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2. The reaction shown below produces a mixture of 5 different products, some in fairly small amount. Write a complete reaction including any reactive intermediate(s) and draw each product. Label the rate-determining step and label the different reaction pathways with the type of mechanism involved. [Recall: -OTs is tosylate, a very good leaving group] "OTS CH3CH₂OH

2. The reaction shown below produces a mixture of 5 different products, some in fairly small amount. Write a complete reaction including any reactive intermediate(s) and draw each product. Label the rate-determining step and label the different reaction pathways with the type of mechanism involved. [Recall: -OTs is tosylate, a very good leaving group] "OTS CH3CH₂OH

Chemistry
Chemistry
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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
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after you write the five reacitons pathways, label the rate-determining step and mechanism please

2. The reaction shown below produces a mixture of 5 different products, some in fairly small amounts. Write a complete reaction including any reactive intermediate(s) and draw each product. Label the rate-determining step and label the different reaction pathways with the type of mechanism involved. [Recall: –OTs is tosylate, a very good leaving group] (Structure of cyclohexane with an –OTs group) CH₃CH₂OH --- In the diagram provided, the structure consists of a cyclohexane ring with a tosylate group (–OTs) attached. The arrow points to CH₃CH₂OH, suggesting that an ethanol molecule is involved in the reaction. **Key Points to Consider:** 1. **Tosylate as Leaving Group:** - Tosylate (–OTs) is highlighted as a very good leaving group, which plays a central role in the reaction mechanism. 2. **Reaction Mechanism Steps:** - Potential pathways include SN1, SN2, E1, or E2 reactions, dependent on the structure and conditions. - The rate-determining step is the slowest step in the reaction pathway, significantly affecting the reaction speed. 3. **Identifying Intermediates:** - Depending on the mechanism, possible intermediates such as carbocations may form, especially in SN1 or E1. 4. **Product Formation:** - The reaction results in five different products. Structures need to be drawn to identify each product correctly. 5. **Diagram Explanation:** - The diagram should include the structural changes from reactants to products, emphasizing different mechanistic pathways. This comprehensive analysis involves considering the reactivity of the tosylate group and the solvent influence due to ethanol, which may indicate nucleophilic substitution or elimination reactions.
Transcribed Image Text:2. The reaction shown below produces a mixture of 5 different products, some in fairly small amounts. Write a complete reaction including any reactive intermediate(s) and draw each product. Label the rate-determining step and label the different reaction pathways with the type of mechanism involved. [Recall: –OTs is tosylate, a very good leaving group] (Structure of cyclohexane with an –OTs group) CH₃CH₂OH --- In the diagram provided, the structure consists of a cyclohexane ring with a tosylate group (–OTs) attached. The arrow points to CH₃CH₂OH, suggesting that an ethanol molecule is involved in the reaction. **Key Points to Consider:** 1. **Tosylate as Leaving Group:** - Tosylate (–OTs) is highlighted as a very good leaving group, which plays a central role in the reaction mechanism. 2. **Reaction Mechanism Steps:** - Potential pathways include SN1, SN2, E1, or E2 reactions, dependent on the structure and conditions. - The rate-determining step is the slowest step in the reaction pathway, significantly affecting the reaction speed. 3. **Identifying Intermediates:** - Depending on the mechanism, possible intermediates such as carbocations may form, especially in SN1 or E1. 4. **Product Formation:** - The reaction results in five different products. Structures need to be drawn to identify each product correctly. 5. **Diagram Explanation:** - The diagram should include the structural changes from reactants to products, emphasizing different mechanistic pathways. This comprehensive analysis involves considering the reactivity of the tosylate group and the solvent influence due to ethanol, which may indicate nucleophilic substitution or elimination reactions.
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