Part 2.2 Having identified the expected products for elimination of cis-1 we can now perform a similar analysis for trans-1. Q8) groups axial or equatorial position clearly shown. Accurately draw the two chair conformations for trans-1 with the alcohol and methyl ОН CH3 trans-1 conformer A conformer B Q9) Which conformer of trans-1 is more stable and why? Q10) appropriate illustration indicate whether the more stable conformer of trans-1 can undergo E2 By considering the stereochemical requirements for E2-elimination, and using an elimination .

Part 2.2 Having identified the expected products for elimination of cis-1 we can now perform a similar analysis for trans-1. Q8) groups axial or equatorial position clearly shown. Accurately draw the two chair conformations for trans-1 with the alcohol and methyl ОН CH3 trans-1 conformer A conformer B Q9) Which conformer of trans-1 is more stable and why? Q10) appropriate illustration indicate whether the more stable conformer of trans-1 can undergo E2 By considering the stereochemical requirements for E2-elimination, and using an elimination .

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter7: Cycloalkanes

Section: Chapter Questions

Problem 17E: Build a model of methylcyclohexane, and use the model to complete the following Newmanprojections of...

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