Using the reagents below, list in order (by letter, no period) those necessary to prepare the product of the following reaction scheme. Note: Not all spaces provided may be needed. Type "na" in any space where you have no reagent. a. Br₂, heat, light b. Br2, dark NaBH OH

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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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This image presents a chemical reaction scheme aimed at transforming cyclohexane into an epoxide structure. Below the reaction scheme, reagents are listed for selection in the synthesis steps. The task is to select the correct order of reagents to achieve the final product.

**Reagents:**
- a. Br₂, heat, light
- b. Br₂, dark
- c. NaBH₄, OH⁻
- d. BH₃:THF
- e. NaOEt, EtOH
- f. H₂O₂, OH⁻
- g. Br₂, H₂O

**Steps to Product:**
1. **Step #1 (a):** Use Br₂ with heat and light to initiate a free radical bromination on cyclohexane, producing bromo-cyclohexane.
2. **Step #2 (e):** Apply NaOEt in ethanol (EtOH) to perform elimination, resulting in the formation of a cyclohexene.
3. **Step #3 (g):** Use Br₂ in water (H₂O) to form a bromohydrin from the cyclohexene.
4. **Step #4:** (Not listed; relevant only to available choices).

The reaction progresses from an alkane to a bromoalkane, followed by an alkene, and finally an epoxide via various chemical transformations.
Transcribed Image Text:This image presents a chemical reaction scheme aimed at transforming cyclohexane into an epoxide structure. Below the reaction scheme, reagents are listed for selection in the synthesis steps. The task is to select the correct order of reagents to achieve the final product. **Reagents:** - a. Br₂, heat, light - b. Br₂, dark - c. NaBH₄, OH⁻ - d. BH₃:THF - e. NaOEt, EtOH - f. H₂O₂, OH⁻ - g. Br₂, H₂O **Steps to Product:** 1. **Step #1 (a):** Use Br₂ with heat and light to initiate a free radical bromination on cyclohexane, producing bromo-cyclohexane. 2. **Step #2 (e):** Apply NaOEt in ethanol (EtOH) to perform elimination, resulting in the formation of a cyclohexene. 3. **Step #3 (g):** Use Br₂ in water (H₂O) to form a bromohydrin from the cyclohexene. 4. **Step #4:** (Not listed; relevant only to available choices). The reaction progresses from an alkane to a bromoalkane, followed by an alkene, and finally an epoxide via various chemical transformations.
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