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

a.

b.

Short Answer

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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

Homolysis of the indicated C-H bond in propene forms a resonance-stabilized radical.

  1. Draw the two possible resonance structures for this radical.
  2. Use half-headed curved arrows to illustrate how one resonance structure can be converted to the other.
  3. Draw a structure for the resonance hybrid.

Calculate ΔH° for each oxidation reaction. Each equation is balanced as written; remember to take into account the coefficients in determining the number of bonds broken or formed.

[ ΔHfor O2=497kJ/mol ; ΔHfor one C=O in CO2=535kJ/mol]

a.role="math" localid="1648191068323" CH4+2O2CO2+2H2O

b.2CH4+7O24CO2+6H2O


Question: Classify the conversion of A to B as a substitution, elimination, or addition. B can be converted to the female sex hormone estrone in two steps.

Consider the following two-step reaction:

a. How many bonds are broken and formed in Step [1]? Would you predict H°of Step [1] to be positive or negative?

b. How many bonds are broken and formed in Step [2]? Would you predict the H°of Step [2] to be positive or negative?

c. Which step is rate-determining?

d. Draw the structure for the transition state in both steps of the mechanism.

e. If H°overallis negative for this two-step reaction, draw an energy diagram illustrating all of the information in parts (a)–(d).

Consider the following energy diagram

  1. How many steps are involved in this reaction?
  2. Label H°and Ea for each step, and labelH°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?
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