Textbook Question
Which has
h. the higher boiling point: diethyl ether or butyl alcohol?
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2. Molecular Representations
Intermolecular Forces
5:32 minutesProblem 5c,d
Textbook Question
For each pair of compounds, predict which one has the higher molecular dipole moment, and explain your reasoning.
c. cis-2,3-dibromobut-2-ene or trans-2,3-dibromobut-2-ene
d. cis-1,2-dichlorocyclobutane or trans-1,3-dichlorocyclobutane
Verified step by step guidance1
Step 1: Understand the concept of molecular dipole moment. The dipole moment is a measure of the separation of positive and negative charges in a molecule. It depends on both the magnitude of the individual bond dipoles and their spatial arrangement.
Step 2: Analyze the structure of cis-2,3-dibromobut-2-ene. In the cis isomer, the bromine atoms are on the same side of the double bond, which can lead to a net dipole moment as the bond dipoles do not cancel out completely.
Step 3: Analyze the structure of trans-2,3-dibromobut-2-ene. In the trans isomer, the bromine atoms are on opposite sides of the double bond, which often results in the bond dipoles canceling each other out, leading to a lower or zero net dipole moment.
Step 4: Compare the dipole moments of cis-1,2-dichlorocyclobutane and trans-1,3-dichlorocyclobutane. In the cis isomer, the chlorine atoms are on the same side of the cyclobutane ring, which can result in a net dipole moment. In the trans isomer, the chlorine atoms are on opposite sides, which may lead to cancellation of dipole moments.
Step 5: Conclude that the molecular geometry and the relative positions of the substituents (cis vs. trans) significantly affect the net dipole moment. Generally, cis isomers tend to have higher dipole moments than their trans counterparts due to less cancellation of bond dipoles.
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Video duration:
5mKey Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Molecular Dipole Moment
The molecular dipole moment is a measure of the overall polarity of a molecule, determined by the vector sum of all individual bond dipoles. It depends on both the magnitude of the bond dipoles and their spatial arrangement. Molecules with symmetrical arrangements of polar bonds may have a net dipole moment of zero, while asymmetrical arrangements can result in a higher dipole moment.
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Cis-Trans Isomerism
Cis-trans isomerism, a type of stereoisomerism, occurs in compounds with restricted rotation around a bond, such as double bonds or in cyclic structures. In cis isomers, similar or identical groups are on the same side, leading to potential dipole moments due to asymmetry. In trans isomers, these groups are on opposite sides, often resulting in cancellation of dipole moments due to symmetry.
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Effect of Substituents on Cycloalkanes
In cycloalkanes, the spatial arrangement of substituents significantly affects the molecule's dipole moment. Substituents in a cis configuration can create a net dipole moment due to their additive effect, while in a trans configuration, the dipoles may cancel out. The position and type of substituents, along with the ring strain, influence the overall molecular polarity.
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