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An acetone molecule does have a net dipole. The dipole moment of acetone is 2.91 D. This is caused by the difference in electronegativity between methyl groups and a carbonyl group.

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10y ago
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6mo ago

Yes, acetone has a net dipole moment because it is a polar molecule. This is due to the unequal sharing of electrons between the carbon, hydrogen, and oxygen atoms in acetone, resulting in a partial negative charge on the oxygen atom and a partial positive charge on the carbon and hydrogen atoms.

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Q: Does acetone have a net dipole?
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Related questions

What is the inter molecular force in Acetone?

The intermolecular force in acetone (CH3COCH3) is dipole-dipole interaction. This is because acetone contains a carbonyl group that creates a partial negative charge on the oxygen atom and a partial positive charge on the carbon atom, leading to attraction between different acetone molecules.


Is methanol more polar than acetone?

Yes, methanol is more polar than acetone because it has a higher dipole moment and stronger hydrogen bonding capabilities due to its hydroxyl group. Acetone is a less polar solvent compared to methanol.


What type of intermolecular force is acetone?

Acetone exhibits dipole-dipole interactions and London dispersion forces. The oxygen in the carbonyl group of acetone creates a partial negative dipole, while the carbon and hydrogen atoms exhibit London dispersion forces.


What is the intermolecular force of acetone?

Acetone exhibits dipole-dipole interactions as its dominant intermolecular force. This is due to the polar nature of the acetone molecule, which contains a carbonyl group. Additionally, acetone can also experience weak van der Waals forces such as London dispersion forces.


What is net dipole?

The net dipole is the sum of all moment dipoles from a chemical molecule.


An electric dipole is placed in a nonuniform electric filedIs there a net force on the dipole?

Yes, there will be a net force on the electric dipole in a nonuniform electric field. The force will cause a torque on the dipole, leading to its orientation changing in the direction of the field.


Acetone molecules H-bond with other acetones?

Acetone molecules do not typically form hydrogen bonds with other acetone molecules because acetone lacks hydrogen atoms bonded to electronegative atoms like oxygen or nitrogen that are required for hydrogen bonding to occur. Instead, acetone molecules primarily interact through weaker dispersion forces and dipole-dipole interactions.


Does KrBr4 have a net dipole movement?

KrBr4 does not have a net dipole moment because the molecule is symmetrical and the dipole moments of the individual bromine atoms cancel each other out.


Why is actone miscible in water?

Acetone is miscible in water because it can form hydrogen bonds with water molecules through its carbonyl group, making it soluble in water. The polar nature of acetone allows it to interact with the polar water molecules, enabling them to mix easily.


What molecules has no net dipole movement a NH3 b C2H6 c PBr3 d SiO2?

a) NH3: ammonia has a net dipole moment due to the unequal sharing of electrons between nitrogen and hydrogen. b) C2H6: ethane has no net dipole moment because the carbon-carbon and carbon-hydrogen bonds cancel out each other's dipole moments. c) PBr3: phosphorus tribromide has no net dipole moment because the dipole moments of the three P-Br bonds cancel each other out. d) SiO2: silicon dioxide has no net dipole moment due to its symmetrical arrangement of silicon and oxygen atoms.


Does sulfur difluoride have a net dipole moment?

Yes, sulfur difluoride (SF2) does have a net dipole moment because the molecule is angular or bent in shape with uneven distribution of electron density, resulting in an overall dipole moment.


Why perchlorate salt is more soluble in acetone?

Perchlorate salt is more soluble in acetone because acetone is a polar solvent and can effectively interact with the charged ions of the perchlorate salt through dipole-dipole interactions and hydrogen bonding. This interaction helps to stabilize the salt molecules in solution, resulting in higher solubility compared to non-polar solvents.