#12 10. Prediet the product(s) of the following reaction, indicating stereochemistry wherenecessary:1-chloro-1,4-diethylcyclohexane (the ethyl groups are trans to each other) reacting withWATER in methanol (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)12. Synthesize using appropriate (SN1 or SN2) substitution at some point in synthetic route.a. 1-aminobutaneb. (very dangerous compound) -buty! methyl etherc. (CH3)CHCN

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Answered: 12. Synthesize using appropriate (SNl…

12. Synthesize using appropriate (SNl or SN2) substitution at some point in synthetic route. a. 1-aminobutane b. (very dangerous compound) -butyl methyl ether c. (CH;)CHCN

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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Question

#12

10. Prediet the product(s) of the following reaction, indicating stereochemistry where
necessary:
1-chloro-1,4-diethylcyclohexane (the ethyl groups are trans to each other) reacting with
WATER in methanol (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)
12. Synthesize using appropriate (SN1 or SN2) substitution at some point in synthetic route.
a. 1-aminobutane
b. (very dangerous compound) -buty! methyl ether
c. (CH3)CHCN

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