The structures of two tertiary bicyclic chlorides (compounds 1 and 2) are shown below. Which of the followingstatements is correct?compound 1dcompound 2O a. Compound 1 is more reactive than compound 2 in both substitution and eleiminationO b. Compound 2 is more reactive than compound 1 for both substitution and eleiminationO c. On treatment with KOH in ethanol, compound 1 undergoes substitution and compound 2 undergoeseliminationO d. On treatment with KOH in ethanol, both compounds undergo E2 elimination

Bredt's rule states that a carbon cannot be sp2 hybridized at the bridge head position which means…

Answered: The structures of two tertiary bicyclic…

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The structures of two tertiary bicyclic chlorides (compoun statements is correct? CI

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter9: Nucleophilic Substitution And Β-elimination

Section: Chapter Questions

Problem 9.48P: The Williamson ether synthesis involves treatment of a haloalkane with a metal alkoxide. Following...

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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

The structures of two tertiary bicyclic chlorides (compounds 1 and 2) are shown below. Which of the following
statements is correct?
compound 1
d
compound 2
O a. Compound 1 is more reactive than compound 2 in both substitution and eleimination
O b. Compound 2 is more reactive than compound 1 for both substitution and eleimination
O c. On treatment with KOH in ethanol, compound 1 undergoes substitution and compound 2 undergoes
elimination
O d. On treatment with KOH in ethanol, both compounds undergo E2 elimination

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