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  2. Spontaneous process - Wikipedia

    en.wikipedia.org/wiki/Spontaneous_process

    positive, the process is non-spontaneous as written, but it may proceed spontaneously in the reverse direction. zero, the process is at equilibrium, with no net change taking place over time. This set of rules can be used to determine four distinct cases by examining the signs of the Δ S and Δ H .

  3. Entropy of vaporization - Wikipedia

    en.wikipedia.org/wiki/Entropy_of_vaporization

    This is always positive, since the degree of disorder increases in the transition from a liquid in a relatively small volume to a vapor or gas occupying a much larger space. At standard pressure ⁠ P ⊖ {\displaystyle P^{\ominus }} ⁠ = 1 bar , the value is denoted as ⁠ Δ S vap ⊖ {\displaystyle \Delta S_{\text{vap}}^{\ominus }} ⁠ and ...

  4. Entropy of activation - Wikipedia

    en.wikipedia.org/wiki/Entropy_of_activation

    The value of ΔS ‡ provides clues about the molecularity of the rate determining step in a reaction, i.e. the number of molecules that enter this step. [2] Positive values suggest that entropy increases upon achieving the transition state, which often indicates a dissociative mechanism in which the activated complex is loosely bound and about ...

  5. Second law of thermodynamics - Wikipedia

    en.wikipedia.org/wiki/Second_law_of_thermodynamics

    This is possible provided the total entropy change of the system plus the surroundings is positive as required by the second law: ΔS tot = ΔS + ΔS R > 0. For the three examples given above: 1) Heat can be transferred from a region of lower temperature to a higher temperature in a refrigerator or in a heat pump. These machines must provide ...

  6. Van 't Hoff equation - Wikipedia

    en.wikipedia.org/wiki/Van_'t_Hoff_equation

    From this plot, − ⁠ Δ r H / R ⁠ is the slope, and ⁠ Δ r S / R ⁠ is the intercept of the linear fit. By measuring the equilibrium constant, K eq, at different temperatures, the Van 't Hoff plot can be used to assess a reaction when temperature changes.

  7. Transition state theory - Wikipedia

    en.wikipedia.org/wiki/Transition_state_theory

    At 298 K, a reaction with ΔG ‡ = 23 kcal/mol has a rate constant of k ≈ 8.4 × 10 −5 s −1 and a half life of t 1/2 ≈ 2.3 hours, figures that are often rounded to k ~ 10 −4 s −1 and t 1/2 ~ 2 h. Thus, a free energy of activation of this magnitude corresponds to a typical reaction that proceeds to completion overnight at room ...

  8. Entropy of mixing - Wikipedia

    en.wikipedia.org/wiki/Entropy_of_mixing

    For regular solutions a positive enthalpy of mixing may cause incomplete miscibility (phase separation for some compositions) at temperatures below the upper critical solution temperature (UCST). [ 2 ] : 186 This is the minimum temperature at which the − T Δ S m i x {\displaystyle -T\Delta S_{mix}} term in the Gibbs energy of mixing is ...

  9. Isobaric process - Wikipedia

    en.wikipedia.org/wiki/Isobaric_process

    Restated, the gas does positive work on the environment. If heat is added to the system, then Q > 0. That is, during isobaric expansion/heating, positive heat is added to the gas, or equivalently, the environment receives negative heat. Restated, the gas receives positive heat from the environment. If the system rejects heat, then Q < 0. That ...