When the following reaction was run, the resulting organic products B and C were obtained. oft- 1% AgNO, EtOH B + C 'Br a) Write the mechanism for the transformation and identify the organic products B and C: b) The relationship between B and C is: a. Enantiomeric b. Diastereomeric C. Constitutional isomers d. The same compound e. None of the above C HE 850:50 C Et c) The mixture of B and C would give a specific rotation of [a] = 0° a. True b. False a carbor

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Chapter1: Chemical Foundations
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**HW2.**

When the following reaction was run, the resulting *organic* products B and C were obtained.

(Reaction scheme showing a brominated cyclohexane derivative reacting with 1% AgNO₃ and EtOH to form products B and C)

**a)** Write the mechanism for the transformation and identify the organic products B and C:

---

**b)** The relationship between B and C is:
- a. Enantiomeric
- b. Diastereomeric
- c. Constitutional isomers
- d. The same compound
- e. None of the above

---

**c)** The mixture of B and C would give a specific rotation of \([α]_{D}^{25} = 0°\)
- a. True
- b. False
Transcribed Image Text:**HW2.** When the following reaction was run, the resulting *organic* products B and C were obtained. (Reaction scheme showing a brominated cyclohexane derivative reacting with 1% AgNO₃ and EtOH to form products B and C) **a)** Write the mechanism for the transformation and identify the organic products B and C: --- **b)** The relationship between B and C is: - a. Enantiomeric - b. Diastereomeric - c. Constitutional isomers - d. The same compound - e. None of the above --- **c)** The mixture of B and C would give a specific rotation of \([α]_{D}^{25} = 0°\) - a. True - b. False
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