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1. Which of the following is not expected to be intermediate of the following reaction ? OH H2O (а) (b) (c) (d)

1. Which of the following is not expected to be intermediate of the following reaction ? OH H2O (а) (b) (c) (d)

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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**Question 1:** **Which of the following is not expected to be an intermediate of the following reaction?** The reaction is given as: \[ \text{Cyclohexyl iodide} \xrightarrow{\text{H}_2\text{O}} \text{Cyclohexanol} \] Options for intermediates: - (a) Cyclohexyl cation - (b) Cyclohexyl cation with a secondary carbocation indicated by a positive charge at the secondary carbon - (c) Cyclohexanol with a water molecule and a positive charge on the oxygen, indicating a protonated form - (d) Cyclohexyl cation with a positive charge indicated elsewhere **Explanation of Diagrams:** - The initial reactant shows cyclohexane with an iodide group attached. The reaction involves water as a reagent to convert this into cyclohexanol. - Four possible intermediates are shown as cyclohexane rings with positive charges on different atoms, indicating carbocations or protonated species.
Transcribed Image Text:**Question 1:** **Which of the following is not expected to be an intermediate of the following reaction?** The reaction is given as: \[ \text{Cyclohexyl iodide} \xrightarrow{\text{H}_2\text{O}} \text{Cyclohexanol} \] Options for intermediates: - (a) Cyclohexyl cation - (b) Cyclohexyl cation with a secondary carbocation indicated by a positive charge at the secondary carbon - (c) Cyclohexanol with a water molecule and a positive charge on the oxygen, indicating a protonated form - (d) Cyclohexyl cation with a positive charge indicated elsewhere **Explanation of Diagrams:** - The initial reactant shows cyclohexane with an iodide group attached. The reaction involves water as a reagent to convert this into cyclohexanol. - Four possible intermediates are shown as cyclohexane rings with positive charges on different atoms, indicating carbocations or protonated species.
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