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Place the best reagent in the bin for each of these reactions involving cyclohexylmethanol. Br Answer Bank NaBr NaH PCC CrO, , H¸O* SOI, HBr CH, I PBr. HO, HO. HCI MCPBA H, SO, NaCl

Place the best reagent in the bin for each of these reactions involving cyclohexylmethanol. Br Answer Bank NaBr NaH PCC CrO, , H¸O* SOI, HBr CH, I PBr. HO, HO. HCI MCPBA H, SO, NaCl

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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**Title: Selection of Reagents for Reactions Involving Cyclohexylmethanol** **Introduction:** This activity requires the identification of the most appropriate reagent for each of the given reactions involving cyclohexylmethanol. The goal is to transform the starting materials into specific products using the reagents from the provided answer bank. **Reaction Pathways:** 1. **Bromination Reaction:** - Starting Material: Cyclohexylmethanol - Product: Cyclohexylmethanol with a bromine atom - **Reagent Box:** Choose from the answer bank to substitute the OH group with a Br. 2. **Oxidation Reaction:** - Starting Material: Cyclohexylmethanol - Product: Cyclohexanecarboxylic acid - **Reagent Box:** Select the appropriate reagent to oxidize the alcohol to a carboxylic acid. 3. **Conversion to Chloride:** - Starting Material: Cyclohexylmethanol - Product: Cyclohexylmethanol with a chlorine atom - **Reagent Box:** Pick the reagent that will replace the OH group with Cl. 4. **Epoxidation or Oxidation:** - Starting Material: Cyclohexylmethanol - Product: A compound with an oxidized feature (possibly ketone or aldehyde) - **Reagent Box:** Determine the correct oxidizing agent for this transformation. 5. **Ester Formation:** - **Pathway 1:** - Starting Material: Cyclohexylmethanol - Intermediate: An alkoxide ion - **Reagent Box 1:** Choose the reagent to deprotonate the alcohol. - **Pathway 2:** - Intermediate: Alkokide ion reacting to form the final ester - **Reagent Box 2:** Choose the alkylating agent to form the ester. **Answer Bank:** - NaBr - NaH - PCC - CrO₃, H₃O⁺ - SOCl₂ - HBr - CH₃I - PBr₃ - HCl - mCPBA - H₂SO₄ - NaCl **Conclusion:** Use the answer bank to fill in the blanks with the most suitable reagents for each
Transcribed Image Text:**Title: Selection of Reagents for Reactions Involving Cyclohexylmethanol** **Introduction:** This activity requires the identification of the most appropriate reagent for each of the given reactions involving cyclohexylmethanol. The goal is to transform the starting materials into specific products using the reagents from the provided answer bank. **Reaction Pathways:** 1. **Bromination Reaction:** - Starting Material: Cyclohexylmethanol - Product: Cyclohexylmethanol with a bromine atom - **Reagent Box:** Choose from the answer bank to substitute the OH group with a Br. 2. **Oxidation Reaction:** - Starting Material: Cyclohexylmethanol - Product: Cyclohexanecarboxylic acid - **Reagent Box:** Select the appropriate reagent to oxidize the alcohol to a carboxylic acid. 3. **Conversion to Chloride:** - Starting Material: Cyclohexylmethanol - Product: Cyclohexylmethanol with a chlorine atom - **Reagent Box:** Pick the reagent that will replace the OH group with Cl. 4. **Epoxidation or Oxidation:** - Starting Material: Cyclohexylmethanol - Product: A compound with an oxidized feature (possibly ketone or aldehyde) - **Reagent Box:** Determine the correct oxidizing agent for this transformation. 5. **Ester Formation:** - **Pathway 1:** - Starting Material: Cyclohexylmethanol - Intermediate: An alkoxide ion - **Reagent Box 1:** Choose the reagent to deprotonate the alcohol. - **Pathway 2:** - Intermediate: Alkokide ion reacting to form the final ester - **Reagent Box 2:** Choose the alkylating agent to form the ester. **Answer Bank:** - NaBr - NaH - PCC - CrO₃, H₃O⁺ - SOCl₂ - HBr - CH₃I - PBr₃ - HCl - mCPBA - H₂SO₄ - NaCl **Conclusion:** Use the answer bank to fill in the blanks with the most suitable reagents for each
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