Advertisements
Advertisements
प्रश्न
Which one of the following has the lowest pKa value?
विकल्प
CH3 – COOH
O2N–CH2–COOH
Cl–CH2–COOH
HCOOH
Advertisements
उत्तर
O2N–CH2–COOH
Explanation:
It is simpler to remove an electron since the –NO2 group is an electron-withdrawing group. As a result, the acidity is stronger, and the pKa value is lower.
APPEARS IN
संबंधित प्रश्न
Write the equation involved in the acetylation of Salicylic acid.
Explain how does the −OH group attached to a carbon of benzene ring activate it towards electrophilic substitution?
Intermolecular hydrogen bonding is strongest in ______.
Acidity of phenol is due to ____________.
Mark the correct order of decreasing acid strength of the following compounds.
| (a) | ![]() |
| (b) | ![]() |
| (c) | ![]() |
| (d) | ![]() |
| (e) | ![]() |
Out of o-nitrophenol and o-cresol which is more acidic?
Arrange the following in the increasing order of their property indicated:
4-Nitrobenzoic acid, benzoic acid, 3,4-Dinitrobenzoic acid, 4-Methoxy benzoic acid (Acid strength)
In the following compounds:
![]() |
![]() |
![]() |
![]() |
| (I) | (II) | (III) | (IV) |
The order to acidity is ______.
Give the structure of the product you would expect when the following alcohol reacts with HBr.
Butan-1-ol
Give the structure of the product you would expect when the following alcohol reacts with SOCl2.
Butan-1-ol









