Chapter 6: Problem 6.6 (page 223)
Which bond in each pair has the higher bond dissociation energy?
a.
b.
Short Answer
a.
b.
Chapter 6: Problem 6.6 (page 223)
Which bond in each pair has the higher bond dissociation energy?
a.
b.
a.
b.
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Get started for freea. Which corresponds to a negative value of localid="1648198317845" , localid="1648198334107" or Keq= 0.001 ?
b. Which corresponds to a lower value oflocalid="1648198364090" , localid="1648198396853" or localid="1648198411007" ?
Indicate which factors affect the rate of a reaction.
Calculate ΔH° for each reaction.
The Diels–Alder reaction, a powerful reaction discussed in Chapter 16, occurs when a 1,3- diene such as A reacts with an alkene such as B to form the six-membered ring in C.
a. Draw curved arrows to show how A and B react to form C.
b. What bonds are broken and formed in this reaction?
c. Would you expect this reaction to be endothermic or exothermic?
d. Does entropy favor the reactants or products?
e. Is the Diels–Alder reaction a substitution, elimination, or addition?
The conversion of to can 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, , and . 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 and for each step. Label overall. Draw the structure for both transition states.
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