The acidity of compound I is due to delocalization in the conjugate base.
The conjugate base of compound IV is aromatic.
Compound II becomes more acidic, when it has a -NO2 substituent.
The acidity of compounds follows the order I >IV>V>II>III.
A. is a conjugate base of compound I Which is stabilized by delocalization or resonance.
B. is a conjugate base of, which is an aromatic compound.
C. –NO2 group is a strong electron-withdrawing group, which increases the acidic strength of compound II.
D. The order of acidic strength.
The order of acidity of the following compounds is:
(i) o-Nitrophenol
(ii) Phenol
(iii) o-Cresol
(iv) Ethanol
Given below are two statements:
Statement I: Dimethyl ether is completely soluble in water. However, diethyl ether is soluble in water to a very small extent.
Statement II: Sodium metal can be used to dry diethyl ether and not ethyl alcohol.
In the light of the given statements, choose the correct answer from the options given below:
Two identical concave mirrors each of focal length $ f $ are facing each other as shown. A glass slab of thickness $ t $ and refractive index $ n_0 $ is placed equidistant from both mirrors on the principal axis. A monochromatic point source $ S $ is placed at the center of the slab. For the image to be formed on $ S $ itself, which of the following distances between the two mirrors is/are correct: