



In SN1 reactions, the rate-determining step is the departure of the leaving group. In the case of aromatic compounds, a resonance-stabilized carbocation can form if the leaving group is attached to the ring, which makes the reaction faster. Hence, the phenyl bromide (C6H5Br) undergoes the reaction most rapidly.
Match the Compounds (List - I) with the appropriate Catalyst/Reagents (List - II) for their reduction into corresponding amines. 
Consider the following amino acid: 
Which of the following options contain the correct structure of (A) and (B)?

Draw a rough sketch for the curve $y = 2 + |x + 1|$. Using integration, find the area of the region bounded by the curve $y = 2 + |x + 1|$, $x = -4$, $x = 3$, and $y = 0$.