Table of Contents
- 1 Which is more acidic p chloro benzoic acid or benzoic acid?
- 2 What is the correct order of acidic strength of benzoic acid O nitrobenzoic acid M nitrobenzoic acid and p-nitrobenzoic acid?
- 3 Which of the following is more acidic in benzoic acid?
- 4 Which of the following is the correct order of acidic strength benzoic acid?
- 5 Which is more acidic para nitro benzoic acid or ortho nitro benzoic acid?
- 6 Which of the following represents the correct order of acidity?
Which is more acidic p chloro benzoic acid or benzoic acid?
Correct explanation: Chlorine has both +R-effect and -I-effect but -I-effect outweighs +R-effect. As a result, p-chlorobenzoic acid is a stronger acid than benzoic acid.
What is the correct order of acidic strength of benzoic acid O nitrobenzoic acid M nitrobenzoic acid and p-nitrobenzoic acid?
The correct order of acid strengths of benzoic acid (X) peroxybenzoic acid (Y) and p-nitrobenzoic acid (Z) is. (c) The acidic strength depends upon the stabilisation the carboxylate ion left after the release of H+ ion by the dispersal of negative charge. Therefore, the correct order is (C).
Which acid is weaker than benzoic acid CLO P methylbenzoic acid p-nitrobenzoic acid O chlorobenzoic acid?
Methyl groups are weak donors and so p-methylbenzoic acid is weaker than benzoic acid. Chlorine is a weak electron donor (by resonance) and hence p-chlorobenzoic acid is slightly stronger than benzoic acid.
Which one is more acidic benzoic acid para nitro benzoic acid para chloro benzoic acid Acetic acid?
p-nitrobenzoic acid is stronger acid than p- chlorobenzoic acid. This is because in p-nitro benzoic acid, nitrogen of nitro group is positively charged and hence electron withdrawing effect of positively charged nitro group is more.
Which of the following is more acidic in benzoic acid?
Benzoic acid is more acidic than acetic acid, formic acid is more acidic than benzoic acid, among monosubstituted benzoic acid derivative, the ortho derivative is more acidic than meta and para substituted acid due to ortho effect. Acidity of an acid can be explained by the stability of conjugated base of acid.
Which of the following is the correct order of acidic strength benzoic acid?
Propanoic acid, chloroethanoic acid, 3-bromo-propanoic acid and trichloroacetic acid.
For which group P is more acidic than benzoic acid?
It is this stabilization provided by the methyl group that makes o-toluic acid a stronger acid (pKa=3.91) than benzoic acid (pKa=4.19).
Which is more acidic benzoic acid or toluic acid?
o-Toluic acid is more acidic than benzoic acid.
Which is more acidic para nitro benzoic acid or ortho nitro benzoic acid?
Hence, nitro group on ortho position has higher inductive effect compared to the nitro group on para position. Therefore, more liberation of H+ is causes the acidity of a compound. Hence, , o-nitrobenzoic acid is more acidic compared to p-nitrobenzoic acid.
Which of the following represents the correct order of acidity?
Thus the acidic strength follows the order: HClO4>HBrO4>HIO4.