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.

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**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
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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