Deuterium (D) is the hydrogen isotope of mass number 2, with a proton and a neutron in its nucleus. The chemistry of deuterium is nearly identical to the chemistry of hydrogen, except that the C―D bond is slightly stronger than the C―H bond by 5.0 kJ/mol (1.2 kcal/mol). Reaction rates tend to be slower when a C―D bond (as opposed to a C―H bond) is broken in a rate-limiting step.This effect, called a kinetic isotope effect, is clearly seen in the chlorination of methane. Methane undergoes free-radical chlorination 12 times as fast as tetradeuteriomethane (CD4)Faster: CH4 + Cl⋅ —> CH3Cl + HCl relative rate= 12Slower: CD4 + Cl⋅ —> CD3Cl + DClrelative rate= 1 c. Consider the thermodynamics of the chlorination of methane and the chlorination of ethane, and use the Hammond postulate to explain why one of these reactions has a much larger isotope effect than the other.

Using the bond-dissociation energies in Table 5.6,

(b) Will the transition state be reactant-like or product-like? Explain your answer.

Which of the following statements about the Hammond postulate is not true?

According to the Hammond postulate, the transition state of an $\mathrm{endo}-\mathrm{thermic}$ reaction will resemble which of the following?

Deuterium (D) is the hydrogen isotope of mass number 2, with a proton and a neutron in its nucleus. The chemistry of deuterium is nearly identical to the chemistry of hydrogen, except that the C―D bond is slightly stronger than the C―H bond by 5.0 kJ/mol (1.2 kcal/ mol). Reaction rates tend to be slower when a C―D bond (as opposed to a C―H bond) is broken in a rate-limiting step.

This effect, called a kinetic isotope effect, is clearly seen in the chlorination of methane. Methane undergoes free-radical chlorination 12 times as fast as tetradeuteriomethane (CD₄).

c. Consider the thermodynamics of the chlorination of methane and the chlorination of ethane, and use the Hammond postulate to explain why one of these reactions has a much larger isotope effect than the other.

In the presence of a small amount of bromine, cyclohexene undergoes the following light-promoted reaction:

b. Draw the structure of the rate-limiting transition state.

c. Use Hammond's postulate to predict which intermediate most closely resembles this transition state.

Assuming that ∆H° = -15kcal/mol for the reaction in Assessment 5.31(b), show the transition state for the forward and reverse reactions.

For each of the following acid–base reactions, (iv) draw the transition state, paying close attention to the degree of bond forming and breaking present in the transition state. If a pK_a is not one of the ten common ones we learned in Chapter 4, it will be given to you.

(a)