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Consider the following energy diagram for the conversion of A→G.

a. Which points on the graph correspond to transition states?

b. Which points on the graph correspond to reactive intermediates?

c. How many steps are present in the reaction mechanism?

d. Label each step of the mechanism as endothermic or exothermic.

e. Label the overall reaction as endothermic or exothermic.

Short Answer

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Answer

  1. Points B, D, and F are the transition states.
  2. Points C and E are the reactive intermediates.
  3. The reaction has three steps.
  4. Step A-C is endothermic. While the steps C-E and E-G are exothermic.
  5. The overall reaction is exothermic.

Step by step solution

01

Step-by-Step SolutionStep 1: Transition States

Transition State is a higher energy partial molecular state. The energy of the transition state is the minimum threshold energy that is required for the conversion of reactants to the products in concerted reactions.

The transition state cannot be isolated from the reaction medium.

02

Intermediates

The intermediates are highly unstable molecules that form in between the reaction pathway.

The intermediates can be isolated from the reaction mixture.

03

Explanation

  1. Points B, D, and F are the transition states.
  2. Points C and E are the reactive intermediates.
  3. Since the reaction has three transition states, the reaction has three steps.
  4. In step A-C, the energy of the intermediate C is higher. Hence, the reaction is endothermic. In steps C-E and E-G, the energy of the intermediates C and E are higher. Hence, the reactions in these steps are exothermic.
  5. The overall reaction is exothermic.

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Most popular questions from this chapter

a. Which value corresponds to a negative value of ∆G°:Keq=10-2or Keq=102?

b. In a unimolecular reaction with five times as much starting material as product at equilibrium, what is the value of Keq? Is ∆G°positive or negative?

c. Which value corresponds to a larger Keq: ∆G°=-8kJ/molor ∆G°=20kJ/mol?

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.

Given each of the following values, is the starting material or product favored at equilibrium?

a.Keq=5.5

b.Δ³Ò°=40kJ/mol


Consider the following energy diagram

  1. How many steps are involved in this reaction?
  2. Label ∆H°and Ea for each step, and label∆H°overall .
  3. Label each transition state.
  4. Which point on the graph corresponds to a reactive intermediate?
  5. Which step is rate-determining?
  6. Is the overall reaction endothermic or exothermic?

What carbon radical is formed by homolysis of theC-Ha bond in propylbenzene? Draw all reasonable resonance structures for this radical.

What carbon radical is formed by homolysis of therole="math" localid="1648540916945" C-Hbbond in propylbenzene? Draw all reasonable resonance structures for this radical.

The bond dissociation energy of one of the C-H bonds is considerably less than the bond dissociation energy of the other. Which C-H bond is weaker? Offer an explanation.

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