Barbituric acid looks like its very polar... it should be soluble in water and acetone, at least.
Visualizing it on a TLC plate is problematic because the compound is not aromatic and thus does not absorb UV. The easiest way to visualize non-UV absorbing compounds on a TLC plate is using an iodine development chamber. In a jar, mix some powdered iodine (I2) crystals* and dry silica gel. Throw in the TLC plate (after running in the appropriate solvent system), shake it a bit, and use forceps to fish it out. The iodine should oxidize the compound on the plate and it should appear as a brown dot. The iodine development chamber can be used pretty much indefinitely. Hope this helps!
It depends upon solvent with respect to water, alkenes are not soluble. Carboxylic Acid are soluble but they become less soluble as the chain length increases due to the longer non-polar hydrocarbon chain which can't form hydrogen bonds with water.
Formic acid is partially soluble in water
because it is derived from barbituric acid which is known of it's acidity by losing the [H] on the Beta carbon striking down the PH to around 5
not soluble but can be converted into an acid soluble salt
solvent acid solut frog
Generally, it is soluble in HF, hydrofluoric acid.
The conjugate acid is a salt. The ionic character of the salt makes it soluble in water, a polar solvent.
Succinic acid may be slightly soluble in hexane, but not to a useful extent. Succinic acid would be better suited for a solvent that it can hydrogen bond with due to its hydroxyl groups.
Silver is soluble in Nitric Acid producing silver nitrate.
Barbituric acid is the common chemical component of barbiturates.
Don't know :z hurry up and answer so i can finish my homework? Don't know :z hurry up and answer so i can finish my homework?
there are number of inorganic solvents, such sulphuric acid, that will act as a solvent that will dissolve tin
It depends upon solvent with respect to water, alkenes are not soluble. Carboxylic Acid are soluble but they become less soluble as the chain length increases due to the longer non-polar hydrocarbon chain which can't form hydrogen bonds with water.
water b/c it is insoluble in water. it is soluble in cyclohexane and sparingly soluble in ethyl alcohol.
barbituric acid, luminal, equinil, vernola etc are examples for tranquilizers
I can't find a number, but I found this: Benzoic acid is slightly soluble in water, soluble in ethanol, very slightly soluble in benzene and acetone. (see link on the left under Web Links) This implies not very much benzoic acid will dissolve in benzene. This other site (the MSDS for benzoic acid) says this: SOLVENT SOLUBILITY: Soluble in alcohol, ether, benzene, chloroform, acetone, carbon disulfide, oil of turpentine, carbon tetrachloride, fixed and volatile oils; slightly soluble in petroleum ether, hexane. This does make it sound fairly soluble! Hard to say which is right. This can easily be determined by experiment however!
Absolutely not! Using gasoline as a solvent, wax dissolves in it but glass will not dissolve at all. Using water as a solvent, salt dissolves in it but pepper will not dissolve at all. Using hydrofluoric acid as a solvent, glass dissolves in it but wax will not dissolve at all.