C ) Using chair conformational structure, show the nucleophilic substitutionreaction that would take place when trans-1-bromo-4-tert-butylcyclohexane react with iodideion. (Show the most stable conformation of the reactant and product)

Trans-1-bromo-4-tert-butyl cyclohexane on reaction with iodide ions(I -) follows SN2 mechanism and…

Answered: ) Using chair conformation action that…

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) Using chair conformation action that would take place when trans- n. (Show the most stable conformation o

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 40CTQ

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Concept explainers

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.

Question

C ) Using chair conformational structure, show the nucleophilic substitution
reaction that would take place when trans-1-bromo-4-tert-butylcyclohexane react with iodide
ion. (Show the most stable conformation of the reactant and product)

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