chloroform is more polar than hexane. Based from the solvent polarity chart, alkyl halides (such as CHCl3) are relatively more polar than alkanes (such as hexane). Moreso, alkanes tend to be the least polar among the organic and inorganic compounds due to their hydrocarbon structure.
Chloroform is stronger in dissolving lipids compared to hexane because chloroform has a higher polarity due to the presence of electronegative chlorine atoms. This polarity allows chloroform to interact more effectively with lipid molecules, which generally have polar and nonpolar regions, making them more soluble in chloroform than in hexane.
yes toluence is more polar than chloroform
10g of chloroform has a greater volume than 10g of hexane because chloroform has a higher density than hexane. Density is a measure of mass per unit volume, so for the same mass, the substance with the higher density will occupy less volume.
Chloroform is more polar than dichloromethane (DCM) due to the presence of a stronger dipole moment caused by its more electronegative chlorine atoms. This makes chloroform more soluble in polar solvents compared to DCM.
Yes, chloroform is more polar than ethyl acetate. Chloroform has a higher dipole moment due to the greater difference in electronegativity between the carbon and chlorine atoms, making it more polar than ethyl acetate.
Chloroform is stronger in dissolving lipids compared to hexane because chloroform has a higher polarity due to the presence of electronegative chlorine atoms. This polarity allows chloroform to interact more effectively with lipid molecules, which generally have polar and nonpolar regions, making them more soluble in chloroform than in hexane.
yes toluence is more polar than chloroform
10g of chloroform has a greater volume than 10g of hexane because chloroform has a higher density than hexane. Density is a measure of mass per unit volume, so for the same mass, the substance with the higher density will occupy less volume.
No, hexane molecules are non-polar.
Chloroform is more polar than dichloromethane (DCM) due to the presence of a stronger dipole moment caused by its more electronegative chlorine atoms. This makes chloroform more soluble in polar solvents compared to DCM.
No, hexane is less polar than dichloromethane. Hexane is a nonpolar solvent because it contains only carbon and hydrogen atoms, while dichloromethane has polar covalent bonds due to the presence of chlorine atoms.
Yes, chloroform is more polar than ethyl acetate. Chloroform has a higher dipole moment due to the greater difference in electronegativity between the carbon and chlorine atoms, making it more polar than ethyl acetate.
Ethanol is polar, as the non-polar OH group still exerts enough force over the rest of the chain to make the entire hydrocarbon dissolve. This trend continues with alcohols with one carbon (methanol) two carbons (ethanol) three carbons (propanol) and four carbons (butanol). However, butanol is only polar when the OH functional group is attached to a secondary carbon (i.e. butan-2-ol) Hexane is always non-polar, as it is a symmetrical hydrocarbon (like most of them) which means that all forces cancel each other out. So ethanol is more polar than hexane.
Hexane is a non-polar solvent, so it will not dissolve in water. Kerosene is non-polar so it will dissolve in Hexane.
Potassium manganate 7 is more soluble in hexane than in water because it is a nonpolar solvent like hexane. Nonpolar solutes tend to dissolve better in nonpolar solvents, while water is a polar solvent. Therefore, the solubility of potassium manganate 7 is higher in hexane than in water.
Chloroform is more polar than carbon tetrachloride. This is because chloroform has a dipole moment due to the electronegativity difference between carbon and chlorine atoms, while carbon tetrachloride is nonpolar as the four chlorine atoms cancel out any dipole moments.
Yes, chloroform is soluble in ethanol. Chloroform is a non-polar solvent, while ethanol is a polar solvent. When mixed together, the non-polar chloroform will dissolve in the polar ethanol due to their differing solubility properties.