R. Shanker ◽  
G. V. Bakore
Keyword(s):  
Activation Parameters ◽  
First Order ◽  
Kinetics Of ◽  
Direct Attack

Oxidation of acetaldehyde with manganese(III)- sulphate is first order with respect to acetaldehyde and the oxidant. The rate is independent of acidity (2.0 > [H+] < 5.0 ᴍ and initial [Mn(II)]. Formaldehyde is one of the products of oxidation. Activation parameters for the reaction have been evaluated. The rate of enolisation under similar conditions is less than the rate of oxidation. A mechanism involving a direct attack on the aldehyde by Mn(III) has been suggested.

Kinetics and Activation Parameters for the Alkaline Aqueous Rearrangement of Trichorfon [O,O-Dimethyl-(2,2,2-Trichloro-1-Hydroxyethyl) Phosphonate] to Dichlorvos [O,O-Dimethyl-O-(2,2-Dichloroethenyl)Phosphate]

2001 ◽  
Vol 36 (3) ◽  
pp. 589-604 ◽  
Author(s):  
Julian M. Dust ◽  
Christopher S. Warren
Keyword(s):  
Activation Energy ◽  
High Pressure ◽  
Activation Parameters ◽  
Base Catalysis ◽  
Rearrangement Product ◽  
Exponential Factor ◽  
First Order ◽  
Pseudo First Order ◽  
Order Plot ◽  
Kinetics Of

Abstract The kinetics of the alkaline rearrangement of O,O-dimethyl-(2,2,2-trichloro-1- hydroxyethyl)phosphonate, (trichlorfon, 1), the active insecticidal component in such formulations as Dylox, was followed at 25±0.5°C by high pressure liquid chromatography (UV-vis detector, 210 nm). The rearrangement product, O,Odimethyl- O-(2,2-dichloroethenyl)phosphate (dichlorovos, 2), which is a more potent biocide than trichlorfon, undergoes further reaction, and the kinetics, consequently, cannot be treated by a standard pseudo-first-order plot. A two-point van't Hoff (initial rates) method was used to obtain pseudo-first-order rate constants (kѱ) at 25, 35 and 45°C: 2.6 × 10-6, 7.4 × 10-6 and 2.5 × 10-5 s-1, respectively. Arrhenius treatment of this data gave an activation energy (Ea) of 88 kJ·mol-1 with a pre-exponential factor (A) of 5.5 × 109 s-1. Kinetic trials at pH 8.0 using phosphate and tris buffer systems show no buffer catalysis in this reaction and indicate that the rearrangement is subject to specific base catalysis. Estimates are reported for pseudo-first-order half-lives for trichlorfon at pH 8.0 for environmental conditions in aqueous systems in the Corner Brook region of western Newfoundland, part of the site of a recent trichlorfon aerial spray program.

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