Domanda del libro di testo
For each compound, predict the major product of free-radical bromination. Remember that bromination is highly selective, and only the most stable radical will be formed.
(e)
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Ch.4 - The Study of Chemical Reactions
Wade9th EditionOrganic ChemistryISBN: 9780135213728
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TOC.tableOfContents
- Ch.1 - Structure and Bonding107
- Ch. 2 - Acids and Bases; Functional Groups115
- Ch.3 - Structure and Stereochemistry of Alkanes100
- Ch.4 - The Study of Chemical Reactions99
- Ch.5 - Stereochemistry93
- Ch.6 - Alkyl Halides; Nucleophilic Substitution118
- Ch. 7 - Structure and Synthesis of Alkenes; Elimination158
- Ch.8 - Reactions of Alkenes171
- Ch.9 - Alkynes91
- Ch.10 - Structure and Synthesis of Alcohols143
- Ch.11 - Reactions of Alcohols104
- Ch. 12 - Infrared Spectroscopy and Mass Spectrometry22
- Ch. 13 - Nuclear Magnetic Resonance Spectroscopy45
- Ch. 14 - Ethers, Epoxides, and Thioethers72
- Ch. 15 - Conjugated Systems, Orbital Symmetry, and Ultraviolet Spectroscopy89
- Ch. 16 - Aromatic Compounds74
- Ch. 17 - Reactions of Aromatic Compounds126
- Ch. 18 - Ketones and Aldehydes193
- Ch. 19 - Amines129
- Ch. 20 - Carboxylic Acids77
- Ch. 21 - Carboxylic Acid Derivatives141
- Ch. 22 - Condensations and Alpha Substitutions of Carbonyl Compounds175
- Ch. 23 - Carbohydrates and Nucleic Acids93
- Ch. 24 - Amino Acids, Peptides, and Proteins54
Capitolo 4, Problema 48a
When exactly 1 mole of methane is mixed with exactly 1 mole of chlorine and light is shone on the mixture, a chlorination reaction occurs. The products are found to contain substantial amounts of di-, tri-, and tetrachloromethane, as well as unreacted methane.
a. Explain how a mixture is formed from this stoichiometric mixture of reactants, and propose mechanisms for the formation of these compounds from chloromethane.
Guida verificata passo dopo passo1
Understand the reaction: The reaction between methane (CH₄) and chlorine (Cl₂) in the presence of light is a free radical substitution reaction. The light provides energy to break the Cl-Cl bond, initiating the reaction. This process is called photochemical chlorination.
Step 1: Initiation - The Cl₂ molecule absorbs light energy, causing homolytic cleavage of the Cl-Cl bond to form two chlorine radicals (Cl•). This can be represented as: Cl₂ → 2Cl•.
Step 2: Propagation - The chlorine radical reacts with methane (CH₄), abstracting a hydrogen atom to form hydrochloric acid (HCl) and a methyl radical (CH₃•). This is followed by the methyl radical reacting with another Cl₂ molecule to form chloromethane (CH₃Cl) and another chlorine radical. These steps can be written as: Cl• + CH₄ → CH₃• + HCl and CH₃• + Cl₂ → CH₃Cl + Cl•.
Step 3: Formation of higher chlorinated products - The chloromethane (CH₃Cl) formed in the propagation step can undergo further substitution reactions. The chlorine radical can abstract another hydrogen atom from CH₃Cl to form dichloromethane (CH₂Cl₂), and this process can continue to form trichloromethane (CHCl₃) and tetrachloromethane (CCl₄). Each step involves the same propagation mechanism: Cl• + CH₃Cl → CH₂Cl• + HCl, CH₂Cl• + Cl₂ → CH₂Cl₂ + Cl•, and so on.
Step 4: Termination - The reaction can terminate when two radicals combine to form a stable molecule, such as Cl• + Cl• → Cl₂ or CH₃• + Cl• → CH₃Cl. These termination steps reduce the number of radicals in the system, slowing down the reaction. The mixture of products (CH₄, CH₃Cl, CH₂Cl₂, CHCl₃, and CCl₄) arises because the reaction does not stop after the formation of CH₃Cl, and further substitutions occur due to the presence of excess chlorine radicals.
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Stoichiometry
Stoichiometry is the calculation of reactants and products in chemical reactions based on the conservation of mass. In this context, it refers to the precise mixing of 1 mole of methane and 1 mole of chlorine, which allows for the prediction of the amounts of products formed. Understanding stoichiometry is essential for analyzing how reactants interact and the ratios in which they combine to form various chlorinated methane products.
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Free Radical Mechanism
The chlorination of methane occurs via a free radical mechanism, which involves the formation of reactive intermediates called free radicals. When light is shone on the mixture, it initiates the reaction by breaking the Cl-Cl bond, generating chlorine radicals. These radicals then react with methane to form chloromethane and further react to produce di-, tri-, and tetrachloromethane through successive substitution reactions.
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Substitution Reactions
Substitution reactions involve the replacement of one atom or group in a molecule with another atom or group. In the case of chlorination, chlorine atoms replace hydrogen atoms in methane, leading to the formation of chlorinated products. The reaction can proceed through multiple steps, resulting in various chlorinated compounds, such as dichloromethane, trichloromethane, and tetrachloromethane, depending on the number of substitutions that occur.
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b. Predict the ratios in which these monochlorination products will be formed, remembering that a chlorine atom abstracts a secondary hydrogen about 4.5 times as fast as it abstracts a primary hydrogen.
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Domanda del libro di testo
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The chlorination of pentane gives a mixture of three monochlorinated products.
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For each compound, predict the major product of free-radical bromination. Remember that bromination is highly selective, and only the most stable radical will be formed.
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Domanda del libro di testo
When exactly 1 mole of methane is mixed with exactly 1 mole of chlorine and light is shone on the mixture, a chlorination reaction occurs. The products are found to contain substantial amounts of di-, tri-, and tetrachloromethane, as well as unreacted methane.
b. How would you run this reaction to get a good conversion of methane to CH3Cl? Of methane to CCl4?
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