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The molecules having dipole moment are :...

The molecules having dipole moment are :

A

2,2-Dimethylpropane

B

trans-Pent-2-ene

C

cis-Hex-3-ene

D

2,2,3,3-Tetramethylbutane

Text Solution

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The correct Answer is:
To determine which molecules have dipole moments, we need to analyze the molecular structures and the arrangement of their bonds. A dipole moment arises in a molecule when there is an uneven distribution of electron density, typically due to differences in electronegativity between atoms. Here’s a step-by-step breakdown of the given question: ### Step 1: Analyze 2,2-Dimethylpropane 1. **Structure Drawing**: 2,2-Dimethylpropane has a three-carbon chain (propane) with two methyl groups attached to the second carbon. - Structure: ``` CH3 | CH3 - C - CH3 | CH3 ``` 2. **Dipole Moment Analysis**: The dipole moments from the methyl groups will cancel each other out because they are symmetrically placed around the central carbon atom. 3. **Conclusion**: The dipole moment for 2,2-dimethylpropane is zero. ### Step 2: Analyze Trans-Pent-2-ene 1. **Structure Drawing**: Trans-pent-2-ene has a double bond between the second and third carbon atoms, with a methyl group on one side and an ethyl group on the other. - Structure: ``` CH3 - C = C - CH2 - CH3 ``` 2. **Dipole Moment Analysis**: The methyl and ethyl groups create a dipole moment that does not cancel out because they have different electronegativities. 3. **Conclusion**: Trans-pent-2-ene has a net dipole moment. ### Step 3: Analyze Cis-Hex-3-ene 1. **Structure Drawing**: Cis-hex-3-ene has a double bond between the third and fourth carbon atoms, with both methyl and ethyl groups on the same side of the double bond. - Structure: ``` CH3 - CH = CH - CH2 - CH3 ``` 2. **Dipole Moment Analysis**: The dipole moments from the methyl and ethyl groups do not cancel out due to their different sizes and electronegativities. 3. **Conclusion**: Cis-hex-3-ene has a net dipole moment. ### Step 4: Analyze 2,2,3,3-Tetramethylbutane 1. **Structure Drawing**: 2,2,3,3-Tetramethylbutane has a four-carbon chain with two methyl groups on the second carbon and two on the third. - Structure: ``` CH3 | CH3 - C - C - CH3 | | CH3 CH3 ``` 2. **Dipole Moment Analysis**: The symmetrical arrangement of the methyl groups means that all dipole moments will cancel out. 3. **Conclusion**: The dipole moment for 2,2,3,3-tetramethylbutane is zero. ### Final Conclusion From the analysis: - **Molecules with dipole moments**: Trans-pent-2-ene and Cis-hex-3-ene. - **Molecules without dipole moments**: 2,2-dimethylpropane and 2,2,3,3-tetramethylbutane. ### Answer: The molecules having dipole moments are **Trans-pent-2-ene and Cis-hex-3-ene**. ---

To determine which molecules have dipole moments, we need to analyze the molecular structures and the arrangement of their bonds. A dipole moment arises in a molecule when there is an uneven distribution of electron density, typically due to differences in electronegativity between atoms. Here’s a step-by-step breakdown of the given question: ### Step 1: Analyze 2,2-Dimethylpropane 1. **Structure Drawing**: 2,2-Dimethylpropane has a three-carbon chain (propane) with two methyl groups attached to the second carbon. - Structure: ``` CH3 | ...
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