neither
CHCl3 is neither an acid nor a base. It is a neutral compound commonly known as chloroform.
Chloroform is not a acid. It is a polar compound.
To extract benzoic acid from chloroform, first dissolve the benzoic acid in water. Then, add chloroform to the mixture and shake well to allow for the benzoic acid to transfer to the chloroform phase. Finally, separate the two phases and evaporate the chloroform to obtain the benzoic acid.
it is soluble in chloroform. Chloroform is nonpolar.
When stearic acid is added to chloroform, it will likely dissolve in the solvent due to its non-polar nature. The stearic acid molecules will form a homogeneous solution with the chloroform molecules, as both are non-polar compounds.
CHCl3 is neither an acid nor a base. It is a neutral compound commonly known as chloroform.
Chloroform is not a acid. It is a polar compound.
To extract benzoic acid from chloroform, first dissolve the benzoic acid in water. Then, add chloroform to the mixture and shake well to allow for the benzoic acid to transfer to the chloroform phase. Finally, separate the two phases and evaporate the chloroform to obtain the benzoic acid.
it is soluble in chloroform. Chloroform is nonpolar.
When stearic acid is added to chloroform, it will likely dissolve in the solvent due to its non-polar nature. The stearic acid molecules will form a homogeneous solution with the chloroform molecules, as both are non-polar compounds.
Yes, acetic acid is soluble in chloroform. Acetic acid is a polar molecule due to its carbonyl group, making it soluble in both polar and nonpolar solvents like chloroform.
Chloroform can be converted into acetone through a series of reactions. Initially, chloroform undergoes oxidative cleavage to form phosgene, which then reacts with water to yield formic acid and hydrochloric acid. Further oxidation of formic acid produces carbon dioxide and water, while hydrochloric acid is neutralized with a base to form water and salt. Finally, the remaining product after this series of reactions is acetone.
Yes, oleic acid is soluble in chloroform due to its non-polar nature. Chloroform is a non-polar solvent, allowing for the dissolution of non-polar compounds like oleic acid.
~13. Evidence: t-butoxide (pKa ~18) can deprotonate it to form dichlorocarbene.
Chloroform reacts with strong acids, such as hydrochloric acid, to form toxic phosgene gas. Phosgene gas is a respiratory irritant and can cause serious health problems if inhaled in high concentrations. Mixing chloroform with an acid should therefore be avoided.
The equation for the reaction of iodine between water and chloroform is: I2 (iodine) + 2CHCl3 (chloroform) ⇌ ICl (iodine monochloride) + 2HCl (hydrochloric acid) + CHCl3 (chloroform).
The reaction of chloroform (CHCl3) and sodium hydroxide (NaOH) results in the formation of sodium trichloromethoxide (NaCCl3) and water (H2O). This reaction is a base-catalyzed halogen exchange reaction, where the chloride ion in chloroform is replaced by the hydroxide ion from sodium hydroxide.