Step 1: Bromination of the amino group on the aromatic ring will lead to the formation of a bromo-phenyl group at the para position with respect to the amino group.
Step 2: The reaction with aqueous KOH will induce nucleophilic substitution, replacing the bromine with a hydrogen atom.
Therefore, the final product is Ph–CH2–H (option B).
Thus, the correct answer is B
The correct option is (B) :
One mole of a monoatomic ideal gas starting from state A, goes through B and C to state D, as shown in the figure. Total change in entropy (in J K\(^{-1}\)) during this process is ...............
The number of chiral carbon centers in the following molecule is ...............
A tube fitted with a semipermeable membrane is dipped into 0.001 M NaCl solution at 300 K as shown in the figure. Assume density of the solvent and solution are the same. At equilibrium, the height of the liquid column \( h \) (in cm) is .........
An electron at rest is accelerated through 10 kV potential. The de Broglie wavelength (in A) of the electron is .............