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The stable form of trans-1, 4 dimethylcy...

The stable form of trans-1, 4 dimethylcyclohexane is represented as:

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To determine the stable form of trans-1,4-dimethylcyclohexane, we will follow these steps: ### Step 1: Understand the Structure Trans-1,4-dimethylcyclohexane has two methyl groups (−CH₃) attached to the cyclohexane ring at the 1 and 4 positions. The "trans" configuration indicates that the two methyl groups are on opposite sides of the ring. ### Step 2: Draw the Cyclohexane Ring Draw a cyclohexane ring. Label the carbon atoms from 1 to 6. ``` C1 / \ C6 C2 | | C5 C3 \ / C4 ``` ### Step 3: Place the Methyl Groups Since we are dealing with trans-1,4-dimethylcyclohexane, we will place one methyl group at carbon 1 and the other at carbon 4. ### Step 4: Determine Axial and Equatorial Positions In a cyclohexane chair conformation, each carbon has one axial and one equatorial position. The axial position is perpendicular to the plane of the ring, while the equatorial position is roughly parallel to the plane. ### Step 5: Identify the Most Stable Configuration To achieve the most stable configuration, bulky groups (like methyl groups) should be placed in the equatorial position to minimize steric hindrance. 1. **Configuration 1**: - Methyl at C1 (equatorial) and methyl at C4 (equatorial) - **Most stable** 2. **Configuration 2**: - Methyl at C1 (axial) and methyl at C4 (equatorial) - Less stable due to steric hindrance. 3. **Configuration 3**: - Methyl at C1 (equatorial) and methyl at C4 (axial) - Less stable due to steric hindrance. 4. **Configuration 4**: - Methyl at C1 (axial) and methyl at C4 (axial) - **Least stable** due to maximum steric hindrance. ### Step 6: Conclusion The most stable form of trans-1,4-dimethylcyclohexane is when both methyl groups are in the equatorial position. Therefore, the correct representation of the stable form is the one where both methyl groups are equatorial. ### Final Answer The stable form of trans-1,4-dimethylcyclohexane is represented as the configuration where both methyl groups are in equatorial positions. ---

To determine the stable form of trans-1,4-dimethylcyclohexane, we will follow these steps: ### Step 1: Understand the Structure Trans-1,4-dimethylcyclohexane has two methyl groups (−CH₃) attached to the cyclohexane ring at the 1 and 4 positions. The "trans" configuration indicates that the two methyl groups are on opposite sides of the ring. ### Step 2: Draw the Cyclohexane Ring Draw a cyclohexane ring. Label the carbon atoms from 1 to 6. ...
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Knowledge Check

  • Which of the following will give a mixture of cis and trans-1,4-dimethyl cyclohexane, when undergo catalytic hydrogenation ?

    A
    B
    C
    D
    Both (a) and (b)
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