Organic Chemistry Maxwell presented by Macmillan Learning Complete the most stable chair conformation of trans-1-tert-butyl-3-methylcyclohexane by filling in the missing atoms. Use the numbering provided on the ring. Answer Bank 6 H. methyl tert-butyl H 14 3 H. H.
Organic Chemistry Maxwell presented by Macmillan Learning Complete the most stable chair conformation of trans-1-tert-butyl-3-methylcyclohexane by filling in the missing atoms. Use the numbering provided on the ring. Answer Bank 6 H. methyl tert-butyl H 14 3 H. H.
Chemistry
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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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Transcribed Image Text:**Organic Chemistry**
Complete the most stable chair conformation of *trans-1-tert-butyl-3-methylcyclohexane* by filling in the missing atoms. Use the numbering provided on the ring.
**Diagram Description:**
The diagram displays a chair conformation of a cyclohexane ring with numbered carbon atoms 1 to 6. The bonds to hydrogen atoms are represented as lines extending from each carbon.
- Carbon 1 has a missing substituent shown by a dashed box.
- Carbon 2 is bonded to a hydrogen atom.
- Carbon 3 is also bonded to a hydrogen atom and has a space for a missing substituent.
- Carbon 4 is shown bonded to a hydrogen atom.
- Carbon 5 is bonded to a hydrogen atom.
- Carbon 6 has a space for a missing substituent.
**Answer Bank:**
- methyl
- tert-butyl
- H
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