Kumar, Anil

Srivastava, S. P.

English

NOPR

indian Journal of ChemistryVol. 15A, December 1977, pp. 1061-1065Kinetics & Mechanism of Ag+-catalysed Oxidation of Glycerol byPeroxydisulphate-An Analysis of Consecutive ReactionsS. P. SRIVASTAVA & ANIL KUMARChemical Laboratories, University of Roorkee, Roorkee 247672Received 25 November 1976; revised 6 April 1977; rereuised and accepted 8 September 1977A~+-catalysed oxidation of ilycerol by peroxydisulphate has been found to yield formalde-hyde and ~lycolaldehyde by a first order process in the first stage, which is followed by theoxidation of the two aldehydes to yield formic and ~lycollic acids respectively by two indepen-dent first order reactions. A complete analysis of the two consecutive reactions has been madeand the products have been characterized. The above ftndtngs are different from those reportedpreviously for this reaction [J. Indian chern, Soc., 41 (1964), 402].MISHRA and Ghosh! earlier showed that likeother Ag+-catalysed .oxidations by S20ij-, o:xi-dation of glycerol IS also first order Withrespect to oxidant and catalyst Ag", and is ofzero order with respect to glycerol. They identifiedformaldehyde, acetaldehyde, formic acid and aceticacid as the products of oxidation. However, neitherany kinetic evidence was put forth for the formationof these compounds by side or consecutive reactionsnor the reaction sequence worked out. It appearsthat this reaction, unlike the oxidations of otherorganic substrates by S20:- is a complex reactionconsisting of side as well as consecutive reactions.In view of this we were prompted to reinvestigatethis reaction to study the influence of side andconsecutive reaction on the overall kinetics, and toidentify the oxidation products. The uncatalysedoxidation of glycerol by peroxydisulphate has beenreported by Vasudeva and Wasif>,Materials and MethodsAll the chemicals used were of AR quality.Potassium peroxydisulphate was used after recrystal-lization.The progress of the reaction was followed byestimating the unreacted K2S208 iodometrically bythe method of Szabo, Csanyi and Galiba" as modifiedby Khulbe and Srivastava",The progress of the reaction was also followedkinetically by estimating the amount of totalaldehyde formed" as well as the amount of formal-dehyde formed by spectrophotometric method". Inthe above method the reaction was quenched by theaddition of 5 ml of a saturated solution of KCI ineach aliquot of 5 ml and centrifuged before applyingthe spectrophotometric method.Results and DiscussionProduct analvsis and stoichiometry - Formaldehydeand glycolaldehyde were detected in the reactionmixture in earlier stages of the reaction by chromo-tropic acid test and diphenylamine test", respectively.0.51 , Io 10I20I30It may be noted that acetaldehyde is not formedas reported by Mishra and Ghosh", This erroneousfinding might perhaps have been due to the sodiumnitroprusside and morpholine test used to characte-rize acetaldehyde which is also positive for glycol-aldehyde. Further confirmation of the presence ofglycolaldehyde is provided by a study of the NMRand IR spectra of 2,4-diphenylhydrazone of theTLC separated product. Further, the presence of ahydroxy acid (obviously glycollic acid) detectedin the later stages of the reaction by sym. 1,5-di-phenyl carbazide test" confirms the formation ofglycolaldehyde in the earlier stage.The total amount of aldehvde formed at variousintervals of time was estimated spectrophotometri-cally- at 560 urn (characteristic of the complexbetween Schiff's reagent and the aldehyde at pH2·7). The amount of formaldehyde at differentintervals of time was also estimated spectrophoto-metrically but with the help of sodium salt ofchromotropic acid at 570 nm", The amount ofglycolaldehyde was evaluated by difference. Thequantities of aldehydes formed at three differenttemperatures are recorded in Table 1. It is apparentfrom T<;tble 1 th~t the oxidation of glycerol byperoxydisulphate IS a case of consecutive reactionsince the [total aldehyde] starts decreasing after acertain interval of time. Formaldehyde and glycol-aldehyde are formed nearly in equimolar amounts.The mole ratio in the first stages of the reactionup to the formation of aldehydes has been foundto .be equal for ~he glycerol-peroxydisulphate re-action. The maximum yield in terms of totalaldehyde formation is 85% at 35°.Kinetic behaviour - The results of typical kineticruns at three different temperatures followed bv theestim~tion of the unr~acted peroxydisulphate aregraphically presented In Fig. 1. In these kineticruns five-fold excess of S20~- has been employedso as to study the next stage of the reaction also.It aI?pears from the data in Fig. 1 that the reactionconsists of two first order consecutive reactions,1061I40 50Timt' in ""nut~I60I70I80,00Fig. 2 - Plot of amount of HCHO formed versus time (t) at different temperatures ([Glycerol) = O'OlM; [K1StOa]= O·OSM; [AgN03J = O'OO1M}1063INDIA~ J. CHEM., VOL. 1M, DECEMBER 1977TABLE 1 - ,\MOLTNTSOF FORMALDEHYDEAND GLYCOLALDEHYDEFORMEDAT DIFFERENT STAGESOF REACTIONAND ATDIFFERENT TEMPERATURES{[Glycerol] = O'OtM; [K2S20.] = O'OSM; [AgNOa] = O·OOlM}Time Temp. 35°C Temp. 40°C Temp. 4ScCmm [Total [HCHO} [Glycol- [Total [HCHO) [Glycol- [Total [HCHO] [Glycol-aldehyde] (Mx 103) aldehyde] aldehyde] (M x 103) aldehyde) aldehyde] (M x toa) aldehyde](.\1 x 103) (Mx 103) (M x t03) (M x 10") (Mx 10') (MxW)5 1·12 0·57 0'55 1·29 0'64 0·65 1·66 0·12 0·94to 2·71 1·42 4·29 2·56 1·56 t·OO 3'41 2·06 1·3515 3·58 1·98 1·60 4·46 2·41 2·05 4·75 2'90 1-8520 4·61 2·55 206 5·40 2·94 2·47 3·6825 5·41 6·37 3·61 2·76 6·8230 6·20 3·33 2·87 7·16 4·11 3·05 7·37 4·53 2'8435 7·3740 7·39 4·11 3·28 7·64 4·85 2·79 6·9850 7·91 4·61 3·30 8·27 4·99 3·28 5'39 3'47 1·9260 8·58 4·89 3·69 7·00 4·99 2·01 2·7770 8'58 5·73 08775 5:17 HI80 8·4290 7·79 4-82 2·971.49Iv'''f (Glycerol J -2: 1.0 x 10 MF 1.41~ (K25208) -2: 5.0 x 10 M-'3(AqN03 J : 1.0 x 10 M1.37Curve no. Temp.oC111 35121 401.33 131 451.51.611.53Time in minutesFig. 1 - Plots of log C versus time (I) at different temperatures {[Glycerol] = O'OlM: [K1S10.] = O'05M; [AgNOaJ = O.OOlM}1062SRIVASTAVA & KUMAR: OXIDATION OF GLYCEROL BY PEROXYDISULPHATETemp.°CTABLE 2 - SPECIFIC RATES OF OXIDATION OF REACTIONS (A) AND (B){[Glycerol] = 0·01111; [K.S.Osl = 0·05111; [Ag~03] = O·OOLU}k(a) k(b) k(c) Sp. rate (kf)(d) Sp. rate (k~)(e) ex (Mx103) c, (Mx101)1 1 2(litres (litres (litres of oxidn of of oxidn ofmol"! mol"! mol-l HCHO glycolaldehyde Obs. Calc. Obs, Calc.mirr '} rnirr+) mirr+) (litres (litresmol-l min-I) mol'! min-I)4·96 6·40 8·30 4·95 3·35 5·17 3·14 3·70 2·876·47 8·36 13·65 5·43 8·22 4·99 3·15 3·28 2·548·42 11·76 21·82 6·28 15'54 4·53 2·63 2·84 2·45354045(a) Refers to rate of consumption of S20~- (reaction-A). (b) Refers to rate of formation of formaldehyde (reaction-A).(c) Rate of oxidation of aldehydes. (d) [HCHO] = 0·005111; [S20i-] = 0·05111; [Ag+l = 0·001M. (e) Refers to rate ofoxidation of glycolaldehyde (reaction-B).1.3-oc 2.52E1:'t;c(3 2.14.94.54.11"1$23.7"~'Lo] 3.3.s'"-0~~ 2.90E.E1.7Curve no. _III121131Temp. 1°03540450.9Fig. 2 - Plot of amount of HCHO formed versus time (I) at different temperatures {[Glycerol] = 0'01M; [K.S.OaJ= 0'05M; [AgNOaJ = O'OOlM}10633.0Q"~.;:.!ZoEc::INDIAN J. CHEM., VOL. ISA, DECEMBER 19771.0 Cu~no. _II)(2)(3)Temp.l"O354045Fig.! 3 - Amount of glycolaldehyde formed versus time (t) at different temperatures {[Glycerol] = Q·QIM; [K.S.O.J= O'OSM; [AgNOsl = Q'OOlM}designated as A and B. The specific rate (k1)for the reaction-A was computed by estimating theamount of formaldehyde formed at different intervalsof time and on the basis that one' molecule ofglycerol gives one molecule of formaldehyde andone molecule of glycolaldehyde. The specific rate(k1 or k2) reported was obtained by dividing theobserved rate constant by the [Ag+] employed ascatalyst, i.e. kl or k2 = kobs /[Ag+J.A perusal of the results given in Table 2 showsthat the specific rate (k1) for the reaction-A byformaldehyde determination and by peroxydisulphateconsumption are of the same order of magnitude.In reaction-B the two aldehydes formed are gettingoxidized into their products through two independentreactions. The specific rate for formaldehyde oxida-tion (k~) into formic acid was determined separatelyalso under identical conditions by taking formal-dehyde nearly equal to the maximum amount,c,.(max) obtained in glycerol oxidation. The specificrate (k;) for glycolaldehyde oxidation was thenevaluated by subtracting k~ from the specific ratek2 for second stage of oxidation of glycerol, assumingthat the second stage consists of two parallel firstorder reactions. The values of k~ and k; thusobtained were used to calculate the value of1064maximum concentration of formaldehyde, Gz(max)and glycolaldehyde, G,,(max) formed in the glyceroloxidation by employing the expressions (1) and (2)akGz(max) = _,_1_ [e-k,l -e k;t] ... (1)k2-k1G,,(max) = k:k1k [e-k,t -e-k;t] ... (2)2- 1The amounts of formaldehyde and glycolaldehydeformed at various intervals of time (as given inTable 1), when plotted against time (Figs. 2 and 3)gave characteristic curves for consecutive reactions.The values of Gz(max) a1trl G,,(max) extrapolatedfrom these curves are tabulated along with thecalculated values in Table 2. Taking into accountthe possible errors in such estimations, there seemsto be rather good agreement between the calculatedand observed values.The energy parameters for reaction-A as calculatedfrom the rate constant values are of the sameorder of magnitude as those reported by Mishraand Ghosh".Mechanism - On the basis of the above resultsthe different stages of the Ag+-catalysed peroxy-disulphate oxidation of glycerol may be representedas shown in Scheme 1.SRIVASTAVA & KUMAR: OXIDATION OF GLYCEROL BY PEROXYDlSULPHATEklCH.OH.CHOH.CHpH -+ HCHO + CHO.CH.OHI I1k. II k;HCOOH ~COOH.CH20HScheme 1Taking into account the general similarity inkinetic behaviour of this reaction with other Ag+-catalysed redox reactions of S20~-, we propose thereaction mechanism shown in Scheme 2 for thefirst stage of the Ag+-catalysed oxidation of glycerol.hIAg++S20~- ---+ Ag2++S0l-+S04- ... (i)k,S04-+H20 ---+ HS04+'OH ... (ii)k.S+'OH ---+ HCHO+R+H20 ... (iii)»,S+Ag2+ ---+ HCHO+H++Ag++R ... (iv)k,R+S20~- --+ HS04+S0i-+CHO.CH20H ... (v)k,R+S04- ----J>. HSOi+CHO.CH20Hwhere S stands for glycerol andCHOH.CH20H.... (vi)R stands forScheme 2Applying steady state treatment to the radicalsS04-' 'OH, Ag2+ and R the rate expression for theconsumption of peroxydisulphate comes out to be_ d[S;~~-J = kl [Ag+][S20~-] + Cl::k5y/2[S20~-J [Ag+]1/2Since ke'}>kl or k2 or ks' because ke refers to aradical-radical reaction, hence the second term ismuch smaller than the first term and kineticallynot distinguishable and apparently the reactionfollows first order behaviour in [S20~-] and [Ag+J.It is pertinent to point out that the first twostages· have been proposed by a large number ofworkerss-13 and the hydrogen abstraction from theorganic substrate to yield the radical is consideredto be the next probable step. The existence ofS04- and 'OH in peroxydisulphate redox reactionshas recently been proved by the ESR studies ofChawla and Richard-s while the formation of Ag2+in peroxydisulphate redox processes has been shownby the ESR studies of McMillan and Smaller'>.AcknowledgementOne of the authors (A.K.) is thankful to theCSIR, New Delhi, for awarding a junior researchfellowship to him.References1. MISHRA, D. D. & GHOSH, S., J. Indian chem. Soc., 41(1964), 402.2. VASUDEVA, W. C. & WASIF, S., J. chem. Soc., B5 (1970),960.3. SZABO, Z. G., CSANYI, L. & GALIBA, H., Z. analyt, Chem.,135 (1952), 269.4. KHULBE, K. C. & SRIVASTAVA, S. P., Agra Univ. J.Res. (Sci.), 9 (1960), 177; 14 (1965), 85.5. Organic analysis, Vol. I, edited by John Mitchell (Jr),1. :Vl. Kolthoff, E. S. Proskauer & A. Weissberger(Interscience, New York), 1961, 286.6. DISCHE, E. & BORENFREUND, E., J. biol, Chem., 180(1949), 1297.7. Spot test in organic analysis, edited by F. Feigl (Elsevier,Amsterdam), 1966, 627.8. SRIVASTAVA, S. P. & GHOSH, S., Proc. nain, A cad. su.,22 (1953), 91; 23 (1954), 44.9. BAWN, C. E. H. & MARGERISON, D., Trans. Faraday Soc.,51 (1955), 925.10. BHAKUNI, R. S. & SRIVASTAVA, S. P., Z. phys. cso«,210 (1954), 246. .11. KHULBE, C. P. & SRIVASTAVA, S. P., Agra Univ. J. Res.(Sci.), 15 (1969), 27.12. KHAN, M. :VI.& SRIVASTAVA, S. P., J. Indian chem. Soc.,46 (1969), 574.13. SRIVASTAVA, S. P. & SINGHAL, S. K., J. Indian chem,Soc., 46 (1969), 705.14. CHAWLA, OM. P. & RICHARD, W. FESSENDEN, J. phys.cu-«, 79 (1975), 2693.IS. McMILLAN, J. A. & SMALLER, B., J. chem. Phys., 35(1961), 1698.1065

Kinetics & Mechanism of Ag+-catalysed Oxidation of Glycerol by Peroxydisulphate-An Analysis of Consecutive Reactions

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Kinetics & Mechanism of Ag+-catalysed Oxidation of Glycerol by Peroxydisulphate-An Analysis of Consecutive Reactions

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