The kinetic energy distribution of D + ions resulting from the interaction of a femtosecond laser pulse with D2 molecules is calculated based on the rescattering model. From analyzing the molecular dynamics, it is shown that the recollision time between the ionized electron and the D + 2 ion can be read from the D + kinetic energy peaks to attosecond accuracy. We further suggest that more precise reading of the clock can be achieved by using shorter fs laser pulses (about 15fs).PACS numbers: 34.50. Rk, 31.70.Hq, 95.55.Sh Human experience shows that new areas of science and technology open up with the ability to make measurements at increasingly shorter time regime. With the advent of femtosecond (fs) lasers, femtochemistry became possible where chemical reaction dynamics can be probed at the atomic scale [1]. Clearly, fs lasers cannot be used directly to probe electron dynamics which is in the attosecond (as) regime. While a substantial effort is being dedicated to developing single attosecond pulses [2,3,4,5], presently few laboratories have such lasers available.An ingenious suggestion for performing measurements at attosecond resolution with fs lasers was proposed by Corkum and his group recently. Their results were reported in two recent publications, here to be called I [6] and II [7], respectively. In their experiment, a 40 fs pulse, with mean wavelength ranging from 800 nm to 1850 nm, and peak intensity of about 1.5 × 10 14 W/cm 2 , was used to ionize a D 2 molecule to produce D + ion. It was assumed that D 2 was first ionized near the peak of the laser pulse to create a correlated electronic and nuclear wave packet. Within a single optical cycle, the electron was driven back to collide with D + 2 and to excite it to the excited σ u electronic state which subsequently dissociated to produce D + . The kinetic energy of the D + ion reflects the internuclear distance, as well as the time when the rescattering occurs. With proper laser intensity, both the initial ionization and the rescattering are found to occur at time interval of far less than one optical cycle, thus providing attosecond temporal resolution, irrespective of the femtosecond pulse duration of the laser. In II, by changing the wavelength of the fs laser, they concluded that the dissociation dynamics of D + 2 can be used as a molecular clock and the clock can be read with attosecond resolution.To read the molecular clock accurately, the rescatter- * Contact: xmtong@phys.ksu.edu ing mechanism which leads to the measurable D + kinetic energy distribution has to be understood in details. In this Letter we report the main conclusion of our careful analysis of the rescattering mechanism. In contradiction to I and II, our analysis shows that the D + ions are not produced by the dissociation of the excited D + produced from Coulomb explosion vs. from dissociation was determined. Our analysis also shows that the dominant peak of the D + kinetic energy distribution is from the third return of the rescattering process, rather than from the first retu...