#11 **Educational Website Content:****Chemistry Reaction Problems and Synthesis Tasks****10. Reaction Prediction:**Predict the product(s) of the following reaction, indicating stereochemistry where necessary:- **Reactants:** 1-chloro-1,4-diethylcyclohexane (the ethyl groups are trans to each other) - **Reagents/Solvent:** Reacting with WATER in methanol (solvent).**11. Major Products Prediction:**Predict the major products of each reaction. Identify the chiral products, if any.a. **cis-4-ethylcyclohexanol** (as tosylate for ease of leaving) + CN⁻ b. **(R) 2-chloro-2,3-dimethylhexane** + ethoxide anion in ethanol c. **1-bromo-2,3-dimethylcyclohexane** (methyl groups cis to each other, dash/dash) in ethanol (solvent)**12. Synthesis Tasks:**Synthesize using appropriate (SN1 or SN2) substitution at some point in the synthetic route.a. **1-aminobutane** b. **(Very dangerous compound) t-butyl methyl ether** c. **(CH₃)₂CCHCN** **Note:** There are no graphs or diagrams included in the provided text.

As per the rules only first question can be answered.

11. Predict the major products of each reaction. Identify the chiral products, if any. a. cis-4-ethyleyclohexanol (as tosylate for ease of leaving) +-CN> b. (R) 2-chloro-2,3-dimethylhexane + ethoxide anion in ethanol → c. 1-bromo-2,3-dimethyleyclohexane (methyl groups cis to each other, dash/dash) > in ethanol (solvent)

11. Predict the major products of each reaction. Identify the chiral products, if any. a. cis-4-ethyleyclohexanol (as tosylate for ease of leaving) +-CN> b. (R) 2-chloro-2,3-dimethylhexane + ethoxide anion in ethanol → c. 1-bromo-2,3-dimethyleyclohexane (methyl groups cis to each other, dash/dash) > in ethanol (solvent)

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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