The terms "endothermic" and "exothermic" refer to whether a chemical reaction absorbs or releases heat, respectively. In an endothermic reaction, heat is absorbed from the surroundings, while in an exothermic reaction, heat is released into the surroundings.
Nuclear decay rates do not vary with the conditions of the change; they are constant for a given isotope. On the other hand, chemical reaction rates can vary with conditions such as temperature, pressure, and the presence of catalysts.
pH and temperature
Reactions with a higher magnitude of standard Gibbs free energy change (ΔG°) tend to occur more rapidly at standard conditions, as it reflects the spontaneity of a reaction. Additionally, reactions with lower activation energy (Ea) values typically proceed more rapidly as they require less energy to initiate the reaction. Ultimately, the rate of a reaction at standard conditions depends on the specific reaction mechanism and kinetics.
A non-spontaneous reaction is typically characterized by requiring a continuous input of energy to proceed and does not occur naturally under standard conditions. It is not driven by an increase in entropy; instead, it often leads to a decrease in entropy. Additionally, non-spontaneous reactions do not have a negative Gibbs free energy change (ΔG > 0). Therefore, they do not occur spontaneously without external intervention.
The terms "endothermic" and "exothermic" refer to whether a chemical reaction absorbs or releases heat, respectively. In an endothermic reaction, heat is absorbed from the surroundings, while in an exothermic reaction, heat is released into the surroundings.
change in concentration change in temperature change in pressure
By heat , the more you add the more it keep going on
Nuclear decay rates do not vary with the conditions of the change; they are constant for a given isotope. On the other hand, chemical reaction rates can vary with conditions such as temperature, pressure, and the presence of catalysts.
pH and temperature
The actual energy change for a reaction might be different from the predicted energy change due to experimental errors, incomplete reactant conversion, side reactions, impurities in reactants, or inaccurate assumptions about reaction conditions. Kinetic factors such as reaction rates and temperature variations during the reaction can also contribute to discrepancies between predicted and actual energy changes.
In thermodynamics, delta G represents the change in Gibbs free energy for a reaction under specific conditions, while delta G degree represents the standard Gibbs free energy change for a reaction under standard conditions.
the heat released or absorbed in a reaction
Hess's law is based on the principle that the enthalpy change of a reaction is independent of the pathway taken. This means that the overall enthalpy change for a reaction is the same, regardless of the number of steps involved in the reaction as long as the initial and final conditions are the same.
If the substance does not change, then it can be assumed that there was no physical or chemical reaction. Depending on what you are trying to accomplish, further testing with different substances or conditions may be necessary.
If the substance does not change, then it can be assumed that there was no physical or chemical reaction. Depending on what you are trying to accomplish, further testing with different substances or conditions may be necessary.
The rate of formation of I2 can be determined by dividing the change in concentration of I2 by the change in time. The specific value would depend on the reaction conditions and rate constants involved in the reaction.