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 freeConsider the following energy diagram for the conversion of .
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.
For a reaction with and , decide which of the following statements is (are) true. Correct any false statement to make it true. Ignore entropy considerations. (a) The reaction is faster than a reaction with and . (b) The reaction is faster than a reaction with and . (c) for the reaction is a positive value. (d) The starting materials are lower in energy than the products of the reaction. (e) The reaction is exothermic.
Draw the transition state for each reaction.
a.
b.
The conversion of acetyl chloride to methyl acetate occurs via the following two-step mechanism:
a. Add curved arrows to show the movement of the electrons in each step.
b. Write the rate equation for this reaction, assuming the first step is rate-determining.
c. If the concentration of were increased 10 times, what would happen to the rate of the reaction?
d. If the concentrations of both and were increased 10 times, what would happen to the rate of the reaction?
e. Classify the conversion of acetyl chloride to methyl acetate as an addition, elimination, or substitution.
Esterification is the reaction of a carboxylic acid (RCOOH) with an alcohol (R'OH) to form an ester (RCOOR') with a loss of water. Equation [1] is an example of an intermolecular esterification reaction. Equation [2] is an example of an intramolecular esterification reaction; that is, the carboxylic acid and alcohol are contained in the same starting material, forming a cyclic ester as the product. The equilibrium constants for both reactions are given. Explain why is different for these two apparently similar reactions.
[1]
[2]
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