CuSO4 is ionic and water is polar. The types of bonding allow water to dissolve the salt much more easily than an organic solvent (e.g. alcohol, hexane) could.
Water and copper sulfate are both polar compound; polar compounds are dissolved better in polar solvents. Salycilic acid is also polar but the solubility is lower because the benzene ring has a negative effect.
No. Kerosene is an organic compound. and water is a non-organic compound. (kerosene : non-polar Water : polar). As water is a polar solvent kerosene is not soluble in it. but kerosene is soluble in ethyl alcohol which is a non-polar solvent.
The chemical structure of phenobarbital is:The aromatic ring and methyl group will be more favorable for organic solvent, while the NH in the ring and O attachments favor aqueous solvents.One gram is soluble in approximately 1000 ml of water, and 10 ml of alcohol. Compared to other barbiturates it has a lowlipid solubility. It is very soluble in water, soluble in alcohol, and freely solu­ble in propylene glycol. In other words, the question makes an incorrect assumption - phenobarbital is MORE soluble in aqueous solvents than in organic solvents.
Diphenylamine is only slightly soluble in water, but more soluble in polar organic solvents.
No, it won't. Organic fat is made up of lipids that are not water soluble and so can't dissolve in water.
hydrocarbons are not soluble in a polar solvent but are soluble in a non-polar solvent.
CuSO4 is water soluble. CaCO3 is not.
No. Kerosene is an organic compound. and water is a non-organic compound. (kerosene : non-polar Water : polar). As water is a polar solvent kerosene is not soluble in it. but kerosene is soluble in ethyl alcohol which is a non-polar solvent.
Iron oxide is only soluble when placed in concentrated mineral acids. It is insoluble in organic and water based solvents.
Lipids are soluble in nonpolar or organic solvents.
No water soluble pepper is already organic.
water because quinidine is water soluble, being an organic substance used in the body and dissolved by a glass of water taken with the medication, whereas BaSO4 is not water soluble at all
The chemical structure of phenobarbital is:The aromatic ring and methyl group will be more favorable for organic solvent, while the NH in the ring and O attachments favor aqueous solvents.One gram is soluble in approximately 1000 ml of water, and 10 ml of alcohol. Compared to other barbiturates it has a lowlipid solubility. It is very soluble in water, soluble in alcohol, and freely solu­ble in propylene glycol. In other words, the question makes an incorrect assumption - phenobarbital is MORE soluble in aqueous solvents than in organic solvents.
chlorophyll is more soluble than xanthophyll
Diphenylamine is only slightly soluble in water, but more soluble in polar organic solvents.
Well, usually when you ask that question, you specify what solvent to which you are referring. e.g. "Is pyrite soluble in toluene?" I will assume what you mean is "Is pyrite soluble in water?" as water is the universal solvent. And the answer is no
No, it won't. Organic fat is made up of lipids that are not water soluble and so can't dissolve in water.
hydrocarbons are not soluble in a polar solvent but are soluble in a non-polar solvent.