You might be referring to the Fischer-Speier reaction for producing ethyl ethanoate from the other two substances. The other product is water. By contriving to eliminate the water it is possible to favour the equilibrium of this reaction toward more of the desired substance. Please see the link for methods.
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).
Yes, it is because it has carbon in it. That is the basic element found in all organic compounds. There classes in college called Organic Chemistry which deal with these compounds.
Yes, it is because it has carbon in it. That is the basic element found in all organic compounds. There classes in college called Organic Chemistry which deal with these compounds.
Organic chemistry is the chemistry of compounds of Carbon. Carbon is [almost] unique in its ability to form -C-C-C-C-C- etc. chains. Attach Hydrogens, and the basic structural bio-unit is -CH2- .
These organic substances are called amines.
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).
weak acid.
When ethanol and benzoic acid combine, the products depend on the reaction conditions. Under acidic conditions, esterification can occur producing ethyl benzoate and water. Under basic conditions, the sodium salt of benzoic acid may form.
The reaction between benzoic acid and zinc oxide does not lead to a simple single equation because benzoic acid is a weak acid that does not readily form salts with metals like zinc. However, if the reaction were to occur, it might involve the displacement of hydrogen from benzoic acid by zinc to form zinc benzoate and hydrogen gas.
Carbon is the basic constituent of all organic matter. Organic compounds are made up of carbon in combination with hydrogen, oxygen, nitrogen, and other elements.
salt.
Carbon.
Carbon is the basic element.It should be in compound to be organic
Carbon
Sodium benzoate (NaC6H5CO2) is the salt of benzoic acid, which is a weak acid. Therefore, when dissolved in water, it will be slightly basic due to the formation of hydroxide ions from the reaction between the sodium ions and water.
They are nonreactive towards each other in aqueous solutions but separately in acidic medium sodium benzoate forms the benzoic acid and ammonium chloride forms ammonia in basic medium.
D.J Abbott has written: 'Organic chemistry; the basic reactions' -- subject(s): Chemistry, Organic, Organic Chemistry