The Gibbs free energy change (ΔG) for a reaction is always positive when the reaction is non-spontaneous under the given conditions. This typically occurs at high temperatures for exothermic reactions (where ΔH is negative and ΔS is positive) or when the entropy change (ΔS) is negative while ΔH is positive. In such cases, the term TΔS is not large enough to overcome the positive ΔH, resulting in a positive ΔG.
Delta G (Gibbs free energy change) for a reaction is always positive when the reaction is non-spontaneous under the given conditions. This typically occurs when the system is at equilibrium or when the enthalpy change (ΔH) is positive and the entropy change (ΔS) is negative, leading to a situation where the temperature multiplied by ΔS (TΔS) is not sufficient to drive the reaction forward. Additionally, when the reactants are more stable than the products, or when the reaction requires external energy input to proceed, delta G will also be positive.
A positive value of delta G (ΔG) indicates that a reaction is non-spontaneous under standard conditions, meaning it requires an input of energy to proceed. In this case, the products have higher free energy than the reactants, suggesting that the reaction is unfavorable in its current direction. Therefore, the reaction is more likely to occur when coupled with a spontaneous process or under different conditions that favor the formation of products.
A positive value of G0 (standard Gibbs free energy change) indicates that the reaction is non-spontaneous under standard conditions. This means that, at standard temperature and pressure, the reactants are favored over the products, and the reaction will not proceed in the forward direction without the input of energy. In practical terms, it suggests that the reaction is thermodynamically unfavorable.
A redox reaction with a positive standard electrode potential indicates that the reaction is spontaneous under standard conditions. This means that the tendency for the reduction half-reaction to occur is favored, making it more likely for the oxidizing agent to gain electrons. In practical terms, such reactions can drive processes like electrochemical cells, where energy is harnessed from the spontaneous electron transfer. Thus, a positive potential signifies a favorable thermodynamic outcome for the reaction.
A positive cell potential indicates that the redox reaction is spontaneous under standard conditions. This means that the reactants have a higher free energy than the products, leading to a favorable reaction that can occur without external energy input. Additionally, it suggests that the reduction half-reaction has a greater tendency to gain electrons compared to the oxidation half-reaction losing them.
When H is positive and S is negative
Delta G (Gibbs free energy change) for a reaction is always positive when the reaction is non-spontaneous under the given conditions. This typically occurs when the system is at equilibrium or when the enthalpy change (ΔH) is positive and the entropy change (ΔS) is negative, leading to a situation where the temperature multiplied by ΔS (TΔS) is not sufficient to drive the reaction forward. Additionally, when the reactants are more stable than the products, or when the reaction requires external energy input to proceed, delta G will also be positive.
The spontaneity of a reaction is determined by the sign of the Gibbs free energy (ΔG). If both enthalpy (H) and entropy (S) are positive, the reaction can be spontaneous at high temperatures where the TΔS term outweighs the positive ΔH term, resulting in a negative ΔG. This means the reaction will be spontaneous at elevated temperatures.
Yes, a half-cell's standard reduction potential is positive if the reduction reaction is spontaneous under standard conditions.
A positive value of delta G (ΔG) indicates that a reaction is non-spontaneous under standard conditions, meaning it requires an input of energy to proceed. In this case, the products have higher free energy than the reactants, suggesting that the reaction is unfavorable in its current direction. Therefore, the reaction is more likely to occur when coupled with a spontaneous process or under different conditions that favor the formation of products.
The reaction will be spontaneous at high temperatures (T) where TΔS > ΔH, according to Gibbs free energy equation, ΔG = ΔH - TΔS. At high enough temperatures, the TΔS term can outweigh the positive ΔH term, leading to a negative ΔG value and a spontaneous reaction.
The direct product of the hydrolysis of an ester, under both acidic and basic conditions, is an alcohol and a carboxylic acid.
A positive value of G0 (standard Gibbs free energy change) indicates that the reaction is non-spontaneous under standard conditions. This means that, at standard temperature and pressure, the reactants are favored over the products, and the reaction will not proceed in the forward direction without the input of energy. In practical terms, it suggests that the reaction is thermodynamically unfavorable.
Argon is chemically inert and does not have any reaction under normal conditions.
A redox reaction with a positive standard electrode potential indicates that the reaction is spontaneous under standard conditions. This means that the tendency for the reduction half-reaction to occur is favored, making it more likely for the oxidizing agent to gain electrons. In practical terms, such reactions can drive processes like electrochemical cells, where energy is harnessed from the spontaneous electron transfer. Thus, a positive potential signifies a favorable thermodynamic outcome for the reaction.
A positive cell potential indicates that the redox reaction is spontaneous under standard conditions. This means that the reactants have a higher free energy than the products, leading to a favorable reaction that can occur without external energy input. Additionally, it suggests that the reduction half-reaction has a greater tendency to gain electrons compared to the oxidation half-reaction losing them.
That depends on the chemicals present before the chemical reaction and sometimes the conditions under which the chemical reaction occurred.