10. Predict the product(s) of the following reaction, indicating stereochemistry where necessary: 1-chloro-1,4-diethylcyclohexane (the cthyl groups are trans to each other) reacting with WATER in methanol (solvent).

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**Educational Content: Organic Chemistry Reactions**

**10. Reaction Prediction**
- Predict the product(s) of the following reaction, indicating stereochemistry where necessary:
  - **Reactant**: 1-chloro-1,4-diethylcyclohexane (the ethyl groups are trans to each other).
  - **Reactants/Conditions**: Water in methanol (solvent).

**11. Major Product Prediction**
- Predict the major products of each reaction. Identify the chiral products, if any.

  a. **cis-4-ethylcyclohexanol** (as tosylate for ease of leaving) reacting with \(-CN\).
  
  b. \((R)\) **2-chloro-2,3-dimethylhexane** with ethoxide anion in ethanol.
  
  c. **1-bromo-2,3-dimethylcyclohexane** (methyl groups cis to each other, dash/dash) in ethanol (solvent).

**12. Synthesis Using Substitution**
- Synthesize the following using appropriate (\(S_N1\) or \(S_N2\)) substitution at some point in the synthetic route:

  a. **1-aminobutane**

  b. **t-butyl methyl ether** (a very dangerous compound)

  c. **(CH₃)₂CCHCN**
Transcribed Image Text:**Educational Content: Organic Chemistry Reactions** **10. Reaction Prediction** - Predict the product(s) of the following reaction, indicating stereochemistry where necessary: - **Reactant**: 1-chloro-1,4-diethylcyclohexane (the ethyl groups are trans to each other). - **Reactants/Conditions**: Water in methanol (solvent). **11. Major Product Prediction** - Predict the major products of each reaction. Identify the chiral products, if any. a. **cis-4-ethylcyclohexanol** (as tosylate for ease of leaving) reacting with \(-CN\). b. \((R)\) **2-chloro-2,3-dimethylhexane** with ethoxide anion in ethanol. c. **1-bromo-2,3-dimethylcyclohexane** (methyl groups cis to each other, dash/dash) in ethanol (solvent). **12. Synthesis Using Substitution** - Synthesize the following using appropriate (\(S_N1\) or \(S_N2\)) substitution at some point in the synthetic route: a. **1-aminobutane** b. **t-butyl methyl ether** (a very dangerous compound) c. **(CH₃)₂CCHCN**
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