**Synthesis Problem:****Instructions:** Place reagents in each box below that would produce each product shown in the highest yield.**Diagram Details:**1. **Reaction 1:** - **Starting Material:** Cyclohexanol (indicated by the hexagonal ring with an -OH group attached). - **Product:** Cyclohexyl tosylate (indicated by the hexagonal ring with an -OTs group attached). - **Box:** Insert the reagent(s) needed to convert cyclohexanol to cyclohexyl tosylate.2. **Reaction 2:** - **Starting Material:** Cyclohexyl tosylate (indicated by the hexagonal ring with an -OTs group). - **Product:** Cyclohexene (indicated by the hexagonal ring with a double bond). - **Box:** Insert the reagent(s) needed to convert cyclohexyl tosylate to cyclohexene.3. **Reaction 3:** - **Starting Material:** Cyclohexene (indicated by the hexagonal ring with a double bond). - **Product:** Bromocyclohexane (indicated by the hexagonal ring with a -Br group attached). - **Box:** Insert the reagent(s) needed to convert cyclohexene to bromocyclohexane.These transformations illustrate common reactions in organic synthesis, such as the conversion of alcohols to tosylates, elimination reactions to form alkenes, and halogenation of alkenes to form alkyl halides.

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Answered: 3. Synthesis: Place reagents in each…

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3. Synthesis: Place reagents in each box below that would produce each product shown in the highest yield. OH OTS Br

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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Concept explainers

Alkynes

Alkynes are organic compounds that contain at least one triple bond between carbon-carbon atoms. They are a series of unsaturated compounds with a general molecular formula, CnH2n-2.

Question

**Synthesis Problem:**

**Instructions:** Place reagents in each box below that would produce each product shown in the highest yield.

**Diagram Details:**

1. **Reaction 1:**
- **Starting Material:** Cyclohexanol (indicated by the hexagonal ring with an -OH group attached).
- **Product:** Cyclohexyl tosylate (indicated by the hexagonal ring with an -OTs group attached).
- **Box:** Insert the reagent(s) needed to convert cyclohexanol to cyclohexyl tosylate.

2. **Reaction 2:**
- **Starting Material:** Cyclohexyl tosylate (indicated by the hexagonal ring with an -OTs group).
- **Product:** Cyclohexene (indicated by the hexagonal ring with a double bond).
- **Box:** Insert the reagent(s) needed to convert cyclohexyl tosylate to cyclohexene.

3. **Reaction 3:**
- **Starting Material:** Cyclohexene (indicated by the hexagonal ring with a double bond).
- **Product:** Bromocyclohexane (indicated by the hexagonal ring with a -Br group attached).
- **Box:** Insert the reagent(s) needed to convert cyclohexene to bromocyclohexane.

These transformations illustrate common reactions in organic synthesis, such as the conversion of alcohols to tosylates, elimination reactions to form alkenes, and halogenation of alkenes to form alkyl halides.

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