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How does orthoboric acid react with ethyl alcohol?
The chemical equation is:H3BO3 + 3 C2H5OH = (C2H5O)3 + 3 H2O
What acid is in borax?
Borax contains the weakly acidic boric acid, also known as orthoboric acid.
What is the difference between ortho-phosphoric acid and phosphoric acid?
Ortho-phosphoric acid is a specific form of phosphoric acid, where the phosphorus atom is bonded to three hydroxyl groups. Phosphoric acid, on the other hand, is a more general term that can refer to any acid containing phosphorus, including ortho-phosphoric acid, as well as pyrophosphoric acid and metaphosphoric acid.
Is Ortho-nitrobenzoic acid more acidic than meta-nitrobenzoic acid?
Yes, ortho-nitrobenzoic acid is more acidic than meta-nitrobenzoic acid due to the presence of the nitro group at the ortho position, which stabilizes the conjugate base through resonance, making it easier to donate a proton.
Why ortho chlorobenzoic acid is stronger than benzoic acid?
Ortho chlorobenzoic acid is stronger than benzoic acid due to the electron-withdrawing effect of the chlorine atom. This increases the acidity of ortho chlorobenzoic acid by stabilizing the conjugate base through delocalization of the negative charge. In contrast, benzoic acid has no such electron-withdrawing substituent.
Can orthoboric acid kill bed bugs?
no,but it can harm humans
How does orthoboric acid react with ethyl alcohol?
The chemical equation is:H3BO3 + 3 C2H5OH = (C2H5O)3 + 3 H2O
What acid is in borax?
Borax contains the weakly acidic boric acid, also known as orthoboric acid.
Does boric acid contain starch?
The simple answer is No. Boric acid is also called hydrogen borate, boracic acid or orthoboric acid. It is an inorganic compound and has the chemical formula H3BO3. There is no starch (an organic ommpound) in boric acid.
What is the difference between ortho-phosphoric acid and phosphoric acid?
Ortho-phosphoric acid is a specific form of phosphoric acid, where the phosphorus atom is bonded to three hydroxyl groups. Phosphoric acid, on the other hand, is a more general term that can refer to any acid containing phosphorus, including ortho-phosphoric acid, as well as pyrophosphoric acid and metaphosphoric acid.
Is Ortho-nitrobenzoic acid more acidic than meta-nitrobenzoic acid?
Yes, ortho-nitrobenzoic acid is more acidic than meta-nitrobenzoic acid due to the presence of the nitro group at the ortho position, which stabilizes the conjugate base through resonance, making it easier to donate a proton.
Ortho effect on acidity of carboxylic acid?
The ortho effect refers to the decrease in acidity of a carboxylic acid when bulky substituents are present at the ortho positions of the phenyl ring. This is due to the steric hindrance caused by the bulky groups, which makes it more difficult for the carboxylate anion to be stabilized, resulting in lower acidity.
Why ortho chlorobenzoic acid is stronger than benzoic acid?
Ortho chlorobenzoic acid is stronger than benzoic acid due to the electron-withdrawing effect of the chlorine atom. This increases the acidity of ortho chlorobenzoic acid by stabilizing the conjugate base through delocalization of the negative charge. In contrast, benzoic acid has no such electron-withdrawing substituent.
Salicylic acid is ortho para directing group or meta directing group?
salicytic acid is a ortho para directing group ....however check up on that ...i am not completely certain .. Actually, it is a meta-directing group, because of the carboxylic acid functional that the salicylic acid contains. Hope that was helpful.
What has the author Marion Byrd Hopkins written?
Marion Byrd Hopkins has written: 'The chlorides of ortho-sulpho-benzoic acid ..' -- subject(s): Chlorides, Sulphobenzoic acid, Ortho-
How does ortho boric acid reacts with ethanol?
When ortho boric acid reacts with ethanol, it forms boric acid esters (borate esters) and water. The reaction involves the alcohol group of ethanol replacing one of the hydroxyl groups in ortho boric acid, resulting in the formation of ester linkages. Boric acid esters are commonly used as catalysts in organic synthesis reactions.
Which is more acidic ortho-nitro benzoic acid or ortho-methoxy benzoic acid?
Ortho-nitrobenzoic acid is more acidic than ortho-methoxybenzoic acid because the nitro group is an electron-withdrawing group that stabilizes the negative charge on the conjugate base through resonance, making it easier to lose a proton. The methoxy group, on the other hand, is an electron-donating group that destabilizes the conjugate base, making it less acidic.
