Problem 51
Question
In the presence of peroxide, hydrogen chloride and hydrogen iodide do not undergo antiMarkownikoff's addition to alkenes because (a) both are highly ionic (b) one is oxidizing and the other is reducing (c) one of the steps is endothermic in both the cases (d) all the steps are exothermic in both the cases
Step-by-Step Solution
Verified Answer
The correct answer is (c) one of the steps is endothermic in both cases.
1Step 1: Understanding Anti-Markovnikov Addition
Anti-Markovnikov addition refers to the addition reaction where, contrary to Markovnikov's rule, the negative part of the adding molecule (e.g., halide ion) attaches to the less substituted carbon atom of the alkene. This reaction usually involves peroxide-initiated mechanism with the formation of radicals.
2Step 2: Analyzing Peroxide Effect
Peroxides can initiate radical reactions, such as the anti-Markovnikov addition. For alkenes to undergo this type of addition, the presence of a radical chain reaction mechanism is key, generally facilitated by peroxides and certain halogen acids, like HBr.
3Step 3: Applying to Hydrogen Chloride and Iodide
The anti-Markovnikov addition does not happen with HCl and HI even in the presence of peroxides. This could be explored by examining the energy changes in the steps of the radical mechanism.
4Step 4: Evaluating Energy Changes in Reaction Steps
For a radical-mediated reaction, some steps must fulfill specific thermodynamic criteria to proceed. An important aspect is that some of the radical intermediate formation steps are endothermic for both HCl and HI, meaning they absorb energy and are less favorable energetically, inhibiting the radical chain propagation.
Key Concepts
Radical Chain ReactionThermodynamics of ReactionsPeroxide EffectMarkovnikov's Rule
Radical Chain Reaction
A radical chain reaction is a process where radical intermediates are continuously reused to sustain the reaction. These reactions are commonly seen in organic chemistry, especially in mechanisms like anti-Markovnikov addition that involve radicals.
Here's how it works:
Here's how it works:
- Initiation: Radicals are generated, often using heat or light. For instance, in the presence of peroxides, alkanes can form radicals that start the chain reaction.
- Propagation: In this step, the radicals react with other molecules, turning these into additional radicals. This step is crucial because it continues the chain of reactions.
- Termination: The reaction concludes when radicals collide with each other, forming stable non-radical products.
Thermodynamics of Reactions
Thermodynamics is the study of heat and energy changes in a chemical reaction. For the radical chain reaction, specifically in anti-Markovnikov additions, understanding thermodynamics is essential as it impacts whether the reaction will proceed.
Consider the importance of energy changes in reactions:
Consider the importance of energy changes in reactions:
- Endothermic Reactions: These reactions absorb energy. They require an input of energy to proceed. For HCl and HI reacting in a radical chain, certain steps are endothermic, making the reaction less favorable.
- Exothermic Reactions: These release energy, often making them more likely to occur because they lead to a stable energy state. In radical chain reactions, steps that are exothermic help drive the propagation phase.
Peroxide Effect
The peroxide effect, also known as the Kharasch effect, is critical in facilitating radical reactions, including the anti-Markovnikov addition of alkenes.
Here's how peroxides come into play:
Here's how peroxides come into play:
- Peroxides decompose to form free radicals (typically at elevated temperatures) that initiate radical chain reactions.
- They break down to generate radicals capable of attacking alkenes to produce more radical species, a necessary condition for anti-Markovnikov additions.
Markovnikov's Rule
Markovnikov's Rule is a principle that guides the addition of compounds to alkenes. According to this rule, in a normal addition reaction, the hydrogen atom adds to the less substituted carbon atom, while the other component (e.g., halide ion) attaches to the more substituted carbon.
In contrast, anti-Markovnikov addition does not follow this rule. Instead, the incoming component adds to the less substituted carbon. The difference arises due to the mechanism:
In contrast, anti-Markovnikov addition does not follow this rule. Instead, the incoming component adds to the less substituted carbon. The difference arises due to the mechanism:
- Markovnikov: Typically involves ionic mechanisms where stability is paramount. The carbocation intermediate prefers more stable arrangements in accordance with Markovnikov's rule.
- Anti-Markovnikov: Initiated by radicals, relies on the presence of peroxides to form the less stable configurations not favored by ionic pathways.
Other exercises in this chapter
Problem 49
Which of the following undergoes nucleophillic substitution exclusively by \(\mathrm{SN}^{1}\) mechanism? (a) ethyl chloride (b) isopropyl chloride (c) chlorobe
View solution Problem 50
Which one of the following compounds is most acidic? (a) \(\mathrm{Cl}-\mathrm{CH}_{2}-\mathrm{CH}_{2}-\mathrm{OH}\) (b) Oc1ccccc1 (c) O=[N+]([O-])c1ccccc1O (d)
View solution Problem 54
The reaction intermediate in \(\mathrm{E}_{1 C b}\) is (a) Carbonium ion (b) carbon free radical (c) Carbanion (d) Carbene
View solution Problem 59
Which one of the following pairs is correctly matched? (a) Saytzeff rule, least substituted alkene (b) Hoffmann rule, most substituted alkene (c) \(\mathrm{E}_{
View solution