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Which bond in each pair has the higher bond dissociation energy?

a.

b.

Short Answer

Expert verified

a.

b.

Step by step solution

01

Step-by-Step SolutionStep 1: Bond dissociation energy

The amount of energy that is essential to break a chemical bond is termed the bond dissociation energy.

02

Factors affecting bond dissociation energy

Size of the bonded atoms: As the size of the bonded atom increases the bond length increases and the bond strength decreases thereby decreasing the bond dissociation energy.

The number of electrons involved in bonding: As the number of electrons shared between two atoms (i.e., the number of bonds between two atoms) increases the bond strength increases and thus the bond dissociation energy also increases.

03

Bonds with high bond dissociation energy

a.

The compound with higher bond dissociation energy

The first compound consists of a carbon-oxygen (C-O) and the second compound consists of a carbon-sulfur (C-S) bond.

Since sulfur is bigger in size than oxygen the carbon-sulfur (C-S) bond is weaker compared to the carbon-oxygen (C-O) bond.

Therefore, the carbon-oxygen (C-O) bond has higher bond dissociation energy than the carbon-sulfur (C-S) bond.

b.

Compound with higher bond dissociation energy

The first compound consists of a carbon-oxygen double bond while the second one has a carbon-oxygen single bond.

Since a double bond has higher bond strength than a single bond, the carbon-oxygen double bond (C=O) has higher bond dissociation energy than the carbon-oxygen single bond (C-O).

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Most popular questions from this chapter

Consider the following energy diagram for the conversion of Aโ†’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.

For a reaction with Keq=0.8and Ea=80kJ/mol, 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 Keq=8and Ea=80kJ/mol. (b) The reaction is faster than a reaction with Keq=0.8and Ea=40kJ/mol. (c) โˆ†Gยฐ 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 Keqis different for these two apparently similar reactions.

[1]

[2]

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