12. Draw the products of the following reactions. Indicate stereochemistry when relevant. a CH-C = CH-Cs-CH D03, 2)Zn, H3 o %3D Brz C) 1) Bits, THE 2)402, OH

Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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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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The document appears to be a page from a chemistry notebook or textbook focusing on organic reactions. Below is a transcription suitable for an educational website:

---

**Exercise 12: Draw the products of the following reactions. Indicate stereochemistry when relevant.**

**a)**  
Reaction: \( \text{CH}_3 - \text{C} = \text{CH - CH}_2 - \text{CH}_3 \)  
Reagents:  
1) \( \text{O}_3 \)  
2) \( \text{Zn, H}_3\text{O}^+ \)

**b)**  
Structure: Cyclohexene  
Reagent: \( \text{Br}_2, \text{CCl}_4 \)

**c)**  
Structure: Cyclohexene  
Reagents:  
1) \( \text{BH}_3, \text{THF} \)  
2) \( \text{H}_2\text{O}_2, \text{OH}^- \)

**d)**  
Structure: Cyclohexene  
Reagent: \( \text{NBS} \)  
Solvent: \( \text{H}_2\text{O, DMSO} \)

**e)**  
Structure: Cyclohexene  
Reagents:  
1) \( \text{Hg(OAc)}_2, \text{H}_2\text{O} \)  
2) \( \text{NaBH}_4 \)

**f)**  
Reaction: Cyclohexene + \( \text{CF}_3\text{CO}_3\text{H} \)  
(Product structure not shown)

**g)**  
Structure: Cyclohexene  
Reagent: \( \text{H}_2/\text{Pd} \)

**h)**  
Reaction:  
\[ 
\begin{array}{l}
\ \ \ \ \ \ \ \ \ \text{H} \\
\ \ \ \text{f. } \\
\text{H}_3\text{C} - \text{C} - \text{H} \\
\ \ \ \text{H}_3\text{C} \\
\end{array}
\]
Reagent: \( \text{KMnO}_4, \text{H}_3\text{O}^+ \)

---

This transcription should
Transcribed Image Text:The document appears to be a page from a chemistry notebook or textbook focusing on organic reactions. Below is a transcription suitable for an educational website: --- **Exercise 12: Draw the products of the following reactions. Indicate stereochemistry when relevant.** **a)** Reaction: \( \text{CH}_3 - \text{C} = \text{CH - CH}_2 - \text{CH}_3 \) Reagents: 1) \( \text{O}_3 \) 2) \( \text{Zn, H}_3\text{O}^+ \) **b)** Structure: Cyclohexene Reagent: \( \text{Br}_2, \text{CCl}_4 \) **c)** Structure: Cyclohexene Reagents: 1) \( \text{BH}_3, \text{THF} \) 2) \( \text{H}_2\text{O}_2, \text{OH}^- \) **d)** Structure: Cyclohexene Reagent: \( \text{NBS} \) Solvent: \( \text{H}_2\text{O, DMSO} \) **e)** Structure: Cyclohexene Reagents: 1) \( \text{Hg(OAc)}_2, \text{H}_2\text{O} \) 2) \( \text{NaBH}_4 \) **f)** Reaction: Cyclohexene + \( \text{CF}_3\text{CO}_3\text{H} \) (Product structure not shown) **g)** Structure: Cyclohexene Reagent: \( \text{H}_2/\text{Pd} \) **h)** Reaction: \[ \begin{array}{l} \ \ \ \ \ \ \ \ \ \text{H} \\ \ \ \ \text{f. } \\ \text{H}_3\text{C} - \text{C} - \text{H} \\ \ \ \ \text{H}_3\text{C} \\ \end{array} \] Reagent: \( \text{KMnO}_4, \text{H}_3\text{O}^+ \) --- This transcription should
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