It depends on the overall reaction. If the carboxylic acid is an impurity in the reaction (undesired), then washing with sodium hydroxide will extract the carboxylic into the aqueous layer, and it can then be disposed. The reaction for this looks as follows:
(ring)-COOH + NaOH -> (ring)-COO-Na+ + H20
Where the ring loses a proton to the hydroxide ion and becomes water soluble.
In this step of the experiment you are trying to separate benzoic acid from biphenyl an impurity. Sodium hydroxide reacts with benzoic acid to form (ar-O-O(-)na(+)) and (H2O), this allows for the ether layer containing biphenyl to separate as the precipitant, which we can now extract and discard.
Sodium hydroxide, commonly used in sodium extraction processes, is a strong base that contributes to the alkaline nature of the extract. When sodium hydroxide dissociates in water, it releases hydroxide ions which increase the pH of the solution, making it alkaline.
Ammonium hydroxide can be used to capture CO2 through a process known as carbon capture and storage (CCS). In this process, the CO2 is absorbed by the ammonium hydroxide solution, forming ammonium carbonate. The ammonium carbonate can then be further processed to extract the CO2 for storage or utilization.
We need to prepare sodium extract for the detection of foreign elements because foreign elements are found in organic compound bonded covalently. As a result they cannot be detected through organic compound directly. Hence they are first converted into ionic compound with the help of sodium extract
Washing monomer methyl methacrylate with sodium hydroxide helps to remove any acidic impurities present. Following this with sodium chloride helps to extract any remaining impurities and water from the product. This process helps to purify the monomer for further use in polymerization reactions.
In this step of the experiment you are trying to separate benzoic acid from biphenyl an impurity. Sodium hydroxide reacts with benzoic acid to form (ar-O-O(-)na(+)) and (H2O), this allows for the ether layer containing biphenyl to separate as the precipitant, which we can now extract and discard.
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.
Make a solution of Sodium Hydroxide or Sodium Carbonate and do three to four solvent solvent extractions using the aqueous base and the mixture o benzoic acid and toluene. Because benzoic acid reacts with base to form the water soluble carboxylate ion, it will react and the dissolve in the aqueous solution. Upon separation of the two phases acidify the aqueous extract with dilute HCl, a white needle-like precipitate of benzoic acid will form when the solution becomes acidic. Simply filter the crystals, wash with cold water, and then recrystallize using a mixture of 50/50 water and methanol or some other suitable solvent.
Yes, benzoic acid will react with sodium bicarbonate to produce sodium benzoate, carbon dioxide, and water. This reaction can be used to extract benzoic acid from a mixture as it is relatively insoluble in water but soluble in sodium bicarbonate solution.
When you're attempting to extract benzoic acid from other organic compounds, it is necessary to change its pH by adding a layer of an basic compound such as 1M NaOH so that the benzoic acid then can be separated from the organic layer within a separatory funnel. When in NaOH, the benzoic acid loses a proton and thus becomes its conjugate base (the benzoate ion). The benzoate ion is charged and thus become miscible in the aqueous layer. To extract benzoic acid (ie get it to precipitate out of solution), a strong acid such as HCl must be added to solution. After the extraction, lower the pH of the solution, and recrystalize (use ice after the recrystalization to get benzoic acid crystals to crash out).
Violet
Because this solution contain sodium hydroxide.
Sodium hydroxide, commonly used in sodium extraction processes, is a strong base that contributes to the alkaline nature of the extract. When sodium hydroxide dissociates in water, it releases hydroxide ions which increase the pH of the solution, making it alkaline.
The ingredients in Proactiv toner are Aloe Vera, Chamomile Extract, Panthenol, Allantoin, and Witch Hazel Extract. The toner also contains propylparaben, sodium hydroxide,glycerin, glycolic acid, and anthemis nobilis flower extract.
The necessary technological conditions did not exist.
Dissolve the mixture in an apolar organic solvent, such as diethyl ether, and extract the acid with the addition of NaOH. The bezoic acid with ionize and go into the aqueous solution. Separate the two layers and add HCl to the aqueous layer to precipitate the benzoic acid. Wash the remaing ether solution with water and dry it with an anhydrous salt. Filter the ether solution and then remove the ether, the solvent, in order to obtain the pure benzoin.
It is because sodium reacts with water (present in test tube or porcelain basin) to give a alkaline solution of NaOH.