Starting from the bond-line structure provided, complete the Haworth, Chairs, and Newman structures using the numbering schemes provided. Then, determine which chair conformation is most stable. Briefly explain and illustrate why. Circle each axial substituent in the chair structures. For the Newman projections, the bonds to sight down have been indicated by the numbering scheme provided. For the chairs, you do not need to draw in the hydrogen atoms. For the Newman structures show each substituent clearly and also include the hydrogen atoms only at the carbons indicated with a number. Structures 4 1 2 Haworth Projection Bond-line Structure Chair 1 = Chair 2 = 1C4 Newman - Chair 1 Newman - Chair 1 Most stable chair conformation and explanation:

Starting from the bond-line structure provided, complete the Haworth, Chairs, and Newman structures using the numbering schemes provided. Then, determine which chair conformation is most stable. Briefly explain and illustrate why. Circle each axial substituent in the chair structures. For the Newman projections, the bonds to sight down have been indicated by the numbering scheme provided. For the chairs, you do not need to draw in the hydrogen atoms. For the Newman structures show each substituent clearly and also include the hydrogen atoms only at the carbons indicated with a number. Structures 4 1 2 Haworth Projection Bond-line Structure Chair 1 = Chair 2 = 1C4 Newman - Chair 1 Newman - Chair 1 Most stable chair conformation and explanation:

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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