The other is an SN2 mechanism in which a water molecule to complex catabolism + Co9NH3) 5CL] 2] att

Test 4) The speed of Kvasyvn ion complexation Klrvpntaamyn cobalt (III); despite the large number of complexes containing the ligand H2O we clusion that in some cases may H2O as easily substitute Lygndhayy the Kyvrdynasyvn them is weaker become the such as dimethylsulfoxide (DMSO) as the ligand is. With transition metal ions such as the Ghyat H2o + NI2 through complexation with curing catabolism Dynasyvn but in the presence of oxygen atoms (H2O, (DMSO easily removed and replaced with H2O Kyvrdynasyvn space allows.
Substituted These reactions can be performed by a variety of mechanisms. In this experiment, a CL-Substituted reaction mechanism is determined by H2O review. We will discuss this reaction catabolism in an acidic environment.
A proposed mechanism for this reaction is SN1. Co-CL bond breaking speed at which the rate determining step (slow) catabolism and a vacancy rate of CL-occupied by a molecule of H2O will speed up a law for it is such. (K is the rate constant degree)
The other is an SN2 mechanism in which a water molecule to complex catabolism + Co9NH3) 5CL] 2] attacked and formed catabolism a short-lived intermediate-length sometime soon Kyvrdynh seven CL-your product is lost or created. This is true in the case of the second order rate constant K2 is its speed.
But if your H2O is the solvent concentration catabolism is practically not possible catabolism to determine changes in the amount of H2O that will participate in the reaction, the solvent used, as compared with the total water that is too small in the concentration can be water assumed constant.
This is expected to result in significant F-Kyvrdynh protons by Co-FH bond is weakened so that you can visualize the F-proton HF pulled into a void in space by quickly Kyvrdynasyvn H2O is a molecule Ashghalmy.
If the response is good. Start a stage Kvasyvn catabolism is clear that in the above steps need to know to make the diagnosis. For the next stage, the stage at which the cobalt (III) is low spin and is inert to the reaction, half-life, which is why it was so much more.