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For which of the following reactions is S°a positive value?

a.

b.

Short Answer

Expert verified

Answer

  1. S°is positive.
  2. No change in S°.

Step by step solution

01

Step-by-Step SolutionStep 1: Entropy Change

The entropy change is the change in the randomness of the system when the reactants undergo a reaction to form products.

Conventionally, the value of entropy S°should be higher for products.

02

Comparison of Entropy for reactants and products

When two reactants combine to form a single product, the disorderliness decreases. Hence, the entropy of the system decreases in going from reactants to products.

When a single reactant dissociates to form two or more products, the randomness in the products increases, hence, the entropy of the products increases, and that is favored.

03

Explanation

  1. Since the number of molecules in the products is more than the number of molecules of reactants the entropy of the products is more. Hence, S°is positive.
  2. The number of molecules of reactants and products is the same. Hence, there is no change in the entropy of the system. So, neither of the products or the reactants are favored.

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Most popular questions from this chapter

As we will learn in Section 15.12, many antioxidants—compounds that prevent unwanted radical oxidation reactions from occurring—are phenols, compounds that contain an OH group bonded directly to a benzene ring.

  1. Explain why homolysis of the O-H bond in phenol requires considerably less energy than homolysis of the O-H bond in ethanol (362 kJ/mol vs 438 kJ/mol).
  2. Why is the C-O bond in phenol shorter than C-O bond in ethanol?

By taking into account electronegativity differences, draw the products formed by heterolysis of the carbon-heteroatom bond in each molecule. Classify the organic reactive intermediate as a carbocation or a carbanion.

The conversion of (CH3)3Clto (CH3)2C=CH2can occur by either a one-step or a two-step mechanism, as shown in Equations [1] and [2].

a. What rate equation would be observed for the mechanism in Equation [1]?

b. What rate equation would be observed for the mechanism in Equation [2]?

c. What is the order of each rate equation (i.e., first, second, and so forth)?

d. How can these rate equations be used to show which mechanism is the right one for this reaction?

e. Assume Equation [1] represents an endothermic reaction and draw an energy diagram for the reaction. Label the axes, reactants, products, Ea, and H°. Draw the structure for the transition state.

f. Assume Equation [2] represents an endothermic reaction and that the product of the rate-determining step is higher in energy than the reactants or products. Draw an energy diagram for this two-step reaction. Label the axes, reactants and products for each step, and the Eaand H°for each step. Label H°overall. Draw the structure for both transition states.

Rank the indicated bonds in order of increasing bond dissociation energy.

PGF2α (Section 4.15) is synthesized in cells using a cyclooxygenase enzyme that catalyzesa multistep radical pathway. Two steps in the pathway are depicted in the accompanying equations.

(a) Draw in curved arrows to illustrate how C is converted to D in Step [1].

(b) Identify Y, the product of Step [2], using the curved arrows that are drawn on compound D.

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