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2. -CH3 1. OH 2. + H3C-Mgl a Proton transfer b = Lewis acid/base c = Electrophilic addition aqueous H₂SO4 dry ether OH хоно Mgl + d = E1 Elimination e E2 Elimination CH₂ The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. f = SN1 Nucleophilic substitution gSN2 Nucleophilic substitution

2. -CH3 1. OH 2. + H3C-Mgl a Proton transfer b = Lewis acid/base c = Electrophilic addition aqueous H₂SO4 dry ether OH хоно Mgl + d = E1 Elimination e E2 Elimination CH₂ The rections above involve synthesis or reactions of alcohols and ethers. Identify the mechanism by which they proceed from among the mechanisms listed. Use the letters a - g for your answers. f = SN1 Nucleophilic substitution gSN2 Nucleophilic substitution

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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## Educational Resource on Reaction Mechanisms ### Reaction Schemes #### 1. The first reaction depicts a Grignard reaction: - A phenylmethyl alcohol reacts with methyl magnesium iodide in dry ether to produce a phenyl methyl ketone, magnesium iodide (MgI), and methane (CH₄). #### 2. The second reaction shows an acid-catalyzed etherification: - Cyclohexanol reacts in aqueous H₂SO₄ to form cyclohexene. ### Mechanism Key - **a** = Proton transfer - **b** = Lewis acid/base - **c** = Electrophilic addition - **d** = E1 Elimination - **e** = E2 Elimination - **f** = S<sub>N</sub>1 Nucleophilic substitution - **g** = S<sub>N</sub>2 Nucleophilic substitution ### Instructions The reactions above illustrate the synthesis or reactions of alcohols and ethers. Identify which reaction mechanism each transformation proceeds through using the letters **a - g**. **1.** [Write your answer here] **2.** [Write your answer here]
Transcribed Image Text:## Educational Resource on Reaction Mechanisms ### Reaction Schemes #### 1. The first reaction depicts a Grignard reaction: - A phenylmethyl alcohol reacts with methyl magnesium iodide in dry ether to produce a phenyl methyl ketone, magnesium iodide (MgI), and methane (CH₄). #### 2. The second reaction shows an acid-catalyzed etherification: - Cyclohexanol reacts in aqueous H₂SO₄ to form cyclohexene. ### Mechanism Key - **a** = Proton transfer - **b** = Lewis acid/base - **c** = Electrophilic addition - **d** = E1 Elimination - **e** = E2 Elimination - **f** = S<sub>N</sub>1 Nucleophilic substitution - **g** = S<sub>N</sub>2 Nucleophilic substitution ### Instructions The reactions above illustrate the synthesis or reactions of alcohols and ethers. Identify which reaction mechanism each transformation proceeds through using the letters **a - g**. **1.** [Write your answer here] **2.** [Write your answer here]
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