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Draw the cis and trans structures of hex...

Draw the cis and trans structures of hex-2-ene. Which isomer will have higher b.p. and why?

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To solve the problem of drawing the cis and trans structures of hex-2-ene and determining which isomer has a higher boiling point, we can follow these steps: ### Step 1: Understand the structure of hex-2-ene Hex-2-ene is an alkene with six carbon atoms and a double bond between the second and third carbon atoms. The general formula for alkenes is CnH2n, so for hex-2-ene (C6H12), we can visualize the structure. ### Step 2: Draw the carbon skeleton 1. Start with a straight chain of six carbon atoms: ``` C1 - C2 - C3 - C4 - C5 - C6 ``` ### Step 3: Add the double bond 2. Place a double bond between the second and third carbon atoms: ``` C1 - C2 = C3 - C4 - C5 - C6 ``` ### Step 4: Add hydrogen atoms 3. Add hydrogen atoms to satisfy the tetravalency of carbon. The structure will look like this: - C1: CH3 - C2: CH (with one hydrogen and one alkyl group) - C3: CH (with one hydrogen and one alkyl group) - C4: CH2 - C5: CH2 - C6: CH3 So the complete structure is: ``` CH3 - CH = CH - CH2 - CH2 - CH3 ``` ### Step 5: Draw the cis isomer 4. For the cis isomer, the two substituents (hydrogens) on the double bond will be on the same side: ``` H H \ / C = C / \ CH3 CH2-CH2-CH3 ``` ### Step 6: Draw the trans isomer 5. For the trans isomer, the two substituents (hydrogens) on the double bond will be on opposite sides: ``` H CH3 \ / C = C / \ CH3 H ``` ### Step 7: Compare boiling points 6. To determine which isomer has a higher boiling point, we need to consider the polarity of the molecules: - The cis isomer has a higher dipole moment due to the arrangement of the substituents, leading to stronger intermolecular dipole-dipole interactions. - The trans isomer has a lower dipole moment because the dipoles cancel each other out. ### Conclusion 7. Therefore, the cis isomer of hex-2-ene will have a higher boiling point than the trans isomer due to its greater polarity and stronger intermolecular forces. ### Summary of the Solution: - The cis structure has both hydrogen atoms on the same side of the double bond, while the trans structure has them on opposite sides. - The cis isomer has a higher boiling point due to stronger dipole-dipole interactions resulting from its polar nature.

To solve the problem of drawing the cis and trans structures of hex-2-ene and determining which isomer has a higher boiling point, we can follow these steps: ### Step 1: Understand the structure of hex-2-ene Hex-2-ene is an alkene with six carbon atoms and a double bond between the second and third carbon atoms. The general formula for alkenes is CnH2n, so for hex-2-ene (C6H12), we can visualize the structure. ### Step 2: Draw the carbon skeleton 1. Start with a straight chain of six carbon atoms: ``` ...
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